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REVIEW article

Front. Immunol., 21 January 2014
Sec. NK and Innate Lymphoid Cell Biology
This article is part of the Research Topic Molecular mechanisms regulating cytotoxic lymphocyte development and function, and their associations to human diseases. View all 18 articles

Human immunodeficiency syndromes affecting human natural killer cell cytolytic activity

  • 1Department of Immunology, College of Medicine, Mayo Clinic, Rochester, MN, USA
  • 2Division of Oncology Research and Schulze Center for Novel Therapeutics, College of Medicine, Mayo Clinic, Rochester, MN, USA

Natural killer (NK) cells are lymphocytes of the innate immune system that secrete cytokines upon activation and mediate the killing of tumor cells and virus-infected cells, especially those that escape the adaptive T cell response caused by the down regulation of MHC-I. The induction of cytotoxicity requires that NK cells contact target cells through adhesion receptors, and initiate activation signaling leading to increased adhesion and accumulation of F-actin at the NK cell cytotoxic synapse. Concurrently, lytic granules undergo minus-end directed movement and accumulate at the microtubule-organizing center through the interaction with microtubule motor proteins, followed by polarization of the lethal cargo toward the target cell. Ultimately, myosin-dependent movement of the lytic granules toward the NK cell plasma membrane through F-actin channels, along with soluble N-ethylmaleimide-sensitive factor attachment protein receptor-dependent fusion, promotes the release of the lytic granule contents into the cleft between the NK cell and target cell resulting in target cell killing. Herein, we will discuss several disease-causing mutations in primary immunodeficiency syndromes and how they impact NK cell-mediated killing by disrupting distinct steps of this tightly regulated process.

Introduction

Natural killer (NK) cells comprise 5–15% of human peripheral blood lymphocytes and play an important role in the clearance of virally infected cells, as well as the elimination of cancer cells (1, 2). The main population of NK cells differentiates from hematopoietic stem cells in the bone marrow, and fully matures as CD56+CD16+ NK cells in secondary lymphoid organs (3). While several recent studies have elegantly demonstrated the presence of a memory immune response in NK cells, previously only attributed to T and B cells of the adaptive immune system (4, 5), NK cells are generally recognized as innate immune cells by the fact that their receptors do not undergo DNA rearrangement processes. Instead NK cells express various germline-encoded activating and inhibitory NK receptors on their cell surface (68). Integrated signaling from both activating and inhibitory receptors is thought to enable NK cells to distinguish healthy “self” from infected or stressed unhealthy or “non-self” cells (9, 10). Therefore, activation of NK cells can be achieved via the ligation of a number of activating receptors with their corresponding ligand on the target cell (natural cytotoxicity). In addition, NK cells are also able to detect antibody-coated targets through the low affinity Fc receptor CD16 (FcγRIIIA) and thereby mediate antibody-dependent cellular cytotoxicity (ADCC) (11, 12). The main consequence of NK cell activation is the direct killing of bound unhealthy target cells through the release of perforin and granzymes from a preformed secretory lysosome known as the lytic granule (13, 14). In addition, NK cells can affect the overall immune response through the secretion of chemokines and cytokines (3, 1518) as well as through direct interaction with other immune cells (2, 5).

Research conducted over the past quarter of a century has uncovered the process of NK cell development, identified and demonstrated the function of activating and inhibitory receptors, and provided a wealth of information regarding the signaling pathways that are linked to these receptors and the proteins that are critical to the delivery of the lethal cargo to the target cell. Significantly, the study of human primary immunodeficiency syndromes (PIDs) has provided invaluable knowledge and insight regarding the role of NK cells in the immune system, and in addition has also resulted in the identification of genes whose protein products regulate distinct steps that are critical to the development of cellular cytotoxicity by this population of innate immune cells. Among the PIDs, several NK cell deficiencies have been identified including rare isolated NK cell deficiencies, where there is total absence or very low number of NK cells in the peripheral blood, which is known as classical natural killer cell deficiency (CNKD) (19, 20). MCM4 and GATA2 are the only two genes identified thus far in which mutations are linked to CNKD, however there remain several cases of CNKD where the underlying genetic cause has not been identified (20). Clearly, sequencing of the genomes in patients with CNKD, which are not caused by mutation of either MCM4 or GATA2, will undoubtedly reveal other genes that play an important role in NK cell development or survival.

The term NK cell deficiency does not just mean an absence of NK cells in the immune system; it also includes the absence of specific NK cell effector functions, like cytotoxicity, despite the presence of normal NK cell numbers. This has been termed functional NK cell deficiency (FNKD) (19, 20). FNKDs have provided us with very valuable insights into the roles of specific NK cell functions in immunity as well as essential proteins required for NK cell effector activities, when the responsible gene has been identified. So far, the only known human genetic mutation leading to FNKD is in the FCGR3A gene, which encodes CD16 (20, 21). Similar to patients of CNKD, patients carrying homozygous missense mutations in CD16 (L66H) showed susceptibility to human papilloma virus (HPV) or herpesviridae members. In contrast to CKND, these patients had normal numbers of NK cells, but unexpectedly showed normal ADCC, whereas natural cytotoxicity was defective (20). The fact that the altered amino acid found in these patients is located outside of the immunoglobulin domain (Ig domain) responsible for IgG binding (22) suggests why ADCC of NK cells from the patients is normal. In addition, novel co-stimulatory roles of CD16 mediated by the distal Ig domain of CD16 (23) provided important insights that might explain why the patients’ NK cells showed defective natural cytotoxicity.

Lastly, there are several additional human PIDs that demonstrate defects in NK cell numbers and effector functions. Since many immune cells other than NK cells are also affected, there are additional complications and difficulties in understanding the complex immunological roles of NK cells in these diseases. However, the identification of specific gene mutations has illuminated molecular pathways that are important for NK cell development and effector functions, which are also shared in other immune cell types. In this review, we will specifically focus on PIDs where the mutated gene products impact the intracellular pathways that regulate the development of NK cell-mediated cytotoxicity (Table 1). For detailed discussions about human diseases involved in NK cell development and differentiation, NK cell signaling, or other NK cell effector functions, the reader is referred to other excellent reviews on these topics (1921, 24).

TABLE 1
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Table 1. Human primary immunodeficiency syndromes with defective NK cell cytotoxicity.

Biogenesis of Lytic Granules and Their Maturation

Cell-mediated killing by NK cells and cytotoxic T lymphocytes (CTLs) is achieved by directed release of lytic granules toward bound target cells. Lytic granules are dual-function organelles that exhibit characteristics of a degradative lysosome, but can also secrete granule constituents for cell-mediated killing and are therefore often referred to as a secretory lysosome. This specialized organelle is mostly observed in hematopoietic lineage cells, but it is also found in melanocytes that produce pigment proteins called melanins (25, 26). Both secretory lysosomes and conventional lysosomes are acidic organelles (pH 5.1–5.4), morphologically similar, and contain proteins like acid hydrolases that are required for their degradative function as well as receptor proteins including members of the lysosomal-associated membrane protein (LAMP) family. On the other hand, the main distinction of secretory lysosomes from conventional lysosomes is that secretory lysosomes undergo a regulated secretion process and they contain additional contents that are cell-type-specific. In the case of NK cells and CTLs, these specific secreted contents include perforin and granzymes, which are essential for cytotoxic activity. On the other hand, the main secreted proteins of melanocytes are melanins, which are pigments responsible for skin color. Cells containing secretory lysosomes use common secretory machineries, but cell-type-specific secreted contents enable each cell type to perform different effector functions. This is why human genetic diseases such as Chediak–Higashi syndrome (CHS) and type 2 Hermansky–Pudlak syndrome (HPS), caused by impaired function of the secretory lysosome, are characterized not only by severe immune deficiencies including defective cytotoxicity by NK cells and CTLs but also by hypopigmentation due to defects in melanosome formation and excessive bleeding due to the absence of dense granules in platelets (2628).

In contrast to CTLs, which need to be activated, the genes encoding perforin and granzymes are constitutively transcribed in NK cells thus allowing them to immediately kill an infected or stressed cell upon initial contact and without the need for additional gene expression (29, 30). Perforin is essential for NK cell-mediated cytotoxicity, since it is the only molecule that delivers apoptosis-inducing granzymes into the target cell. Perforin is initially synthesized as an inactive precursor in the ER and undergoes multiple posttranslational modifications including proteolysis and glycosylation during its transit to the Golgi and finally to the lytic granule (31). However, the exact pathway that sorts perforin from the trans-Golgi network (TGN) into lytic granules is unresolved. After arriving into lytic granules, perforin is further processed by cathepsin L to develop into a mature form. In the case of granzymes, five different granzymes, granzyme A, B, H, K, and M, are expressed in human NK cells and CTLs. They are synthesized as pro-enzymes and modified to have a mannose-6-phosphate moiety in the cis-Golgi, which facilitates their trafficking to the endosome by the mannose-6-phosphate receptor (M6PR) before finally arriving into the lytic granule (32, 33). In lytic granules, granzymes are further processed into an active form by various cathepsins (3436). Granzymes are serine proteases and each granzyme has different substrate specificity and induces apoptosis in the target cell in both caspase-dependent and caspase-independent manners (37, 38).

An important question to be asked is: How do cytotoxic lymphocytes protect themselves from these dangerous molecules? Significantly, the activity of perforin is achieved by the membrane attack complex/perforin (MACPF) domain, which has cytolytic activity, and a C2 domain that enables binding to membrane in a calcium-dependent manner (37, 39, 40). Importantly, the low level of Ca2+ in lytic granules maintains perforin in an inactive conformation. In addition, calreticulin, another component of the lytic granule, inhibits perforin activity (41), and the acidic environment of lytic granules provides protection to NK cells since the activity of both perforin and granzymes are inhibited at this low pH. Furthermore, the low pH environment favors association of serglycin, a proteoglycan matrix found within lytic granules, with both perforin and granzymes. This interaction keeps both perforin and granzymes in an inactive state until they are secreted into a neutral pH environment (42). Interestingly, the mechanism by which perforin facilitates the transport of granzymes into the target cell is still unclear (37, 40). According to the prevailing model, perforin is released into the cytotoxic synaptic cleft where it binds calcium, oligomerizes on the target membrane, and forms pores. The high concentration of calcium as well as the neutral pH at the interface between NK cells and target cells relieves perforin from its inhibited conformation and triggers its activity (40). It is assumed that the established pore is large enough for granzymes to get into target cells by simple diffusion (21, 37, 40). Last but not least, how do NK cells prevent themselves from potential self-destruction from released cytotoxic components? Cell surface expression of cathepsin B has been suggested to provide protection of cytotoxic lymphocytes by cleaving perforin (43). In addition, it was recently shown that the surface expression of LAMP-1 (CD107a) also protects NK cells from degranulation-associated damage by inhibiting binding of perforin to NK cells (44). Therefore, it seems there exist multiple layers of protection at the final degranulation step that ensure unidirectional cytotoxicity. In the following paragraphs, we will focus our discussion on PIDs with impaired NK cell cytotoxicity caused by: (1) defects in the contents of lytic granules and (2) impaired biogenesis and maturation of lytic granules.

PIDs Affecting Contents of Lytic Granules

Familial hemophagocytic lymphohistiocytosis type 2

Familial hemophagocytic lymphohistiocytosis type 2 (FHL2) is an autosomal recessive disorder comprising 13–58% of all FHL cases and is caused by mutation of the PFR1 gene, which encodes perforin (45). Most of the mutations identified in FHL2 patients occur within regions critical for perforin maturation, or impair proper folding, oligomerization, or Ca2+-mediated membrane binding (31, 46). Interestingly, each mutation can dramatically impact the level of mature perforin, ranging from absent to normal. Additionally, the intrinsic activities of the mutated perforin correlate with the age of FHL onset and the severity of the disease (4752). Significantly, the inability of the mutated perforin to form pores on target cell membranes results in the absence of cytotoxic function of NK cells from FHL2 patients. Perforin loss did not affect the level of other lytic granule components (granzymes and cathepsins) or the steps leading to lytic granule polarization and membrane fusion (45, 53). Therefore, the normal degranulation (examined by surface expression of CD107) observed in NK cells from FHL2 patients provides us an important criterion to distinguish FHL2 patients from FHL patients caused by mutation of other genes (53). In many cases, FHL2 patients usually further develop other diseases including leukemia, juvenile rheumatoid arthritis, and macrophage activation syndrome (48, 5461), suggesting an important role for perforin and cytotoxic activity mediated by NK cells and CD8+ T cells in limiting or preventing these diseases. In addition, the non-redundant role of perforin activity in cellular cytotoxicity suggests the intervention of perforin activity as a potential therapeutic target in human diseases caused by abnormal cytotoxicity of cytotoxic lymphocytes (52).

Papillon–Lefèvre syndrome

Papillon–Lefèvre syndrome (PLS) is a rare autosomal recessive disease caused by mutation of the gene encoding cathepsin C, CTSC (6264). This disease is clinically characterized by palmoplantar keratosis, early onset of severe periodontitis, and susceptibility to viral infections. Cathepsin C is a lysosomal cysteine protease, which is responsible for the processing of granzyme A and B (36, 65). Consequently, NK cells from PLS patients primarily contain immature granzyme B, and hence, their NK cells show impaired cytotoxic activity (34). Interestingly, the impaired processing of granzyme B as well as the defective cytotoxicity could be restored by treatment of interleukin-2 (IL-2), suggesting that an IL-2 signaling pathway is able to process granzyme B in a cathepsin C-independent manner (34, 66).

PIDs Affecting Biogenesis and Maturation of Lytic Granules

Hermansky–Pudlak syndrome type 2

Hermansky–Pudlak syndrome is an autosomal recessive disease clinically characterized by oculocutaneous albinism and excessive bleeding (67, 68). Among the currently identified nine different types of HPS, Hermansky–Pudlak syndrome type 2 (HPS2) is the only type known to cause immunodeficiency in addition to other clinical symptoms (67, 69, 70). HPS2 is caused by mutation of the AP3B1 gene that encodes the β3A-subunit of adaptor protein 3 (AP3), which is part of a heterotetrameric protein complex (67, 71). Mutations leading to the loss of the β3A-subunit affect the stability of other subunits and thereby induce loss of the entire complex (67). The AP3 complex mediates sorting of integral membrane proteins from the endosome and TGN to the lysosome and secretory lysosome (72, 73). Considering the ubiquitous expression of AP3, it is very interesting to note that its absence causes severe functional defects only in cells with secretory lysosomes, indicating that AP3 is required for the biogenesis of secretory lysosomes and/or in sorting of secretory lysosome-specific proteins.

In the case of melanocytes, the AP3 complex was shown to be responsible for sorting of tyrosinase, a protein required for melanin synthesis, into the melanosome (74). Additionally, AP3-deficiency was shown to cause defective cytotoxicity of both NK cells and CTLs (17, 7577). While perforin levels in CTLs have been reported to be within the normal range in some patients with HPS2 (76), NK cells from two siblings with HPS2 showed less intracellular perforin levels compared to NK cells from healthy controls (75), suggesting that the defective NK cell-mediated cytotoxicity observed in these patients is at least partially a result of diminished perforin. Considering the fact that these patients had similar mRNA expression of perforin, correct sorting of existing perforin into lysosomes and the existence of mature perforin in patient NK cells, perforin biosynthesis seems to be independent of AP3 complex (75). Yet it remains possible that the AP3 complex is involved in sorting of proteins critical for perforin stability once perforin has made it into the lytic granule. This discrepancy between CTLs and NK cells from these patients might be due to further cell-type-specific roles of AP3 between NK cells and CTLs since lytic granule biogenesis is known to be different between these two cell types; lytic granules are preformed in resting NK cells, whereas lytic granules are generated after activation in CTLs (7880). Clearly more patients need to be accumulated to better understand these different observations. It is also interesting to note that enlarged lytic granules were observed in CTLs of HPS2 patients (77). Further elucidation of the AP3 complex target proteins required for lytic granule sorting as well as other potential roles of the AP3 complex in the biogenesis of lytic granules will be able to answer these questions.

Lastly, Clark et al. suggested that the AP3 complex might also play a more direct role(s) in the cytotoxic process of CTLs. They observed that lytic granules from AP3-deficient CTLs fail to cluster around the microtubule-organizing center (MTOC) when conjugated with appropriate target cells (77). This seems to be due to a failure of lytic granules to move along the microtubules or an inability to attach to microtubules. In addition, it is not clear whether this observed defect is a result of a direct role for AP3 in mediating lytic granule clustering at the MTOC, or due to a sorting failure of a protein(s) critical for attachment and/or movement of lytic granules along microtubules. Definitely, future studies elucidating the mechanism resulting in the phenotypes of AP3-deficiency in CTLs and NK cells will be very exciting.

Chediak–Higashi syndrome

Chediak–Higashi syndrome is another disease caused by defective lytic granule generation in NK cells and CTLs. The disease is inherited in an autosomal recessive manner and the main clinical symptoms of CHS are partial albinism and recurrent infections in the lung and skin. Mild coagulation defects and varying degrees of neurologic dysfunctions are also commonly observed in CHS patients. Although patients are often able to clear bacterial infections with the help of antibiotics, they instead develop an accelerated phase of hemophagocytic lymphohistiocytosis; seen by infiltration of macrophages and lymphocytes into the major organs of the body (81). Clinically, CHS and Griscelli syndromes (GSs; discussed in later section) present with identical features. However, at the cellular level, CHS can be distinguished from GS by the fact that CHS cells contain abnormally enlarged lysosomes and secretory lysosomes. Therefore, this cellular feature is used as the key diagnostic criterion of CHS (8284). In 1996, the responsible gene for CHS was mapped to CHS1/LYST gene (beige gene in the mouse model of CHS) (85, 86). The CHS1/LYST gene is highly conserved in all species, and a unique region at the C-terminal end of the protein called the BEACH (Beige and Chediak) motif defines a family of proteins homologous to the CHS1/LYST protein. Our current understanding suggests that all BEACH family proteins participate in vesicle trafficking (83, 87).

CHS1/LYST proteins are expressed at very low levels in all cell types, and are involved in maintaining the morphology of lysosomes and secretory lysosomes (83). However, similar to HPS2, only cells with secretory lysosome function are impaired (83, 88). In fact, although few in number, giant lytic granules are observed in NK cells and CTLs from CHS patients, and defects in cytotoxicity of both cell types have been reported from many studies (19, 21). In the case of NK cells from CHS patients, their numbers are within normal range, but the absence of CHS1/LYST causes defects in natural cytotoxicity as well as ADCC (8995). NK cells from CHS patients are able to efficiently bind target cells suggesting that the defect in NK cell-mediated cytotoxicity is due to problems in the actual cytotoxicity process. However, detailed molecular roles of CHS1/LYST in NK cell-mediated cytotoxicity have not been reported to date. Interestingly, treatment with interferons (IFNs) increase the cytotoxic capacity of NK cells from CHS patients (92, 93, 96), suggesting that IFN signaling is able to rescue cytotoxicity defects of CHS NK cells, at least partially.

Most of our knowledge regarding the cellular functions of CHS1/LYST protein were obtained from studies of CTLs from CHS patients. Unexpectedly, while giant lysosomal organelles were observed in the patients’ cells, the biogenesis, processing, and expression level of lytic proteins such as perforin and granzymes were normal, as were their sorting into lytic granules after activation. However, as time went on, the lytic granules began to fuse together becoming giant organelles (97, 98). Based on these observations, it is likely that the CHS/LYST protein either prevents abnormal fusion between lysosomal organelles or separates lysosomal membranes after normal fusion events, thus regulating lysosomal size. Significantly, CTLs from CHS patients were unable to secrete their granules in response to TCR ligation (97), suggesting that the cytotoxicity defects observed in NK cells and CTLs from CHS patients result from an exocytosis defect. Further studies elucidating the roles of CHS1/LYST in lysosomal fusion and exocytosis as well as the roles of other BEACH family proteins will provide clearer insight into the NK and CTL phenotypes observed in patients as well as the biogenesis of lytic granules and melanosomes.

Adhesion of NK Cells to Target Cells

Natural killer cells rapidly accumulate at the site of inflammation through the stimulation of inflammatory chemokine receptors and adhesion molecules expressed on their cell surface (1). Although the roles of weak adhesion molecules like selectin family members have not been directly examined in NK cell – target cell binding, it is generally appreciated that the first step toward the development of NK cell cytotoxicity is weak integrin-mediated adhesion to target cells (99). Signals from this weak adhesion, along with the initial signaling resulting from the engagement of activating/inhibitory receptors on the NK cell with corresponding ligands on the target cell, determines whether the NK cell should detach (strong inhibitory signal) or establish a firm adhesion (strong activation signals) leading to the formation of the cytotoxic synapse (CS). Along with high affinity interactions toward their ligands, integrins were also observed to cluster at the CS of NK cells, strengthening adhesion (avidity) (100102) and promoting the scanning of target cells (Figure 1) (11, 12, 99). In addition to being an important mediator of cell–cell adhesion, integrins can serve as co-stimulatory molecules enhancing cytotoxicity signals from other activating NK receptors (103105), as well as promoting lytic granule polarization following ligand engagement (104, 106108).

FIGURE 1
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Figure 1. Regulation of NK – target cell adhesion and generation of F-actin at the cytotoxic synapse. Initial signals from the NK – target interaction recruit multiple proteins responsible for integrin-mediated adhesion and high affinity maturation as well as the accumulation of F-actin at the cytotoxic synapse (CS). Absence of either the integrin β2-subunit (CD18) or its regulator, Kindlin-3, results in leukocyte adhesion deficiency type I or type III, respectively. NK cells from both diseases present defective cytotoxicity due to failure of efficient target binding and/or defective NK cell activation. The DOCK8–WASP complex is also recruited to the NK-target interface, and a “DOCK8–CDC42– WASP” pathway is likely responsible for F-actin reorganization, which might facilitate integrin-mediated adhesion and provide the F-actin meshwork critical for organization of the CS. Absence of either DOCK8 or WASP results in primary immunodeficiency disorders and NK cells from these patients show impaired NK cytotoxic activity (see text for details).

Leukocyte Adhesion Deficiency Type I

Leukocyte adhesion deficiencies (LAD) are autosomal recessive diseases caused by mutations in the genes encoding adhesion molecules or molecules critical for processing/activation of adhesion molecules. Leukocyte adhesion deficiency type I (LAD-I) is the most common type of LAD, and is caused by mutation in the gene encoding the β2-subunit of the integrin (CD18), ITGB2 (Figure 1) (109). A variety of mutations have been found in ITGB2, which can impact the expression of CD18 as well as its ability to bind a ligand (110). The main clinical symptoms of these patients are recurrent bacterial and fungal infections in the skin and mucosa, absence of pus formation at the infection sites, and impaired healing after infection. An abnormally high number of leukocytes in the blood are also a common feature of this disease, indicative of inefficient recruitment to sites of inflammation (19, 110). Supporting the essential role of integrins in mediating cytotoxicity signaling, NK cells from LAD-I patients showed defective natural cytotoxicity as well as ADCC compared to control NK cells (111113). Although the defective cytotoxicity of patients’ NK cells seems to be mainly due to impaired adhesion to target cells, it was recently suggested that LFA-1 (CD11a/CD18) might be required for clustering of lytic granules to the MTOC after target cell binding (114). However, further studies are required to clearly conclude that impaired lytic granule convergence observed in NK cells of LAD-1 patients is due to the absence of LFA-1. It remains possible that the defect observed in LAD-I NK cells might result from impaired/delayed signaling from other NK receptors caused by defective adhesion to target cells. One study suggested that the cytotoxicity defects in LAD-I NK cells could be rescued at least partly via activation with IL-2 (115). In this regard, it is very interesting to note that activation of NK cells with only IL-2 treatment promoted clustering of lytic granules (114). How IL-2 signaling is able to rescue cytotoxicity of NK cells (adhesion to target cells or clustering of lytic granules) is unclear and will require further investigation.

Leukocyte Adhesion Deficiency Type III

Leukocyte adhesion deficiency type III (LAD-III) is caused by mutation of the FERMT3 gene, which encodes Kindlin-3 (110). Kindlin-3 is expressed only in cells of the hematopoietic lineage (116), and like talin, regulates integrin-mediated adhesion by binding directly to the integrin β-chain (Figure 1) (117, 118). Patients with LAD-III have severe recurrent infections, leukocytosis, and persistent bleeding (110). As expected from the main role of Kindlin-3 in integrin-mediated adhesion, defective integrin activation was observed in platelets, lymphocytes, and polymorphonuclear leukocytes (PMNs) derived from LAD-III patients (119125). Recently, functions of NK cells from a single female infant patient were examined (126). Interestingly, specific activating receptor-mediated cytotoxicity was defective, whereas natural cytotoxicity mediated by multiple NK receptors was normal. It was suggested that Kindlin-3 might function by lowering the signaling threshold required for NK cell activation. Clearly, more patients will be needed to further define its role in NK cell-mediated cytotoxicity. In addition, further insights into the cellular roles of Kindlin-3 in inside-out/outside-in signaling by integrins as well as elucidation of the relationship of Kindlin-3 and talin in integrin regulation will be very helpful in understanding LAD-III.

Actin Reorganization at the Cytotoxic Synapse

Essential signaling molecules like NK activating/inhibitory receptors are accumulated at the center of the interface known as the central supramolecular activation cluster (cSMAC), whereas F-actin and integrins are localized at the periphery of the interface forming a ring-shaped peripheral supramolecular activation cluster (pSMAC). Among these distinct molecular patterns at the CS, F-actin accumulation at the pSMAC is thought to be one of the early and critical events in NK cell-medicated cytotoxicity, since clustering of NK receptors as well as adhesion molecules are observed to be dependent on F-actin polymerization (13, 99, 101). Two primary immunodeficiencies causing defective F-actin accumulation at the CS of NK cells have provided some clues on how F-actin accumulation might be regulated at the CS.

Wiskott–Aldrich Syndrome

Wiskott–Aldrich syndrome (WAS) is an X-linked primary immunodeficiency disorder characterized by recurrent infections, prolonged bleeding, eczema, thrombocytopenia, and impaired cellular and humoral immunity (127, 128). The disease is caused by mutations of the WAS gene, which encodes the hematopoietically expressed WAS protein (WASP) (129, 130). Depending on the disease severity and type of mutation, WAS is further subcategorized as X-linked thrombocytopenia (XLT) or X-linked neutropenia (XLN) (127, 128). WASP is the founding member of the WASP superfamily of F-actin nucleation promoting factors (NPFs), which stimulate the formation of branched F-actin via the ubiquitously expressed Arp2/3 complex (Figure 1) (131). All members of the WASP superfamily contain a C-terminal verprolin-connecting-acidic (VCA) domain that interacts with profilin-G-actin and the Arp2/3 complex (127, 128, 132). WASP is thought to play diverse roles in immune cells including formation of the immunological synapse (IS), migration, and phagocytosis (127, 128, 132). WASP-interacting protein (WIP; discussed in the next section) constitutively stabilizes WASP in an auto-inhibited conformation (133) in which the VCA domain is stabilized through an interaction with the basic region (BR) and CDC42/RAC GTPase binding domain (GBD). Cell stimulation results in the cooperative interaction of the BR with phosphatidylinositol (4,5)-biphosphate (PIP2) and active CDC42 (CDC42–GTP) with the GBD, thereby leading to the release of the bound VCA domain so that it can bind the Arp2/3 complex and promote branched F-actin generation (134138).

Wiskott–Aldrich syndrome protein was observed to localize at the pSMAC of the CS along with F-actin in target-bound NK cells, and the roles of WASP in NK cell-mediated cytotoxicity have been examined using NK cells from WAS patients (101, 139, 140). Although the proportion of NK cells in the blood was within the normal range or higher in WAS patients, WAS NK cells showed defective natural cytotoxicity as well as ADCC (139, 140). Impaired cytotoxicity of WAS NK cells was due to inefficient conjugate formation with target cells, a failure in F-actin accumulation at the cell–cell contact site, clustering of integrins and CD2, and polarization of lytic granules at the CS (Figure 1) (101, 139, 140). Interestingly, ex vivo as well as in vivo treatment with IL-2 was able to rescue impaired cytotoxicity of WAS NK cells (139, 141). IL-2 treatment of WAS NK cells restored target binding efficiency, F-actin accumulation, and polarization of lytic granules to the CS. The IL-2-mediated rescue of the defect in WAS NK cells was found to be independent of WASP function, but dependent on another WASP family member, WAVE2 (141). These findings suggest that there exists two distinct pathways for Arp2/3-generated F-actin reorganization at the CS in NK cells, and future studies should enable the use of IL-2 as a therapy to improve clinical symptoms of WAS including severe herpes simplex virus (HSV) infection caused by defective NK cell-mediated cytotoxicity.

Activation of NK cells by target cells or stimulation of CD16 was shown to activate CDC42 in NK cells (139), and accumulating observations suggest that the spatiotemporal activation of CDC42 in NK cells is important in CS formation and cytotoxic activity (142, 143). Therefore, based on current knowledge, NK cell activation results in the generation of active CDC42 at the CS, and this leads to the activation of WASP. Activated WASP will then contribute to F-actin reorganization at the CS, which will mediate the clustering of CD2, integrins, and NK receptors. However, there are still many important questions to be answered regarding the role and regulation of WASP in NK cell-mediated cytotoxicity. For example: (1) What are the upstream signaling pathways that lead to the activation of CDC42 and the generation of PIP2 that are required for WASP activation at the CS? (2) How is WASP accumulated at the CS after the stimulation of NK cells? and (3) How does WASP mediate the polarization of lytic granules toward the CS? Future studies aimed at addressing these and other important questions will provide insight into how WASP is regulated and mechanistic insight into its role in the development of NK cell-mediated killing.

WASP-Interacting Protein Deficiency

Deficiency of WASP-interacting protein was recently identified in a female infant patient (144). The patient had a homozygous mutation in the WIPF1 gene and both of her parents were heterozygous for the same mutation, suggesting that the disease is inherited in an autosomal recessive manner. WIP is ubiquitously expressed in humans, although higher levels are observed in hematopoietic cells (145). The clinical features were very similar to those observed in WAS patients, including recurrent infections, thrombocytopenia, eczema, and immunodeficiency. This is not surprising as WIP is thought to maintain the stability of WASP and regulate WASP activity (Figure 1) (145, 146). Consistent with this, WASP protein was not detected in the patient’s T cells, despite normal WAS mRNA expression. However, several WASP-independent functions of WIP have been observed in NK cells. First of all, WIP was shown to be essential for formation of a multiprotein complex composed of WIP, WASP, actin, and myosin IIA after NK cell activation (147). WIP was also found to associate with the lytic granules in NK cells and WIP-depleted NK cells failed to polarize their lytic granules toward the CS (148). In addition, the expression level of major NK activating receptors (NKG2D, NKp30, and NKp46) was lower on WIP-deficient NK cells compared to control NK cells. These findings also suggest that patients with WAS symptoms cannot be simply diagnosed based on WASP expression at the protein level, and will require sequence analysis of the WAS and WIPF1 genes to distinguish between WAS and WIP deficiency.

Dedicator of Cytokinesis 8 Deficiency

Another PID that causes defective F-actin accumulation at the CS of NK cells is the loss of dedicator of cytokinesis 8 (DOCK8). DOCK8 is a member of the DOCK180 family of guanine nucleotide exchange factors (GEFs) that mediate activation of Rho family proteins and contribute to multiple cellular processes including cell migration and phagocytosis (149151). DOCK8 deficiency is a relatively recently identified primary combined immunodeficiency that shows an autosomal recessive pattern of inheritance (152, 153). The main clinical symptoms of these patients are recurrent infections in the lung and skin, high IgE levels in the serum, and severe allergies (152154). The roles of DOCK8 in human NK cells have been examined recently using NK cells from DOCK8-deficient patients as well as primary human NK cells and human NK cell-lines depleted of DOCK8 by RNAi (155, 156). DOCK8-deficient/depleted NK cells showed defective natural cytotoxicity and specific activating receptor-mediated NK cytotoxicity, suggesting that functional defects of NK cells in DOCK8-deficient patients could be part of the cause for the frequent sinopulmonary infections observed in these patients (152154, 157). Defective accumulation of F-actin and clustering of integrins at the IS were also observed in DOCK8-deficient/depleted NK cells as well as B cells and CD8+ T cells from DOCK8-mutant mice (155158). Polarization of lytic granules toward the CS was also defective in DOCK8-deficient/depleted NK cells (155, 156). Mechanistically, DOCK8 was found to interact with WASP and talin, and to mediate their localization to the CS of NK cells (Figure 1) (155). Significantly, DOCK8 was found to have GEF-specificity toward CDC42 (155, 159). These findings provide an important link between the signaling pathways that might activate WASP and may help explain the remarkable similarities between WAS and DOCK8 deficiency. In fact both diseases share many clinical symptoms [recurrent infections by certain types of viruses, and high IgE levels] (127, 128, 132, 152154, 157), as well as phenotypes observed in NK cells [defective cytotoxic activity, integrin-mediated adhesion, F-actin accumulation, and polarization of lytic granules (101, 139, 140, 155, 156)].

Surprisingly, the addition of IL-2 was unable to rescue the cytotoxic defects seen in DOCK8-deficient NK cell suggesting that DOCK8 is likely involved in the regulation of other signaling pathways in addition to its role in localizing and potentially activating WASP. However, based on the current findings, it is very tempting to hypothesize that DOCK8 mediates the recruitment of WASP to the CS of NK cells after activation where it can generate active CDC42 thus leading to the activation of WASP (Figure 1). Another DOCK8-interacting partner, talin, associates with phosphatidylinositol phosphate kinase type Iγ (PIPKIγ), which produces PtdIns (4,5)P2 (PIP2), a molecule required for optimal activation of WASP (134138, 160162). The activated WASP is then able to interact with Arp2/3 inducing the generation of a branched F-actin network, and this enhances the clustering of integrins and NK receptors. Future studies testing the hypothesis of the “DOCK8–CDC42–WASP” pathway should provide a clearer picture of the formation of the CS. Lastly, one remaining question regarding the role of DOCK8 and WASP is how they mediate the polarization of lytic granules toward the CS. Based on current knowledge, it is most likely that polarization of lytic granules toward the CS occurs later than F-actin accumulation (101) since cytochalasin D (Cyt D)-treated NK cells also showed defective polarization of lytic granules (140). However, considering the fact that CDC42 is best known for regulating cellular polarity and is responsible for MTOC polarization in T cells, macrophages, and dendritic cells (DCs) (163167), DOCK8 might regulate MTOC polarization through the activation of other CDC42 effector molecules in addition to regulating the CDC42–WASP pathway leading to F-actin accumulation.

Polarization of Lytic Granules toward Cytotoxic Synapse

Another important step required for NK cell-mediated cytotoxicity is the polarization of lytic granules toward the CS. This event occurs after the rearrangement of F-actin at the CS and requires both F-actin polymerization and microtubule function, since lytic granules fail to polarize toward the CS when either F-actin accumulation or the microtubule network are disrupted (101). As NK cells start to form conjugates with target cells, lytic granules are rapidly clustered around the MTOC (Figure 2) (107). This retrograde, minus-end-directed transport of lytic granules on microtubules is Src kinase-dependent, and mediated by the dynein/dynactin motor complex that constitutively associates with lytic granules and tethers them to the microtubules (107, 114, 168). In conjunction with the clustering of the lytic granules, the MTOC polarizes toward the CS, thereby delivering the lethal cargo to the site of target cell contact (101, 107, 168). Importantly, this process occurs along with maturation of the CS, as it requires F-actin accumulation, rearrangement of NK receptors, and clustering of adhesion molecules.

FIGURE 2
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Figure 2. Fusion and exocytosis of lytic granules during NK cell-mediated cytotoxicity. Directed release of lytic granules toward bound target cells is a multi-step process: (1) lytic granules are rapidly clustered around the MTOC. This retrograde (minus-end-directed) movement along the microtubules occurs rapidly and is mediated by the dynein/dynactin motor complex. (2) The MTOC, along with accumulated lytic granules, are polarized toward the CS, and several proteins have been identified to be critical for this step. (3) Polarized lytic granules are further delivered toward the CS along the microtubule (anterograde transport) in a kinesin-1-dependent manner. (4) Myosin IIA facilitates the final transit of the lytic granules through the hypodense F-actin meshwork at the CS. NK cells from patients with MYH9-related diseases fail to degranulate. (5) The final fusion of lytic granules with the plasma membrane occurs in an orchestrated manner and requires multiple molecules including Rab27a, its effector protein Munc13-4, SNARE proteins, and their accessory proteins. Mutations in proteins involved in this final fusion step have been found to cause immunodeficiency disorders including Griscelli syndrome type 2, familial hemophagocytic lymphohistiocytosis types 3, 4, and 5, all of which have similar clinical symptoms, and defective lytic granule exocytosis.

Current knowledge suggests that activation of extracellular-signal-regulated kinase (Erk), Vav1, and protein tyrosine kinase 2 (PYK2) are required for MTOC polarization in NK cells (169171). In addition to these molecules, several other proteins have been identified that impact the polarization of lytic granules to the CS (Figure 2). For example, interrupting the cellular function of the CDC42-interacting protein-4 (CIP4) was shown to impair MTOC polarization as well as NK cell-mediated cytotoxicity (172). CIP4 was suggested to link the microtubule and F-actin network at the CS through its ability to interact with microtubules and WASP. In this regard, the scaffold protein IQGAP1 also has the potential to interact with F-actin and microtubules, and silencing of IQGAP1 was also shown to impair NK cell cytotoxicity due to defective MTOC polarization toward the CS (173). However, MTOC polarization and cell-mediated killing were found to be normal in mouse CTLs lacking IQGAP1 (174), highlighting again that distinct mechanisms regulating cell-mediated killing are engaged in these two cell types. The Ral GTPase, RalA, also regulates MTOC polarization toward the CS (175). Very recently, the small GTP-binding protein, Arl8b, was found to interact with KIF5B, the heavy chain of the microtubule plus-end-directed motor kinesin-1, and mediate MTOC polarization in NK cells (176). How and where the kinesin-1 motor is recruited to mediate movement of both the MTOC and lytic granules toward the CS remains unclear. In CTLs, a Rab27a/Slp3/kinesin-1 complex was reported to be critical for final transport of polarized lytic granules along with microtubules toward the CS (Figure 2). Interestingly, polarization of the MTOC toward the CS was normal when kinesin-1 was interrupted in CTLs (177). It will be interesting to analyze these seemingly different roles of kinesin-1 in both NK cells and CTLs. Lastly, although not examined in NK cells, activity of CDC42 might also be essential for MTOC polarization considering similar roles in other immune and non-immune cells (163167).

Following the clustering of the lytic granules at the MTOC, the MTOC docks near the plasma membrane (PM) facilitating fusion of lytic granules into the secretory cleft formed between the NK cell and target cell (168, 178). Previous studies using conventional confocal microscopy suggested that the lytic granules pass through an actin-cleared region at the center of the CS (101, 102); however, recent approaches using super-resolution microscopy suggest that the secretory region at the center of the CS is not totally absent of F-actin. Instead, a hypodense branched F-actin meshwork exists in the central region of the CS that is rearranged to produce small pores through which the lytic granules travel (179, 180). The previously suggested role of myosin IIA, an actin motor protein, in the final transit of lytic granules through the actin-rich region of the CS are consistent with this new finding and will be discussed in the next section (Figure 2). It still remains to be determined how the F-actin network at the secretory region is regulated to allow lytic granule movement by the myosin motor protein.

MYH9-Related Disease

Myosin IIA is an actin-based molecular motor that promotes movement along F-actin and is known to be involved in numerous cellular processes (181). Myosin IIA is a hexameric protein composed of two heavy chains, two regulatory light chains, and two essential light chains. The heavy chain of myosin IIA contains a motor domain at the N-terminal head that binds to F-actin to perform its motor function through ATP hydrolysis, whereas the C-terminal region performs filament formation, cargo binding, and regulatory functions (182184). In humans, mutations in MYH9 gene, which encodes the heavy chain, lead to autosomal dominant diseases collectively known as MYH9-related diseases (MYH9-RDs), which include May–Hegglin Anomaly, Sebastian Syndrome, Fechtner Syndrome, and Epstein Syndromes (185, 186). The main clinical features of MYH-RD are macrothrombocytopenia and granulocyte inclusions.

Previous studies using the myosin light chain kinase inhibitor ML-9 (1-[5-chloronaphthalene-1-sulfonyl]-1H-hexahydro-1,4-diazepine) inhibited NK cell-mediated cytotoxicity (187), suggesting that myosin IIA would be critical for NK cell effector activity. Consistent with this notion, NK cells from MYH9-RD patients as well as human NK cells that were either inhibited pharmacologically or depleted of myosin IIA function had impaired NK cell-mediated cytotoxicity (188190). Molecularly, it was found that inhibition or depletion of myosin IIA did not affect the early steps of NK cytotoxicity including target binding, F-actin accumulation, or polarization of lytic granules, but caused impaired degranulation (Figure 2). It was further found that a pool of myosin IIA is associated constitutively with lytic granules, and facilitates the final transit of the lytic granules through the F-actin meshwork at the secretory region of the CS (190). It is important to note that there might be other important roles of myosin IIA in NK cell-mediated cytotoxicity. For example, as mentioned in the previous section, it was shown that myosin IIA and actin are recruited to WIP during NK cell activation (147). Lastly, a large fraction of myosin IIA is found associated with the F-actin at the cell cortex, suggesting that there are likely other functions of myosin IIA in addition to its role in regulating lytic granule trafficking at the CS (147, 188, 190). Future studies regarding other cellular roles of myosin IIA in the NK cytotoxicity and their connection with roles in lytic granule transport will be interesting.

Fusion of Lytic Granules with the Plasma Membrane

Exocytosis of lytic granules requires membrane fusion between lytic granules and the PM. An increasing number of studies suggest that small GTPases, including Rab–GTPases, known to regulate membrane trafficking and fusion are important regulators of lytic granule exocytosis in NK cells (191, 192). Following GDP to GTP exchange, these small GTPases are able to interact with their effector proteins involved in protein sorting, motor activity, and tethering, thereby impacting membrane trafficking. Therefore, they are suggested to play important roles, at least in determining specificity of the initial tethering step (Figure 2) (193, 194). In fact, mutation in Rab27a is known to be responsible for a PID known as Griscelli syndrome type 2 (GS2), which will be discussed in detail below (195, 196).

In addition to Rab proteins, the soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) proteins, which are known to mediate most membrane fusion events in eukaryotic cells, also participate in exocytosis (197199). There are approximately 40 SNARE family proteins in humans with different combinations of SNARE proteins expressed in different cell types. In addition, each SNARE protein exhibits a distinct localization pattern suggesting that selective pairings of SNARE members in specific organelles (like lytic granules) constrain their target binding (197199). All SNARE proteins contain a coiled-coil SNARE motif at the center, and are structurally categorized as either an R-SNARE or Q-SNARE (further subclassified as Qa-, Qb-, Qc-, or Qb,c-SNARE). Membrane fusion is induced when an R-SNARE protein, such as those found on the lytic granule membrane binds to its cognate Q-SNARE proteins expressed on the PM (Figure 2). Bundling of four SNARE motifs (one from the R-SNARE, and three motifs from two or three Q-SNAREs) makes a stable SNARE complex, and the exerted mechanical force pulls the two membranes closer to promote membrane fusion. Interestingly, familial hemophagocytic lymphohistiocytosis type 4 (FHL4) is the result of a mutation in the gene encoding a Qa-SNARE protein called syntaxin-11 (STX11) (200, 201). In addition to the selectivity of SNARE proteins, accessory proteins including SM (Sec1/Munc18-like), Munc13-like, and synaptotagmin associate with SNARE proteins to regulate membrane fusion both temporally and spatially (197199, 202). Mutations in Munc13-4 and Munc18-2/syntaxin-binding protein 2 (STXBP2) are responsible for familial hemophagocytic lymphohistiocytosis type 3 (FHL3) and familial hemophagocytic lymphohistiocytosis type 5 (FHL5), respectively (Figure 2) (203205). Lastly, the entry of extracellular Ca2+ is essential for lytic granule exocytosis (206). Although PIDs regarding this category are not discussed in this review (please refer to reviews (21, 207) for more details), NK cells from patients deficient in either the ER calcium sensor STIM1 or the PM calcium channel ORAI1 showed defective cytotoxicity due to impaired exocytosis of lytic granules, although polarization of lytic granules toward the CS was normal (206). Significantly, Munc13 proteins and synaptotagmin proteins contain two calcium-dependent phospholipid-binding C2 domains and are known to regulate activity of the SNARE complex in a Ca2+-regulated manner (197, 199, 202). Likewise, members of the synaptotagmin-like protein (Slp) family also share C-terminal tandem C2 domains. Slps were also shown to interact with activated Rab27 (Rab27–GTP) via the Slp homology domain (SHD) and participate in docking granules to the membrane (208). Unfortunately, we still do not have a clear picture as to which of these proteins are regulating the membrane fusion steps in NK cell-mediated cytotoxicity. However, as discussed below, clues to understanding this seemingly complicated and tightly regulated mechanism of lytic granule docking and fusion have been uncovered by functionally antagonizing these molecular pathways and examining NK cells from PID patients deficient in these key molecules.

Griscelli Syndrome Type 2

Griscelli syndrome type 2 is an autosomal recessive human disease caused by mutations in the RAB27A gene that encodes the small GTPase Rab27a (195, 196). GS2 is clinically characterized by severe immunodeficiency, an accelerated phase of HLH, partial albinism, and distinctive silvery-grayish hair (209, 210). GS2 is distinguished from other subtypes of GS (GS1: mutation in MYO5A encoding myosin Va; GS3: mutation in MLPH encoding melanophilin) from the fact that only GS2 is associated with the development of hemophagocytosis (211). Since all three responsible proteins for GS are required for distribution of melanins in melanocytes (212), hypopigmentation due to defective melanosome function is a common feature of all subtypes of GS. On the other hand, the fact that cytotoxic lymphocytes only express Rab27a among the three proteins explains why abnormal immune function is only observed in GS2 (213). NK cells from GS2 patients showed defective cytotoxicity which could be at least partially restored by treatment of IL-2 (192, 214217). In CTLs of GS2 patients as well as Rab27a mutant Ashen mice, docking of lytic granules at the PM and the subsequent degranulation process were impaired (195, 204, 218, 219). Supporting the role of Rab27a observed in CTLs, degranulation of activated NK cells from GS2 patients was defective (192), and depletion of Rab27a in the human NK cell-line, NKL, showed a decreased number of lytic granules at the PM (Figure 2) (191). As discussed above, synaptotagmin-like proteins 1–3 (Slp1–3), which are effectors of Rab27a, are expressed in CTLs and involved in lytic granule exocytosis (177, 220, 221). Interestingly, it was recently found that Slp3 interacts with the kinesin-1 motor protein. This is significant, as the motor activity of kinesin-1 was suggested to deliver the slp3/Rab27a complex toward the CS of CTLs (177). Lastly, while Rab27a is in a distinct compartment from lytic granules in both resting NK cells and CTLs (192, 222), when they are activated, Rab27a is recruited to lytic granules. Whether Rab27a binding to Slp3 or some other effector molecule mediates this recruitment remains to be determined.

Familial Hemophagocytic Lymphohistiocytosis Type 3

Familial hemophagocytic lymphohistiocytosis type 3 is caused by mutation in UNC13D, which encodes Munc13-4 (204). Like other types of FHL, FHL3 patients present with hyperactive CTLs and macrophages in the peripheral blood. Patients usually have fever, hepatosplenomegaly, defective coagulation, and features of hemophagocytosis (204, 223, 224). Initial studies of Munc13-4 function reported that Munc13-4 is highly expressed in hematopoietic cells and involved in cytotoxicity of CTLs by mediating the exocytosis of lytic granules (204). In line with this finding in CTLs, cytotoxic activities (both natural cytotoxicity and ADCC) were defective in NK cells from FHL3 patients, whereas levels of cytokines produced by activated NK cells were normal (48, 53, 225). Consistent with the defect being at the level of lytic granule fusion, the polarization of lytic granules toward the CS was normal, but the patient NK cells failed to degranulate (Figure 2) (53, 54). As indicated above, Munc13-4 contains one diacylglycerol (DAG) binding C1 domain and two Ca2+-binding C2 domains (204), suggesting it regulates SNARE conformation in Ca2+-dependent manner like other Munc13 members in a process called “priming,” which guides incomplete SNARE components for full assembly. However, it is still unclear which target SNARE proteins are regulated by Munc13-4 and how it acts mechanically during NK cell degranulation. However, one of the interesting findings to note is that Munc13-4 was found to be an effector of activated Rab27a (Rab27a–GTP) (226, 227). When NK cells become activated, both proteins were found to associate with lytic granules, and the recruitment of each protein was dependent on the other (192). It is also very intriguing to note that the recruitment of these proteins to lytic granules also requires myosin IIA, since inhibition of myosin activity blocked their recruitment (192). Clearly much more work is needed to delineate the mechanisms by which Rab27a and Munc13-4 regulate lytic granule docking and fusion.

Familial Hemophagocytic Lymphohistiocytosis Type 4

Familial hemophagocytic lymphohistiocytosis type 4 is caused by mutations in the gene that encodes the Qa-SNARE protein STX11 (200, 201). STX11 is considered an atypical member of the syntaxin family, since it lacks the hydrophobic transmembrane domain found in other syntaxin family members that is involved in membrane binding (228). Instead, STX11 is able to associate with membranes via a cysteine-rich region located at its C-terminal end (229). NK cells from FHL4 patients or human NK cells depleted of STX11 showed defects in both natural cytotoxicity and specific activating receptor-mediated cytotoxicity (54, 230). Polarization of lytic granules toward the CS was normal in these NK cells, but they failed to degranulate suggesting the roles of STX11 in the late step of lytic granule release (Figure 2). Recently established STX11-deficient mice also support findings from the patients (231, 232). Interestingly, the NK cell defects from FHL4 patients were partly rescued with IL-2 treatment (54). It is of interest that STX11 localizes to the late endosome and the TGN (233, 234). Over-expressed STX11 also showed a distinct localization pattern that was different from both Rab27a and perforin in resting NKLs, but upon activation, they colocalized with each other at the CS. It is unclear why these proteins (Rab27a, Munc13-4, and STX11) exist in distinct subcellular compartments prior to activation, but one possible explanation would be the separation of exocytic machineries and lytic granules in the resting state to prevent premature granule exocytosis. Another important issue remaining to be resolved is the identification of the other SNARE complex members that contribute to membrane fusion. Two R-SNARE proteins, VAMP4 and VAMP7, were recently shown to colocalize with perforin in activated NK cells, and mediate lytic granule exocytosis (235, 236). The Qb,c-SNARE protein, SNAP23, is known to interact with STX11 in B cells; therefore, it is intriguing to hypothesize that it might also mediate degranulation of lytic granules in NK cells in cooperation with STX11. STX11 was also identified to interact with Munc18-2/STXBP2, which might play important roles in priming the SNARE complex containing STX11 (203, 205).

Familial Hemophagocytic Lymphohistiocytosis Type 5

Familial hemophagocytic lymphohistiocytosis type 5 is a recently identified type of FHL caused by mutation in STXBP2, which encodes Munc18-2 (also called STXBP2) (203, 205). FHL5 patients have either a very low level of Munc18-2 or no expression due to homozygous or compound heterozygous mutations in the STXBP2 gene. In addition to common clinical features of FHL, some FHL5 patients additionally presented with colitis, bleeding disorders, and hypogammaglobulinemia (210, 224). Munc18-2 is a member of the SM (Sec1/Munc18-like) protein family, and likely guides appropriate SNAREs for productive complex formation (197199, 202). Interestingly, Munc18-2 was found to colocalize and interact with STX11 and the protein expression level of STX11 seems to correlate with that of Munc18-2. However, the absence of STX11 did not affect Munc18-2 protein levels suggesting that Munc18-2 might be the main SM protein regulating the STX11 SNARE complex (203). Importantly, NK cells from these patients presented with impaired cytotoxic activity due to defective degranulation (Figure 2) (203, 205, 224, 237). Interestingly, similar to what has been observed in NK cells from FHL4 patients, IL-2 stimulation of NK cells from FHL5 patients partially rescued the cytotoxicity defects, suggesting that the IL-2 pathway is able to bypass the defective Munc18-2/STX11 pathway in both FHL4 and FHL5.

Conclusion

Advances in clinical diagnostics has substantially increased the identification of patients with PIDs that affect NK cell numbers or effector functions. In addition to furthering our understanding of NK cells in the immune system (CKND and FKND), this group of diseases has substantiated the important roles that NK cells play in immune surveillance. Furthermore, the quantitative and/or qualitative defects in NK cells derived from these patients have highlighted essential molecular machineries shared among immune cells and their importance in NK cell-mediated cytotoxicity. In fact, these loss-of-function mutations have provided invaluable insight into the molecular processes regulating the development of cell-mediated killing by NK cells. However, there are many issues that still remain unanswered. First, how can IL-2-mediated signaling pathways restore NK cell functions in multiple PIDs? Secondly, what are the NK cell-specific mechanisms that differentiate the cytotoxic processes engaged in NK cells from those of CTLs (from biogenesis to exocytosis of lytic granules)? Lastly, how do the signaling molecules that regulate the detailed secretory pathway of lytic granules in NK cells cooperate with the multiple tethering and fusion molecules to promote lytic granule exocytosis? It is clear that PIDs have substantially impacted our understanding of NK cell biology and the cellular mechanisms that control the tightly regulated process of lytic granule release. Further mechanistic insight into the process of NK cell-mediated killing will hopefully reveal novel therapeutic approaches to treat PID patients.

Conflict of Interest Statement

The authors declare that the research was conducted without any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

This work was supported by the Mayo Foundation, Mayo Graduate School and National Cancer Institute Grant R01 CA47752 to Daniel D. Billadeau.

References

1. Gregoire C, Chasson L, Luci C, Tomasello E, Geissmann F, Vivier E, et al. The trafficking of natural killer cells. Immunol Rev (2007) 220:169–82. doi:10.1111/j.1600-065X.2007.00563.x

CrossRef Full Text

2. Vivier E, Tomasello E, Baratin M, Walzer T, Ugolini S. Functions of natural killer cells. Nat Immunol (2008) 9(5):503–10. doi:10.1038/ni1582

CrossRef Full Text

3. Caligiuri MA. Human natural killer cells. Blood (2008) 112(3):461–9. doi:10.1182/blood-2007-09-077438

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

4. Paust S, von Andrian UH. Natural killer cell memory. Nat Immunol (2011) 12(6):500–8. doi:10.1038/ni.2032

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

5. Vivier E, Raulet DH, Moretta A, Caligiuri MA, Zitvogel L, Lanier LL, et al. Innate or adaptive immunity? The example of natural killer cells. Science (2011) 331(6013):44–9. doi:10.1126/science.1198687

CrossRef Full Text

6. Bryceson YT, Long EO. Line of attack: NK cell specificity and integration of signals. Curr Opin Immunol (2008) 20(3):344–52. doi:10.1016/j.coi.2008.03.005

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

7. Lanier LL. NK cell recognition. Annu Rev Immunol (2005) 23:225–74. doi:10.1146/annurev.immunol.23.021704.115526

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

8. Watzl C, Urlaub D. Molecular mechanisms of natural killer cell regulation. Front Biosci (Landmark Ed) (2012) 17:1418–32. doi:10.2741/3995

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

9. Karre K. Natural killer cell recognition of missing self. Nat Immunol (2008) 9(5):477–80. doi:10.1038/ni0508-477

CrossRef Full Text

10. Raulet DH. Missing self recognition and self tolerance of natural killer (NK) cells. Semin Immunol (2006) 18(3):145–50. doi:10.1016/j.smim.2006.03.003

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

11. Bryceson YT, Chiang SC, Darmanin S, Fauriat C, Schlums H, Theorell J, et al. Molecular mechanisms of natural killer cell activation. J Innate Immun (2011) 3(3):216–26. doi:10.1159/000325265

CrossRef Full Text

12. Watzl C, Long EO. Signal transduction during activation and inhibition of natural killer cells. Curr Protoc Immunol (2010) Chapter 11:Unit 11.9B. doi:10.1002/0471142735.im1109bs90

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

13. Dustin ML, Long EO. Cytotoxic immunological synapses. Immunol Rev (2010) 235(1):24–34. doi:10.1111/j.0105-2896.2010.00904.x

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

14. Stinchcombe JC, Griffiths GM. Secretory mechanisms in cell-mediated cytotoxicity. Annu Rev Cell Dev Biol (2007) 23:495–517. doi:10.1146/annurev.cellbio.23.090506.123521

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

15. Biron CA, Nguyen KB, Pien GC, Cousens LP, Salazar-Mather TP. Natural killer cells in antiviral defense: function and regulation by innate cytokines. Annu Rev Immunol (1999) 17:189–220. doi:10.1146/annurev.immunol.17.1.189

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

16. Fauriat C, Long EO, Ljunggren HG, Bryceson YT. Regulation of human NK-cell cytokine and chemokine production by target cell recognition. Blood (2010) 115(11):2167–76. doi:10.1182/blood-2009-08-238469

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

17. Munz C. Non-cytotoxic protection by human NK cells in mucosal secondary lymphoid tissues. Eur J Immunol (2008) 38(11):2946–8. doi:10.1002/eji.200838849

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

18. Strowig T, Brilot F, Munz C. Noncytotoxic functions of NK cells: direct pathogen restriction and assistance to adaptive immunity. J Immunol (2008) 180(12):7785–91.

Pubmed Abstract | Pubmed Full Text

19. Orange JS. Human natural killer cell deficiencies and susceptibility to infection. Microbes Infect (2002) 4(15):1545–58. doi:10.1016/S1286-4579(02)00038-2

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

20. Orange JS. Natural killer cell deficiency. J Allergy Clin Immunol (2013) 132(3):515–25; quiz 26. doi:10.1016/j.jaci.2013.07.020

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

21. Wood SM, Ljunggren HG, Bryceson YT. Insights into NK cell biology from human genetics and disease associations. Cell Mol Life Sci (2011) 68(21):3479–93. doi:10.1007/s00018-011-0799-y

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

22. Tamm A, Schmidt RE. The binding epitopes of human CD16 (Fc gamma RIII) monoclonal antibodies. Implications for ligand binding. J Immunol (1996) 157(4):1576–81.

Pubmed Abstract | Pubmed Full Text

23. Grier JT, Forbes LR, Monaco-Shawver L, Oshinsky J, Atkinson TP, Moody C, et al. Human immunodeficiency-causing mutation defines CD16 in spontaneous NK cell cytotoxicity. J Clin Invest (2012) 122(10):3769–80. doi:10.1172/JCI64837

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

24. Orange JS. Human natural killer cell deficiencies. Curr Opin Allergy Clin Immunol (2006) 6(6):399–409. doi:10.1097/ACI.0b013e3280106b65

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

25. Blott EJ, Griffiths GM. Secretory lysosomes. Nat Rev Mol Cell Biol (2002) 3(2):122–31. doi:10.1038/nrm732

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

26. Clark R, Griffiths GM. Lytic granules, secretory lysosomes and disease. Curr Opin Immunol (2003) 15(5):516–21. doi:10.1016/S0952-7915(03)00113-4

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

27. Dell’Angelica EC, Mullins C, Caplan S, Bonifacino JS. Lysosome-related organelles. FASEB J (2000) 14(10):1265–78. doi:10.1096/fj.14.10.1265

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

28. Griffiths GM. Albinism and immunity: what’s the link? Curr Mol Med (2002) 2(5):479–83. doi:10.2174/1566524023362258

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

29. Nakata M, Kawasaki A, Azuma M, Tsuji K, Matsuda H, Shinkai Y, et al. Expression of perforin and cytolytic potential of human peripheral blood lymphocyte subpopulations. Int Immunol (1992) 4(9):1049–54. doi:10.1093/intimm/4.9.1049

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

30. Salcedo TW, Azzoni L, Wolf SF, Perussia B. Modulation of perforin and granzyme messenger RNA expression in human natural killer cells. J Immunol (1993) 151(5):2511–20.

Pubmed Abstract | Pubmed Full Text

31. Uellner R, Zvelebil MJ, Hopkins J, Jones J, MacDougall LK, Morgan BP, et al. Perforin is activated by a proteolytic cleavage during biosynthesis which reveals a phospholipid-binding C2 domain. EMBO J (1997) 16(24):7287–96. doi:10.1093/emboj/16.24.7287

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

32. Griffiths GM, Isaaz S. Granzymes A and B are targeted to the lytic granules of lymphocytes by the mannose-6-phosphate receptor. J Cell Biol (1993) 120(4):885–96. doi:10.1083/jcb.120.4.885

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

33. Bossi G, Griffiths GM. CTL secretory lysosomes: biogenesis and secretion of a harmful organelle. Semin Immunol (2005) 17(1):87–94. doi:10.1016/j.smim.2004.09.007

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

34. Meade JL, de Wynter EA, Brett P, Sharif SM, Woods CG, Markham AF, et al. A family with Papillon-Lefevre syndrome reveals a requirement for cathepsin C in granzyme B activation and NK cell cytolytic activity. Blood (2006) 107(9):3665–8. doi:10.1182/blood-2005-03-1140

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

35. D’Angelo ME, Bird PI, Peters C, Reinheckel T, Trapani JA, Sutton VR. Cathepsin H is an additional convertase of pro-granzyme B. J Biol Chem (2010) 285(27):20514–9. doi:10.1074/jbc.M109.094573

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

36. Smyth MJ, McGuire MJ, Thia KY. Expression of recombinant human granzyme B. A processing and activation role for dipeptidyl peptidase I. J Immunol (1995) 154(12):6299–305.

Pubmed Abstract | Pubmed Full Text

37. Krzewski K, Coligan JE. Human NK cell lytic granules and regulation of their exocytosis. Front Immunol (2012) 3:335. doi:10.3389/fimmu.2012.00335

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

38. Grossman WJ, Revell PA, Lu ZH, Johnson H, Bredemeyer AJ, Ley TJ. The orphan granzymes of humans and mice. Curr Opin Immunol (2003) 15(5):544–52. doi:10.1016/S0952-7915(03)00099-2

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

39. Voskoboinik I, Thia MC, Fletcher J, Ciccone A, Browne K, Smyth MJ, et al. Calcium-dependent plasma membrane binding and cell lysis by perforin are mediated through its C2 domain: a critical role for aspartate residues 429, 435, 483, and 485 but not 491. J Biol Chem (2005) 280(9):8426–34. doi:10.1074/jbc.M413303200

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

40. Lopez JA, Brennan AJ, Whisstock JC, Voskoboinik I, Trapani JA. Protecting a serial killer: pathways for perforin trafficking and self-defence ensure sequential target cell death. Trends Immunol (2012) 33(8):406–12. doi:10.1016/j.it.2012.04.001

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

41. Fraser SA, Karimi R, Michalak M, Hudig D. Perforin lytic activity is controlled by calreticulin. J Immunol (2000) 164(8):4150–5.

Pubmed Abstract | Pubmed Full Text

42. Masson D, Peters PJ, Geuze HJ, Borst J, Tschopp J. Interaction of chondroitin sulfate with perforin and granzymes of cytolytic T-cells is dependent on pH. Biochemistry (1990) 29(51):11229–35. doi:10.1021/bi00503a011

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

43. Balaji KN, Schaschke N, Machleidt W, Catalfamo M, Henkart PA. Surface cathepsin B protects cytotoxic lymphocytes from self-destruction after degranulation. J Exp Med (2002) 196(4):493–503. doi:10.1084/jem.20011836

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

44. Cohnen A, Chiang SC, Stojanovic A, Schmidt H, Claus M, Saftig P, et al. Surface CD107a/LAMP-1 protects natural killer cells from degranulation-associated damage. Blood (2013) 122(8):1411–8. doi:10.1182/blood-2012-07-441832

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

45. Stepp SE, Dufourcq-Lagelouse R, Le Deist F, Bhawan S, Certain S, Mathew PA, et al. Perforin gene defects in familial hemophagocytic lymphohistiocytosis. Science (1999) 286(5446):1957–9. doi:10.1126/science.286.5446.1957

CrossRef Full Text

46. de Saint Basile G, Menasche G, Fischer A. Molecular mechanisms of biogenesis and exocytosis of cytotoxic granules. Nat Rev Immunol (2010) 10(8):568–79. doi:10.1038/nri2803

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

47. Feldmann J, Menasche G, Callebaut I, Minard-Colin V, Bader-Meunier B, Le Clainche L, et al. Severe and progressive encephalitis as a presenting manifestation of a novel missense perforin mutation and impaired cytolytic activity. Blood (2005) 105(7):2658–63. doi:10.1182/blood-2004-09-3590

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

48. Ishii E, Ueda I, Shirakawa R, Yamamoto K, Horiuchi H, Ohga S, et al. Genetic subtypes of familial hemophagocytic lymphohistiocytosis: correlations with clinical features and cytotoxic T lymphocyte/natural killer cell functions. Blood (2005) 105(9):3442–8. doi:10.1182/blood-2004-08-3296

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

49. Katano H, Ali MA, Patera AC, Catalfamo M, Jaffe ES, Kimura H, et al. Chronic active Epstein-Barr virus infection associated with mutations in perforin that impair its maturation. Blood (2004) 103(4):1244–52. doi:10.1182/blood-2003-06-2171

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

50. Risma KA, Frayer RW, Filipovich AH, Sumegi J. Aberrant maturation of mutant perforin underlies the clinical diversity of hemophagocytic lymphohistiocytosis. J Clin Invest (2006) 116(1):182–92. doi:10.1172/JCI26217

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

51. Trambas C, Gallo F, Pende D, Marcenaro S, Moretta L, De Fusco C, et al. A single amino acid change, A91V, leads to conformational changes that can impair processing to the active form of perforin. Blood (2005) 106(3):932–7. doi:10.1182/blood-2004-09-3713

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

52. Voskoboinik I, Dunstone MA, Baran K, Whisstock JC, Trapani JA. Perforin: structure, function, and role in human immunopathology. Immunol Rev (2010) 235(1):35–54. doi:10.1111/j.0105-2896.2010.00896.x

CrossRef Full Text

53. Marcenaro S, Gallo F, Martini S, Santoro A, Griffiths GM, Arico M, et al. Analysis of natural killer-cell function in familial hemophagocytic lymphohistiocytosis (FHL): defective CD107a surface expression heralds Munc13-4 defect and discriminates between genetic subtypes of the disease. Blood (2006) 108(7):2316–23. doi:10.1182/blood-2006-04-015693

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

54. Bryceson YT, Rudd E, Zheng C, Edner J, Ma D, Wood SM, et al. Defective cytotoxic lymphocyte degranulation in syntaxin-11 deficient familial hemophagocytic lymphohistiocytosis 4 (FHL4) patients. Blood (2007) 110(6):1906–15. doi:10.1182/blood-2007-02-074468

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

55. Chia J, Thia K, Brennan AJ, Little M, Williams B, Lopez JA, et al. Fatal immune dysregulation due to a gain of glycosylation mutation in lymphocyte perforin. Blood (2012) 119(7):1713–6. doi:10.1182/blood-2011-08-374355

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

56. Clementi R, Chiocchetti A, Cappellano G, Cerutti E, Ferretti M, Orilieri E, et al. Variations of the perforin gene in patients with autoimmunity/lymphoproliferation and defective Fas function. Blood (2006) 108(9):3079–84. doi:10.1182/blood-2006-02-001412

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

57. Grom AA, Villanueva J, Lee S, Goldmuntz EA, Passo MH, Filipovich A. Natural killer cell dysfunction in patients with systemic-onset juvenile rheumatoid arthritis and macrophage activation syndrome. J Pediatr (2003) 142(3):292–6. doi:10.1067/mpd.2003.110

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

58. Molleran Lee S, Villanueva J, Sumegi J, Zhang K, Kogawa K, Davis J, et al. Characterisation of diverse PRF1 mutations leading to decreased natural killer cell activity in North American families with haemophagocytic lymphohistiocytosis. J Med Genet (2004) 41(2):137–44. doi:10.1136/jmg.2003.011528

CrossRef Full Text

59. Villanueva J, Lee S, Giannini EH, Graham TB, Passo MH, Filipovich A, et al. Natural killer cell dysfunction is a distinguishing feature of systemic onset juvenile rheumatoid arthritis and macrophage activation syndrome. Arthritis Res Ther (2005) 7(1):R30–7. doi:10.1186/ar1551

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

60. Voskoboinik I, Thia MC, De Bono A, Browne K, Cretney E, Jackson JT, et al. The functional basis for hemophagocytic lymphohistiocytosis in a patient with co-inherited missense mutations in the perforin (PFN1) gene. J Exp Med (2004) 200(6):811–6. doi:10.1084/jem.20040776

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

61. Voskoboinik I, Thia MC, Trapani JA. A functional analysis of the putative polymorphisms A91V and N252S and 22 missense perforin mutations associated with familial hemophagocytic lymphohistiocytosis. Blood (2005) 105(12):4700–6. doi:10.1182/blood-2004-12-4935

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

62. Hart TC, Hart PS, Bowden DW, Michalec MD, Callison SA, Walker SJ, et al. Mutations of the cathepsin C gene are responsible for Papillon-Lefevre syndrome. J Med Genet (1999) 36(12):881–7.

Pubmed Abstract | Pubmed Full Text

63. Hewitt C, McCormick D, Linden G, Turk D, Stern I, Wallace I, et al. The role of cathepsin C in Papillon-Lefevre syndrome, prepubertal periodontitis, and aggressive periodontitis. Hum Mutat (2004) 23(3):222–8. doi:10.1002/humu.10314

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

64. Toomes C, James J, Wood AJ, Wu CL, McCormick D, Lench N, et al. Loss-of-function mutations in the cathepsin C gene result in periodontal disease and palmoplantar keratosis. Nat Genet (1999) 23(4):421–4. doi:10.1038/70525

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

65. Pham CT, Ley TJ. Dipeptidyl peptidase I is required for the processing and activation of granzymes A and B in vivo. Proc Natl Acad Sci U S A (1999) 96(15):8627–32. doi:10.1073/pnas.96.15.8627

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

66. Pham CT, Ivanovich JL, Raptis SZ, Zehnbauer B, Ley TJ. Papillon-Lefevre syndrome: correlating the molecular, cellular, and clinical consequences of cathepsin C/dipeptidyl peptidase I deficiency in humans. J Immunol (2004) 173(12):7277–81.

Pubmed Abstract | Pubmed Full Text

67. Badolato R, Parolini S. Novel insights from adaptor protein 3 complex deficiency. J Allergy Clin Immunol (2007) 120(4):735–41; quiz 742–3. doi:10.1016/j.jaci.2007.08.039

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

68. Hermansky F, Cieslar P, Matousova O, Smetana K. Proceedings: study of albinism in relation to Hermansky-Pudlak syndrome. Thromb Diath Haemorrh (1975) 34(1):360.

69. Cullinane AR, Curry JA, Carmona-Rivera C, Summers CG, Ciccone C, Cardillo ND, et al. A BLOC-1 mutation screen reveals that PLDN is mutated in Hermansky-Pudlak syndrome type 9. Am J Hum Genet (2011) 88(6):778–87. doi:10.1016/j.ajhg.2011.05.009

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

70. Dell’Angelica EC. AP-3-dependent trafficking and disease: the first decade. Curr Opin Cell Biol (2009) 21(4):552–9. doi:10.1016/j.ceb.2009.04.014

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

71. Dell’Angelica EC, Shotelersuk V, Aguilar RC, Gahl WA, Bonifacino JS. Altered trafficking of lysosomal proteins in Hermansky-Pudlak syndrome due to mutations in the beta 3A subunit of the AP-3 adaptor. Mol Cell (1999) 3(1):11–21. doi:10.1016/S1097-2765(00)80170-7

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

72. Robinson MS, Bonifacino JS. Adaptor-related proteins. Curr Opin Cell Biol (2001) 13(4):444–53. doi:10.1016/S0955-0674(00)00235-0

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

73. Peden AA, Oorschot V, Hesser BA, Austin CD, Scheller RH, Klumperman J. Localization of the AP-3 adaptor complex defines a novel endosomal exit site for lysosomal membrane proteins. J Cell Biol (2004) 164(7):1065–76. doi:10.1083/jcb.200311064

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

74. Huizing M, Sarangarajan R, Strovel E, Zhao Y, Gahl WA, Boissy RE. AP-3 mediates tyrosinase but not TRP-1 trafficking in human melanocytes. Mol Biol Cell (2001) 12(7):2075–85. doi:10.1091/mbc.12.7.2075

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

75. Fontana S, Parolini S, Vermi W, Booth S, Gallo F, Donini M, et al. Innate immunity defects in Hermansky-Pudlak type 2 syndrome. Blood (2006) 107(12):4857–64. doi:10.1182/blood-2005-11-4398

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

76. Enders A, Zieger B, Schwarz K, Yoshimi A, Speckmann C, Knoepfle EM, et al. Lethal hemophagocytic lymphohistiocytosis in Hermansky-Pudlak syndrome type II. Blood (2006) 108(1):81–7. doi:10.1182/blood-2005-11-4413

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

77. Clark RH, Stinchcombe JC, Day A, Blott E, Booth S, Bossi G, et al. Adaptor protein 3-dependent microtubule-mediated movement of lytic granules to the immunological synapse. Nat Immunol (2003) 4(11):1111–20. doi:10.1038/ni1000

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

78. Olsen I, Bou-Gharios G, Abraham D. The activation of resting lymphocytes is accompanied by the biogenesis of lysosomal organelles. Eur J Immunol (1990) 20(10):2161–70. doi:10.1002/eji.1830201003

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

79. Isaaz S, Baetz K, Olsen K, Podack E, Griffiths GM. Serial killing by cytotoxic T lymphocytes: T cell receptor triggers degranulation, re-filling of the lytic granules and secretion of lytic proteins via a non-granule pathway. Eur J Immunol (1995) 25(4):1071–9. doi:10.1002/eji.1830250432

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

80. Bou-Gharios G, Moss J, Olsen I, Partridge T. Ultrastructural localization of a lysosomal enzyme in resin-embedded lymphocytes. Histochemistry (1988) 89(1):69–74. doi:10.1007/BF00496587

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

81. Dent PB, Fish LA, White LG, Good RA. Chediak-Higashi syndrome. Observations on the nature of the associated malignancy. Lab Invest (1966) 15(10):1634–42.

82. White JG. The Chediak-Higashi syndrome: a possible lysosomal disease. Blood (1966) 28(2):143–56.

83. Kaplan J, De Domenico I, Ward DM. Chediak-Higashi syndrome. Curr Opin Hematol (2008) 15(1):22–9. doi:10.1097/MOH.0b013e3282f2bcce

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

84. Barak Y, Nir E. Chediak-Higashi syndrome. Am J Pediatr Hematol Oncol (1987) 9(1):42–55. doi:10.1097/00043426-198721000-00008

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

85. Nagle DL, Karim MA, Woolf EA, Holmgren L, Bork P, Misumi DJ, et al. Identification and mutation analysis of the complete gene for Chediak-Higashi syndrome. Nat Genet (1996) 14(3):307–11. doi:10.1038/ng1196-307

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

86. Barbosa MD, Nguyen QA, Tchernev VT, Ashley JA, Detter JC, Blaydes SM, et al. Identification of the homologous beige and Chediak-Higashi syndrome genes. Nature (1996) 382(6588):262–5. doi:10.1038/382262a0

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

87. Ward DM, Griffiths GM, Stinchcombe JC, Kaplan J. Analysis of the lysosomal storage disease Chediak-Higashi syndrome. Traffic (2000) 1(11):816–22. doi:10.1034/j.1600-0854.2000.011102.x

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

88. Burkhardt JK, Wiebel FA, Hester S, Argon Y. The giant organelles in beige and Chediak-Higashi fibroblasts are derived from late endosomes and mature lysosomes. J Exp Med (1993) 178(6):1845–56. doi:10.1084/jem.178.6.1845

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

89. Roder JC, Haliotis T, Laing L, Kozbor D, Rubin P, Pross H, et al. Further studies of natural killer cell function in Chediak-Higashi patients. Immunology (1982) 46(3):555–60.

Pubmed Abstract | Pubmed Full Text

90. Roder JC, Haliotis T, Klein M, Korec S, Jett JR, Ortaldo J, et al. A new immunodeficiency disorder in humans involving NK cells. Nature (1980) 284(5756):553–5. doi:10.1038/284553a0

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

91. Klein M, Roder J, Haliotis T, Korec S, Jett JR, Herberman RB, et al. Chediak-Higashi gene in humans. II. The selectivity of the defect in natural-killer and antibody-dependent cell-mediated cytotoxicity function. J Exp Med (1980) 151(5):1049–58. doi:10.1084/jem.151.5.1049

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

92. Katz P, Zaytoun AM, Fauci AS. Deficiency of active natural killer cells in the Chediak-Higashi syndrome. Localization of the defect using a single cell cytotoxicity assay. J Clin Invest (1982) 69(6):1231–8. doi:10.1172/JCI110562

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

93. Haliotis T, Roder J, Klein M, Ortaldo J, Fauci AS, Herberman RB. Chediak-Higashi gene in humans I. Impairment of natural-killer function. J Exp Med (1980) 151(5):1039–48. doi:10.1084/jem.151.5.1039

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

94. Brahmi Z. Nature of natural killer cell hyporesponsiveness in the Chediak-Higashi syndrome. Hum Immunol (1983) 6(1):45–52. doi:10.1016/0198-8859(83)90072-1

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

95. Abo T, Roder JC, Abo W, Cooper MD, Balch CM. Natural killer (HNK-1+) cells in Chediak-Higashi patients are present in normal numbers but are abnormal in function and morphology. J Clin Invest (1982) 70(1):193–7. doi:10.1172/JCI110592

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

96. Targan SR, Oseas R. The “lazy” NK cells of Chediak-Higashi syndrome. J Immunol (1983) 130(6):2671–4.

Pubmed Abstract | Pubmed Full Text

97. Baetz K, Isaaz S, Griffiths GM. Loss of cytotoxic T lymphocyte function in Chediak-Higashi syndrome arises from a secretory defect that prevents lytic granule exocytosis. J Immunol (1995) 154(11):6122–31.

Pubmed Abstract | Pubmed Full Text

98. Stinchcombe JC, Page LJ, Griffiths GM. Secretory lysosome biogenesis in cytotoxic T lymphocytes from normal and Chediak Higashi syndrome patients. Traffic (2000) 1(5):435–44. doi:10.1034/j.1600-0854.2000.010508.x

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

99. Orange JS. Formation and function of the lytic NK-cell immunological synapse. Nat Rev Immunol (2008) 8(9):713–25. doi:10.1038/nri2381

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

100. Davis DM, Chiu I, Fassett M, Cohen GB, Mandelboim O, Strominger JL. The human natural killer cell immune synapse. Proc Natl Acad Sci U S A (1999) 96(26):15062–7. doi:10.1073/pnas.96.26.15062

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

101. Orange JS, Harris KE, Andzelm MM, Valter MM, Geha RS, Strominger JL. The mature activating natural killer cell immunologic synapse is formed in distinct stages. Proc Natl Acad Sci U S A (2003) 100(24):14151–6. doi:10.1073/pnas.1835830100

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

102. Vyas YM, Mehta KM, Morgan M, Maniar H, Butros L, Jung S, et al. Spatial organization of signal transduction molecules in the NK cell immune synapses during MHC class I-regulated noncytolytic and cytolytic interactions. J Immunol (2001) 167(8):4358–67.

Pubmed Abstract | Pubmed Full Text

103. Bryceson YT, Ljunggren HG, Long EO. Minimal requirement for induction of natural cytotoxicity and intersection of activation signals by inhibitory receptors. Blood (2009) 114(13):2657–66. doi:10.1182/blood-2009-01-201632

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

104. Bryceson YT, March ME, Barber DF, Ljunggren HG, Long EO. Cytolytic granule polarization and degranulation controlled by different receptors in resting NK cells. J Exp Med (2005) 202(7):1001–12. doi:10.1084/jem.20051143

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

105. Liu D, Bryceson YT, Meckel T, Vasiliver-Shamis G, Dustin ML, Long EO. Integrin-dependent organization and bidirectional vesicular traffic at cytotoxic immune synapses. Immunity (2009) 31(1):99–109. doi:10.1016/j.immuni.2009.05.009

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

106. Barber DF, Faure M, Long EO. LFA-1 contributes an early signal for NK cell cytotoxicity. J Immunol (2004) 173(6):3653–9.

Pubmed Abstract | Pubmed Full Text

107. Mentlik AN, Sanborn KB, Holzbaur EL, Orange JS. Rapid lytic granule convergence to the MTOC in natural killer cells is dependent on dynein but not cytolytic commitment. Mol Biol Cell (2010) 21(13):2241–56. doi:10.1091/mbc.E09-11-0930

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

108. Riteau B, Barber DF, Long EO. Vav1 phosphorylation is induced by beta2 integrin engagement on natural killer cells upstream of actin cytoskeleton and lipid raft reorganization. J Exp Med (2003) 198(3):469–74. doi:10.1084/jem.20021995

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

109. Kishimoto TK, Hollander N, Roberts TM, Anderson DC, Springer TA. Heterogeneous mutations in the beta subunit common to the LFA-1, Mac-1, and p150,95 glycoproteins cause leukocyte adhesion deficiency. Cell (1987) 50(2):193–202. doi:10.1016/0092-8674(87)90215-7

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

110. Hanna S, Etzioni A. Leukocyte adhesion deficiencies. Ann N Y Acad Sci (2012) 1250:50–5. doi:10.1111/j.1749-6632.2011.06389.x

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

111. Kohl S, Loo LS, Schmalstieg FS, Anderson DC. The genetic deficiency of leukocyte surface glycoprotein Mac-1, LFA-1, p150,95 in humans is associated with defective antibody-dependent cellular cytotoxicity in vitro and defective protection against herpes simplex virus infection in vivo. J Immunol (1986) 137(5):1688–94.

Pubmed Abstract | Pubmed Full Text

112. Kohl S, Springer TA, Schmalstieg FC, Loo LS, Anderson DC. Defective natural killer cytotoxicity and polymorphonuclear leukocyte antibody-dependent cellular cytotoxicity in patients with LFA-1/OKM-1 deficiency. J Immunol (1984) 133(6):2972–8.

Pubmed Abstract | Pubmed Full Text

113. Lau YL, Low LC, Jones BM, Lawton JW. Defective neutrophil and lymphocyte function in leucocyte adhesion deficiency. Clin Exp Immunol (1991) 85(2):202–8. doi:10.1111/j.1365-2249.1991.tb05705.x

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

114. James AM, Hsu HT, Dongre P, Uzel G, Mace EM, Banerjee PP, et al. Rapid activation receptor- or IL-2-induced lytic granule convergence in human natural killer cells requires Src, but not downstream signaling. Blood (2013) 121(14):2627–37. doi:10.1182/blood-2012-06-437012

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

115. Castriconi R, Dondero A, Cantoni C, Della Chiesa M, Prato C, Nanni M, et al. Functional characterization of natural killer cells in type I leukocyte adhesion deficiency. Blood (2007) 109(11):4873–81. doi:10.1182/blood-2006-08-038760

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

116. Moser M, Legate KR, Zent R, Fassler R. The tail of integrins, talin, and kindlins. Science (2009) 324(5929):895–9. doi:10.1126/science.1163865

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

117. Moser M, Nieswandt B, Ussar S, Pozgajova M, Fassler R. Kindlin-3 is essential for integrin activation and platelet aggregation. Nat Med (2008) 14(3):325–30. doi:10.1038/nm1722

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

118. Ye F, Petrich BG. Kindlin: helper, co-activator, or booster of talin in integrin activation? Curr Opin Hematol (2011) 18(5):356–60. doi:10.1097/MOH.0b013e3283497f09

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

119. Feigelson SW, Grabovsky V, Manevich-Mendelson E, Pasvolsky R, Shulman Z, Shinder V, et al. Kindlin-3 is required for the stabilization of TCR-stimulated LFA-1:ICAM-1 bonds critical for lymphocyte arrest and spreading on dendritic cells. Blood (2011) 117(26):7042–52. doi:10.1182/blood-2010-12-322859

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

120. Jurk K, Schulz AS, Kehrel BE, Rapple D, Schulze H, Mobest D, et al. Novel integrin-dependent platelet malfunction in siblings with leukocyte adhesion deficiency-III (LAD-III) caused by a point mutation in FERMT3. Thromb Haemost (2010) 103(5):1053–64. doi:10.1160/TH09-10-0689

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

121. Malinin NL, Zhang L, Choi J, Ciocea A, Razorenova O, Ma YQ, et al. A point mutation in KINDLIN3 ablates activation of three integrin subfamilies in humans. Nat Med (2009) 15(3):313–8. doi:10.1038/nm.1917

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

122. Manevich-Mendelson E, Feigelson SW, Pasvolsky R, Aker M, Grabovsky V, Shulman Z, et al. Loss of kindlin-3 in LAD-III eliminates LFA-1 but not VLA-4 adhesiveness developed under shear flow conditions. Blood (2009) 114(11):2344–53. doi:10.1182/blood-2009-04-218636

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

123. McDowall A, Svensson L, Stanley P, Patzak I, Chakravarty P, Howarth K, et al. Two mutations in the KINDLIN3 gene of a new leukocyte adhesion deficiency III patient reveal distinct effects on leukocyte function in vitro. Blood (2010) 115(23):4834–42. doi:10.1182/blood-2009-08-238709

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

124. Robert P, Canault M, Farnarier C, Nurden A, Grosdidier C, Barlogis V, et al. A novel leukocyte adhesion deficiency III variant: kindlin-3 deficiency results in integrin- and nonintegrin-related defects in different steps of leukocyte adhesion. J Immunol (2011) 186(9):5273–83. doi:10.4049/jimmunol.1003141

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

125. Svensson L, Howarth K, McDowall A, Patzak I, Evans R, Ussar S, et al. Leukocyte adhesion deficiency-III is caused by mutations in KINDLIN3 affecting integrin activation. Nat Med (2009) 15(3):306–12. doi:10.1038/nm.1931

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

126. Gruda R, Brown AC, Grabovsky V, Mizrahi S, Gur C, Feigelson SW, et al. Loss of kindlin-3 alters the threshold for NK cell activation in human leukocyte adhesion deficiency-III. Blood (2012) 120(19):3915–24. doi:10.1182/blood-2012-02-410795

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

127. Massaad MJ, Ramesh N, Geha RS. Wiskott-Aldrich syndrome: a comprehensive review. Ann N Y Acad Sci (2013) 1285:26–43. doi:10.1111/nyas.12049

CrossRef Full Text

128. Thrasher AJ, Burns SO. WASP: a key immunological multitasker. Nat Rev Immunol (2010) 10(3):182–92. doi:10.1038/nri2724

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

129. Parolini O, Berardelli S, Riedl E, Bello-Fernandez C, Strobl H, Majdic O, et al. Expression of Wiskott-Aldrich syndrome protein (WASP) gene during hematopoietic differentiation. Blood (1997) 90(1):70–5.

Pubmed Abstract | Pubmed Full Text

130. Stewart DM, Treiber-Held S, Kurman CC, Facchetti F, Notarangelo LD, Nelson DL. Studies of the expression of the Wiskott-Aldrich syndrome protein. J Clin Invest (1996) 97(11):2627–34. doi:10.1172/JCI118712

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

131. Derry JM, Ochs HD, Francke U. Isolation of a novel gene mutated in Wiskott-Aldrich syndrome. Cell (1994) 79(5):following922.

132. Orange JS, Stone KD, Turvey SE, Krzewski K. The Wiskott-Aldrich syndrome. Cell Mol Life Sci (2004) 61(18):2361–85. doi:10.1007/s00018-004-4086-z

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

133. Lim RP, Misra A, Wu Z, Thanabalu T. Analysis of conformational changes in WASP using a split YFP. Biochem Biophys Res Commun (2007) 362(4):1085–9. doi:10.1016/j.bbrc.2007.08.124

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

134. Hemsath L, Dvorsky R, Fiegen D, Carlier MF, Ahmadian MR. An electrostatic steering mechanism of Cdc42 recognition by Wiskott-Aldrich syndrome proteins. Mol Cell (2005) 20(2):313–24. doi:10.1016/j.molcel.2005.08.036

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

135. Higgs HN, Pollard TD. Activation by Cdc42 and PIP(2) of Wiskott-Aldrich syndrome protein (WASp) stimulates actin nucleation by Arp2/3 complex. J Cell Biol (2000) 150(6):1311–20. doi:10.1083/jcb.150.6.1311

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

136. Prehoda KE, Scott JA, Mullins RD, Lim WA. Integration of multiple signals through cooperative regulation of the N-WASP-Arp2/3 complex. Science (2000) 290(5492):801–6. doi:10.1126/science.290.5492.801

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

137. Rohatgi R, Ho HY, Kirschner MW. Mechanism of N-WASP activation by CDC42 and phosphatidylinositol 4, 5-bisphosphate. J Cell Biol (2000) 150(6):1299–310. doi:10.1083/jcb.150.6.1299

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

138. Symons M, Derry JM, Karlak B, Jiang S, Lemahieu V, McCormick F, et al. Wiskott-Aldrich syndrome protein, a novel effector for the GTPase CDC42Hs, is implicated in actin polymerization. Cell (1996) 84(5):723–34. doi:10.1016/S0092-8674(00)81050-8

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

139. Gismondi A, Cifaldi L, Mazza C, Giliani S, Parolini S, Morrone S, et al. Impaired natural and CD16-mediated NK cell cytotoxicity in patients with WAS and XLT: ability of IL-2 to correct NK cell functional defect. Blood (2004) 104(2):436–43. doi:10.1182/blood-2003-07-2621

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

140. Orange JS, Ramesh N, Remold-O’Donnell E, Sasahara Y, Koopman L, Byrne M, et al. Wiskott-Aldrich syndrome protein is required for NK cell cytotoxicity and colocalizes with actin to NK cell-activating immunologic synapses. Proc Natl Acad Sci U S A (2002) 99(17):11351–6. doi:10.1073/pnas.162376099

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

141. Orange JS, Roy-Ghanta S, Mace EM, Maru S, Rak GD, Sanborn KB, et al. IL-2 induces a WAVE2-dependent pathway for actin reorganization that enables WASp-independent human NK cell function. J Clin Invest (2011) 121(4):1535–48. doi:10.1172/JCI44862

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

142. Carlin LM, Evans R, Milewicz H, Fernandes L, Matthews DR, Perani M, et al. A targeted siRNA screen identifies regulators of Cdc42 activity at the natural killer cell immunological synapse. Sci Signal (2011) 4(201):ra81. doi:10.1126/scisignal.2001729

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

143. Sinai P, Nguyen C, Schatzle JD, Wulfing C. Transience in polarization of cytolytic effectors is required for efficient killing and controlled by Cdc42. Proc Natl Acad Sci U S A (2010) 107(26):11912–7. doi:10.1073/pnas.0913422107

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

144. Lanzi G, Moratto D, Vairo D, Masneri S, Delmonte O, Paganini T, et al. A novel primary human immunodeficiency due to deficiency in the WASP-interacting protein WIP. J Exp Med (2013) 209(1):29–34. doi:10.1084/jem.20110896

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

145. Garcia E, Jones GE, Machesky LM, Anton IM. WIP: WASP-interacting proteins at invadopodia and podosomes. Eur J Cell Biol (2012) 91(11–12):869–77. doi:10.1016/j.ejcb.2012.06.002

CrossRef Full Text

146. Anton IM, Jones GE, Wandosell F, Geha R, Ramesh N. WASP-interacting protein (WIP): working in polymerisation and much more. Trends Cell Biol (2007) 17(11):555–62. doi:10.1016/j.tcb.2007.08.005

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

147. Krzewski K, Chen X, Orange JS, Strominger JL. Formation of a WIP-, WASp-, actin-, and myosin IIA-containing multiprotein complex in activated NK cells and its alteration by KIR inhibitory signaling. J Cell Biol (2006) 173(1):121–32. doi:10.1083/jcb.200509076

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

148. Krzewski K, Chen X, Strominger JL. WIP is essential for lytic granule polarization and NK cell cytotoxicity. Proc Natl Acad Sci U S A (2008) 105(7):2568–73. doi:10.1073/pnas.0711593105

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

149. Cote JF, Vuori K. Identification of an evolutionarily conserved superfamily of DOCK180-related proteins with guanine nucleotide exchange activity. J Cell Sci (2002) 115(Pt 24):4901–13. doi:10.1242/jcs.00219

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

150. Cote JF, Vuori K. GEF what? Dock180 and related proteins help Rac to polarize cells in new ways. Trends Cell Biol (2007) 17(8):383–93. doi:10.1016/j.tcb.2007.05.001

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

151. Meller N, Merlot S, Guda C. CZH proteins: a new family of Rho-GEFs. J Cell Sci (2005) 118(Pt 21):4937–46. doi:10.1242/jcs.02671

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

152. Engelhardt KR, McGhee S, Winkler S, Sassi A, Woellner C, Lopez-Herrera G, et al. Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome. J Allergy Clin Immunol (2009) 124(6):1289–302.e4. doi:10.1016/j.jaci.2009.10.038

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

153. Zhang Q, Davis JC, Lamborn IT, Freeman AF, Jing H, Favreau AJ, et al. Combined immunodeficiency associated with DOCK8 mutations. N Engl J Med (2009) 361(21):2046–55. doi:10.1056/NEJMoa0905506

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

154. Su HC. Dedicator of cytokinesis 8 (DOCK8) deficiency. Curr Opin Allergy Clin Immunol (2010) 10(6):515–20. doi:10.1097/ACI.0b013e32833fd718

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

155. Ham H, Guerrier S, Kim J, Schoon RA, Anderson EL, Hamann MJ, et al. Dedicator of cytokinesis 8 interacts with talin and Wiskott-Aldrich syndrome protein to regulate NK cell cytotoxicity. J Immunol (2013) 190(7):3661–9. doi:10.4049/jimmunol.1202792

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

156. Mizesko MC, Banerjee PP, Monaco-Shawver L, Mace EM, Bernal WE, Sawalle-Belohradsky J, et al. Defective actin accumulation impairs human natural killer cell function in patients with dedicator of cytokinesis 8 deficiency. J Allergy Clin Immunol (2013) 131(3):840–8. doi:10.1016/j.jaci.2012.12.1568

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

157. Randall KL, Chan SS, Ma CS, Fung I, Mei Y, Yabas M, et al. DOCK8 deficiency impairs CD8 T cell survival and function in humans and mice. J Exp Med (2011) 208(11):2305–20. doi:10.1084/jem.20110345

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

158. Randall KL, Lambe T, Johnson AL, Treanor B, Kucharska E, Domaschenz H, et al. Dock8 mutations cripple B cell immunological synapses, germinal centers and long-lived antibody production. Nat Immunol (2009) 10(12):1283–91. doi:10.1038/ni.1820

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

159. Harada Y, Tanaka Y, Terasawa M, Pieczyk M, Habiro K, Katakai T, et al. DOCK8 is a Cdc42 activator critical for interstitial dendritic cell migration during immune responses. Blood (2012) 119(19):4451–61. doi:10.1182/blood-2012-01-407098

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

160. Di Paolo G, Pellegrini L, Letinic K, Cestra G, Zoncu R, Voronov S, et al. Recruitment and regulation of phosphatidylinositol phosphate kinase type 1 gamma by the FERM domain of talin. Nature (2002) 420(6911):85–9. doi:10.1038/nature01147

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

161. Ling K, Doughman RL, Firestone AJ, Bunce MW, Anderson RA. Type I gamma phosphatidylinositol phosphate kinase targets and regulates focal adhesions. Nature (2002) 420(6911):89–93. doi:10.1038/nature01082

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

162. Mace EM, Zhang J, Siminovitch KA, Takei F. Elucidation of the integrin LFA-1-mediated signaling pathway of actin polarization in natural killer cells. Blood (2010) 116(8):1272–9. doi:10.1182/blood-2009-12-261487

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

163. Cannon JL, Burkhardt JK. The regulation of actin remodeling during T-cell-APC conjugate formation. Immunol Rev (2002) 186:90–9. doi:10.1034/j.1600-065X.2002.18609.x

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

164. Eng EW, Bettio A, Ibrahim J, Harrison RE. MTOC reorientation occurs during FcgammaR-mediated phagocytosis in macrophages. Mol Biol Cell (2007) 18(7):2389–99. doi:10.1091/mbc.E06-12-1128

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

165. Etienne-Manneville S. Cdc42 – the centre of polarity. J Cell Sci (2004) 117(Pt 8):1291–300. doi:10.1242/jcs.01115

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

166. Pulecio J, Petrovic J, Prete F, Chiaruttini G, Lennon-Dumenil AM, Desdouets C, et al. Cdc42-mediated MTOC polarization in dendritic cells controls targeted delivery of cytokines at the immune synapse. J Exp Med (2010) 207(12):2719–32. doi:10.1084/jem.20100007

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

167. Stowers L, Yelon D, Berg LJ, Chant J. Regulation of the polarization of T cells toward antigen-presenting cells by Ras-related GTPase CDC42. Proc Natl Acad Sci U S A (1995) 92(11):5027–31. doi:10.1073/pnas.92.11.5027

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

168. Stinchcombe JC, Majorovits E, Bossi G, Fuller S, Griffiths GM. Centrosome polarization delivers secretory granules to the immunological synapse. Nature (2006) 443(7110):462–5. doi:10.1038/nature05071

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

169. Chen X, Trivedi PP, Ge B, Krzewski K, Strominger JL. Many NK cell receptors activate ERK2 and JNK1 to trigger microtubule organizing center and granule polarization and cytotoxicity. Proc Natl Acad Sci U S A (2007) 104(15):6329–34. doi:10.1073/pnas.0611655104

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

170. Graham DB, Cella M, Giurisato E, Fujikawa K, Miletic AV, Kloeppel T, et al. Vav1 controls DAP10-mediated natural cytotoxicity by regulating actin and microtubule dynamics. J Immunol (2006) 177(4):2349–55.

Pubmed Abstract | Pubmed Full Text

171. Sancho D, Nieto M, Llano M, Rodriguez-Fernandez JL, Tejedor R, Avraham S, et al. The tyrosine kinase PYK-2/RAFTK regulates natural killer (NK) cell cytotoxic response, and is translocated and activated upon specific target cell recognition and killing. J Cell Biol (2000) 149(6):1249–62. doi:10.1083/jcb.149.6.1249

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

172. Banerjee PP, Pandey R, Zheng R, Suhoski MM, Monaco-Shawver L, Orange JS. Cdc42-interacting protein-4 functionally links actin and microtubule networks at the cytolytic NK cell immunological synapse. J Exp Med (2007) 204(10):2305–20. doi:10.1084/jem.20061893

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

173. Kanwar N, Wilkins JA. IQGAP1 involvement in MTOC and granule polarization in NK-cell cytotoxicity. Eur J Immunol (2011) 41(9):2763–73. doi:10.1002/eji.201040444

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

174. Gorman JA, Babich A, Dick CJ, Schoon RA, Koenig A, Gomez TS, et al. The cytoskeletal adaptor protein IQGAP1 regulates TCR-mediated signaling and filamentous actin dynamics. J Immunol (2012) 188(12):6135–44. doi:10.4049/jimmunol.1103487

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

175. Sanchez-Ruiz J, Mejias R, Garcia-Belando M, Barber DF, Gonzalez-Garcia A. Ral GTPases regulate cell-mediated cytotoxicity in NK cells. J Immunol (2011) 187(5):2433–41. doi:10.4049/jimmunol.1003089

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

176. Tuli A, Thiery J, James AM, Michelet X, Sharma M, Garg S, et al. Arf-like GTPase Arl8b regulates lytic granule polarization and natural killer cell-mediated cytotoxicity. Mol Biol Cell (2013) 24(23):3721–35. doi:10.1091/mbc.E13-05-0259

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

177. Kurowska M, Goudin N, Nehme NT, Court M, Garin J, Fischer A, et al. Terminal transport of lytic granules to the immune synapse is mediated by the kinesin-1/Slp3/Rab27a complex. Blood (2012) 119(17):3879–89. doi:10.1182/blood-2011-09-382556

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

178. Stinchcombe JC, Salio M, Cerundolo V, Pende D, Arico M, Griffiths GM. Centriole polarisation to the immunological synapse directs secretion from cytolytic cells of both the innate and adaptive immune systems. BMC Biol (2011) 9:45. doi:10.1186/1741-7007-9-45

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

179. Brown AC, Oddos S, Dobbie IM, Alakoskela JM, Parton RM, Eissmann P, et al. Remodelling of cortical actin where lytic granules dock at natural killer cell immune synapses revealed by super-resolution microscopy. PLoS Biol (2011) 9(9):e1001152. doi:10.1371/journal.pbio.1001152

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

180. Rak GD, Mace EM, Banerjee PP, Svitkina T, Orange JS. Natural killer cell lytic granule secretion occurs through a pervasive actin network at the immune synapse. PLoS Biol (2011) 9(9):e1001151. doi:10.1371/journal.pbio.1001151

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

181. Heissler SM, Manstein DJ. Nonmuscle myosin-2: mix and match. Cell Mol Life Sci (2013) 70(1):1–21. doi:10.1007/s00018-012-1002-9

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

182. Eddinger TJ, Meer DP. Myosin II isoforms in smooth muscle: heterogeneity and function. Am J Physiol Cell Physiol (2007) 293(2):C493–508. doi:10.1152/ajpcell.00131.2007

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

183. Ricketson D, Johnston CA, Prehoda KE. Multiple tail domain interactions stabilize nonmuscle myosin II bipolar filaments. Proc Natl Acad Sci U S A (2010) 107(49):20964–9. doi:10.1073/pnas.1007025107

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

184. Sellers JR. Myosins: a diverse superfamily. Biochim Biophys Acta (2000) 1496(1):3–22. doi:10.1016/S0167-4889(00)00005-7

CrossRef Full Text

185. Even-Ram S, Yamada KM. Of mice and men: relevance of cellular and molecular characterizations of myosin IIA to MYH9-related human disease. Cell Adh Migr (2007) 1(3):152–5. doi:10.4161/cam.1.3.5089

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

186. Seri M, Pecci A, Di Bari F, Cusano R, Savino M, Panza E, et al. MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single illness. Medicine (Baltimore) (2003) 82(3):203–15. doi:10.1097/01.md.0000076006.64510.5c

CrossRef Full Text

187. Ito M, Tanabe F, Sato A, Ishida E, Takami Y, Shigeta S. Inhibition of natural killer cell-mediated cytotoxicity by ML-9, a selective inhibitor of myosin light chain kinase. Int J Immunopharmacol (1989) 11(2):185–90. doi:10.1016/0192-0561(89)90070-2

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

188. Andzelm MM, Chen X, Krzewski K, Orange JS, Strominger JL. Myosin IIA is required for cytolytic granule exocytosis in human NK cells. J Exp Med (2007) 204(10):2285–91. doi:10.1084/jem.20071143

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

189. Sanborn KB, Mace EM, Rak GD, Difeo A, Martignetti JA, Pecci A, et al. Phosphorylation of the myosin IIA tailpiece regulates single myosin IIA molecule association with lytic granules to promote NK-cell cytotoxicity. Blood (2011) 118(22):5862–71. doi:10.1182/blood-2011-03-344846

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

190. Sanborn KB, Rak GD, Maru SY, Demers K, Difeo A, Martignetti JA, et al. Myosin IIA associates with NK cell lytic granules to enable their interaction with F-actin and function at the immunological synapse. J Immunol (2009) 182(11):6969–84. doi:10.4049/jimmunol.0804337

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

191. Liu D, Meckel T, Long EO. Distinct role of rab27a in granule movement at the plasma membrane and in the cytosol of NK cells. PLoS One (2010) 5(9):e12870. doi:10.1371/journal.pone.0012870

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

192. Wood SM, Meeths M, Chiang SC, Bechensteen AG, Boelens JJ, Heilmann C, et al. Different NK cell-activating receptors preferentially recruit Rab27a or Munc13-4 to perforin-containing granules for cytotoxicity. Blood (2009) 114(19):4117–27. doi:10.1182/blood-2009-06-225359

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

193. Lee MT, Mishra A, Lambright DG. Structural mechanisms for regulation of membrane traffic by rab GTPases. Traffic (2009) 10(10):1377–89. doi:10.1111/j.1600-0854.2009.00942.x

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

194. Pfeffer S, Aivazian D. Targeting Rab GTPases to distinct membrane compartments. Nat Rev Mol Cell Biol (2004) 5(11):886–96. doi:10.1038/nrm1500

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

195. Menasche G, Pastural E, Feldmann J, Certain S, Ersoy F, Dupuis S, et al. Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome. Nat Genet (2000) 25(2):173–6. doi:10.1038/76024

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

196. Sanal O, Ersoy F, Tezcan I, Metin A, Yel L, Menasche G, et al. Griscelli disease: genotype-phenotype correlation in an array of clinical heterogeneity. J Clin Immunol (2002) 22(4):237–43. doi:10.1023/A:1016045026204

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

197. Jahn R, Scheller RH. SNAREs – engines for membrane fusion. Nat Rev Mol Cell Biol (2006) 7(9):631–43. doi:10.1038/nrm2002

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

198. Stow JL, Manderson AP, Murray RZ. SNAREing immunity: the role of SNAREs in the immune system. Nat Rev Immunol (2006) 6(12):919–29. doi:10.1038/nri1980

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

199. Sudhof TC, Rothman JE. Membrane fusion: grappling with SNARE and SM proteins. Science (2009) 323(5913):474–7. doi:10.1126/science.1161748

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

200. Rudd E, Goransdotter Ericson K, Zheng C, Uysal Z, Ozkan A, Gurgey A, et al. Spectrum and clinical implications of syntaxin 11 gene mutations in familial haemophagocytic lymphohistiocytosis: association with disease-free remissions and haematopoietic malignancies. J Med Genet (2006) 43(4):e14. doi:10.1136/jmg.2005.035253

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

201. zur Stadt U, Schmidt S, Kasper B, Beutel K, Diler AS, Henter JI, et al. Linkage of familial hemophagocytic lymphohistiocytosis (FHL) type-4 to chromosome 6q24 and identification of mutations in syntaxin 11. Hum Mol Genet (2005) 14(6):827–34. doi:10.1093/hmg/ddi076

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

202. Jahn R, Fasshauer D. Molecular machines governing exocytosis of synaptic vesicles. Nature (2012) 490(7419):201–7. doi:10.1038/nature11320

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

203. Cote M, Menager MM, Burgess A, Mahlaoui N, Picard C, Schaffner C, et al. Munc18-2 deficiency causes familial hemophagocytic lymphohistiocytosis type 5 and impairs cytotoxic granule exocytosis in patient NK cells. J Clin Invest (2009) 119(12):3765–73. doi:10.1172/JCI40732

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

204. Feldmann J, Callebaut I, Raposo G, Certain S, Bacq D, Dumont C, et al. Munc13-4 is essential for cytolytic granules fusion and is mutated in a form of familial hemophagocytic lymphohistiocytosis (FHL3). Cell (2003) 115(4):461–73. doi:10.1016/S0092-8674(03)00855-9

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

205. zur Stadt U, Rohr J, Seifert W, Koch F, Grieve S, Pagel J, et al. Familial hemophagocytic lymphohistiocytosis type 5 (FHL-5) is caused by mutations in Munc18-2 and impaired binding to syntaxin 11. Am J Hum Genet (2009) 85(4):482–92. doi:10.1016/j.ajhg.2009.09.005

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

206. Maul-Pavicic A, Chiang SC, Rensing-Ehl A, Jessen B, Fauriat C, Wood SM, et al. ORAI1-mediated calcium influx is required for human cytotoxic lymphocyte degranulation and target cell lysis. Proc Natl Acad Sci U S A (2011) 108(8):3324–9. doi:10.1073/pnas.1013285108

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

207. Feske S, Picard C, Fischer A. Immunodeficiency due to mutations in ORAI1 and STIM1. Clin Immunol (2010) 135(2):169–82. doi:10.1016/j.clim.2010.01.011

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

208. Fukuda M. Versatile role of Rab27 in membrane trafficking: focus on the Rab27 effector families. J Biochem (2005) 137(1):9–16. doi:10.1093/jb/mvi002

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

209. Griscelli C, Durandy A, Guy-Grand D, Daguillard F, Herzog C, Prunieras M. A syndrome associating partial albinism and immunodeficiency. Am J Med (1978) 65(4):691–702. doi:10.1016/0002-9343(78)90858-6

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

210. Meeths M, Bryceson YT, Rudd E, Zheng C, Wood SM, Ramme K, et al. Clinical presentation of Griscelli syndrome type 2 and spectrum of RAB27A mutations. Pediatr Blood Cancer (2010) 54(4):563–72. doi:10.1002/pbc.22357

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

211. Menasche G, Ho CH, Sanal O, Feldmann J, Tezcan I, Ersoy F, et al. Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1). J Clin Invest (2003) 112(3):450–6. doi:10.1172/JCI200318264

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

212. Strom M, Hume AN, Tarafder AK, Barkagianni E, Seabra MC. A family of Rab27-binding proteins. Melanophilin links Rab27a and myosin Va function in melanosome transport. J Biol Chem (2002) 277(28):25423–30. doi:10.1074/jbc.M202574200

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

213. Hume AN, Collinson LM, Hopkins CR, Strom M, Barral DC, Bossi G, et al. The leaden gene product is required with Rab27a to recruit myosin Va to melanosomes in melanocytes. Traffic (2002) 3(3):193–202. doi:10.1034/j.1600-0854.2002.030305.x

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

214. Gazit R, Aker M, Elboim M, Achdout H, Katz G, Wolf DG, et al. NK cytotoxicity mediated by CD16 but not by NKp30 is functional in Griscelli syndrome. Blood (2007) 109(10):4306–12. doi:10.1182/blood-2006-09-047159

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

215. Klein C, Philippe N, Le Deist F, Fraitag S, Prost C, Durandy A, et al. Partial albinism with immunodeficiency (Griscelli syndrome). J Pediatr (1994) 125(6 Pt 1):886–95. doi:10.1016/S0022-3476(05)82003-7

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

216. Mancini AJ, Chan LS, Paller AS. Partial albinism with immunodeficiency: Griscelli syndrome: report of a case and review of the literature. J Am Acad Dermatol (1998) 38(2 Pt 2):295–300. doi:10.1016/S0190-9622(98)70568-7

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

217. Plebani A, Ciravegna B, Ponte M, Mingari MC, Moretta L. Interleukin-2 mediated restoration of natural killer cell function in a patient with Griscelli syndrome. Eur J Pediatr (2000) 159(9):713–4. doi:10.1007/s004310000501

CrossRef Full Text

218. Haddad EK, Wu X, Hammer JA III, Henkart PA. Defective granule exocytosis in Rab27a-deficient lymphocytes from Ashen mice. J Cell Biol (2001) 152(4):835–42. doi:10.1083/jcb.152.4.835

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

219. Stinchcombe JC, Barral DC, Mules EH, Booth S, Hume AN, Machesky LM, et al. Rab27a is required for regulated secretion in cytotoxic T lymphocytes. J Cell Biol (2001) 152(4):825–34. doi:10.1083/jcb.152.4.825

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

220. Holt O, Kanno E, Bossi G, Booth S, Daniele T, Santoro A, et al. Slp1 and Slp2-a localize to the plasma membrane of CTL and contribute to secretion from the immunological synapse. Traffic (2008) 9(4):446–57. doi:10.1111/j.1600-0854.2008.00714.x

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

221. Menasche G, Menager MM, Lefebvre JM, Deutsch E, Athman R, Lambert N, et al. A newly identified isoform of Slp2a associates with Rab27a in cytotoxic T cells and participates to cytotoxic granule secretion. Blood (2008) 112(13):5052–62. doi:10.1182/blood-2008-02-141069

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

222. Menager MM, Menasche G, Romao M, Knapnougel P, Ho CH, Garfa M, et al. Secretory cytotoxic granule maturation and exocytosis require the effector protein hMunc13-4. Nat Immunol (2007) 8(3):257–67. doi:10.1038/ni1431

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

223. Katano H, Cohen JI. Perforin and lymphohistiocytic proliferative disorders. Br J Haematol (2005) 128(6):739–50. doi:10.1111/j.1365-2141.2004.05305.x

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

224. Rohr J, Beutel K, Maul-Pavicic A, Vraetz T, Thiel J, Warnatz K, et al. Atypical familial hemophagocytic lymphohistiocytosis due to mutations in UNC13D and STXBP2 overlaps with primary immunodeficiency diseases. Haematologica (2010) 95(12):2080–7. doi:10.3324/haematol.2010.029389

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

225. Santoro A, Cannella S, Bossi G, Gallo F, Trizzino A, Pende D, et al. Novel Munc13-4 mutations in children and young adult patients with haemophagocytic lymphohistiocytosis. J Med Genet (2006) 43(12):953–60. doi:10.1136/jmg.2006.041863

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

226. Neeft M, Wieffer M, de Jong AS, Negroiu G, Metz CH, van Loon A, et al. Munc13-4 is an effector of rab27a and controls secretion of lysosomes in hematopoietic cells. Mol Biol Cell (2005) 16(2):731–41. doi:10.1091/mbc.E04-10-0923

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

227. Shirakawa R, Higashi T, Tabuchi A, Yoshioka A, Nishioka H, Fukuda M, et al. Munc13-4 is a GTP-Rab27-binding protein regulating dense core granule secretion in platelets. J Biol Chem (2004) 279(11):10730–7. doi:10.1074/jbc.M309426200

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

228. Tang BL, Low DY, Hong W. Syntaxin 11: a member of the syntaxin family without a carboxyl terminal transmembrane domain. Biochem Biophys Res Commun (1998) 245(2):627–32. doi:10.1006/bbrc.1998.8490

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

229. Prekeris R, Klumperman J, Scheller RH. Syntaxin 11 is an atypical SNARE abundant in the immune system. Eur J Cell Biol (2000) 79(11):771–80. doi:10.1078/0171-9335-00109

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

230. Arneson LN, Brickshawana A, Segovis CM, Schoon RA, Dick CJ, Leibson PJ. Cutting edge: syntaxin 11 regulates lymphocyte-mediated secretion and cytotoxicity. J Immunol (2007) 179(6):3397–401.

Pubmed Abstract | Pubmed Full Text

231. D’Orlando O, Zhao F, Kasper B, Orinska Z, Muller J, Hermans-Borgmeyer I, et al. Syntaxin 11 is required for NK and CD8(+) T-cell cytotoxicity and neutrophil degranulation. Eur J Immunol (2013) 43(1):194–208. doi:10.1002/eji.201142343

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

232. Kogl T, Muller J, Jessen B, Schmitt-Graeff A, Janka G, Ehl S, et al. Hemophagocytic lymphohistiocytosis in syntaxin-11-deficient mice: T-cell exhaustion limits fatal disease. Blood (2013) 121(4):604–13. doi:10.1182/blood-2012-07-441139

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

233. Dabrazhynetskaya A, Ma J, Guerreiro-Cacais AO, Arany Z, Rudd E, Henter JI, et al. Syntaxin 11 marks a distinct intracellular compartment recruited to the immunological synapse of NK cells to colocalize with cytotoxic granules. J Cell Mol Med (2012) 16(1):129–41. doi:10.1111/j.1582-4934.2011.01280.x

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

234. Valdez AC, Cabaniols JP, Brown MJ, Roche PA. Syntaxin 11 is associated with SNAP-23 on late endosomes and the trans-Golgi network. J Cell Sci (1999) 112(Pt 6):845–54.

Pubmed Abstract | Pubmed Full Text

235. Krzewski K, Gil-Krzewska A, Watts J, Stern JN, Strominger JL. VAMP4- and VAMP7-expressing vesicles are both required for cytotoxic granule exocytosis in NK cells. Eur J Immunol (2011) 41(11):3323–9. doi:10.1002/eji.201141582

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

236. Marcet-Palacios M, Odemuyiwa SO, Coughlin JJ, Garofoli D, Ewen C, Davidson CE, et al. Vesicle-associated membrane protein 7 (VAMP-7) is essential for target cell killing in a natural killer cell line. Biochem Biophys Res Commun (2008) 366(3):617–23. doi:10.1016/j.bbrc.2007.11.079

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

237. Meeths M, Entesarian M, Al-Herz W, Chiang SC, Wood SM, Al-Ateeqi W, et al. Spectrum of clinical presentations in familial hemophagocytic lymphohistiocytosis type 5 patients with mutations in STXBP2. Blood (2010) 116(15):2635–43. doi:10.1182/blood-2010-05-282541

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Keywords: NK cells, primary immunodeficiency, NK cell cytotoxicity, cytotoxic lymphocytes, cytotoxic synapse, lytic granules

Citation: Ham H and Billadeau DD (2014) Human immunodeficiency syndromes affecting human natural killer cell cytolytic activity. Front. Immunol. 5:2. doi: 10.3389/fimmu.2014.00002

Received: 05 November 2013; Paper pending published: 02 December 2013;
Accepted: 03 January 2014; Published online: 21 January 2014.

Edited by:

Konrad Krzewski, National Institutes of Health, USA

Reviewed by:

Jordan Orange, Baylor College of Medicine, USA
Björn Önfelt, Karolinska Institutet, Sweden

Copyright: © 2014 Ham and Billadeau. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Daniel D. Billadeau, Division of Oncology Research and Schulze Center for Novel Therapeutics, College of Medicine, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA e-mail: billadeau.daniel@mayo.edu

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