Xiaorui Song1
Lingling Wang
Linsheng Song- 1Liaoning Key Laboratory of Marine Animal Immunology, Dalian Ocean University, Dalian, China
- 2Laboratory for Marine Fisheries Science and Food Production Processes, Qingdao National Laboratory for Marine Science and Technology, Qingdao, China
- 3Liaoning Key Laboratory of Marine Animal Immunology and Disease Control, Dalian Ocean University, Dalian, China
Biomineralization refers to the dynamic physiological processes whereby living organisms elaborate mineralized tissues. The existence of extremely abundant molluscan species shows the diversity of mineralized tissues, since the majority of them (Conchifera) produce shells that vary in size and shape. Over the past decades, great progress has been made on the study of the cellular biology of shell biomineralization. The construction of the molluscan shell is the archetype of biologically controlled mineralization which requires specialized cellular machinery. It has been so far demonstrated that the cells involved in shell formation come from two different sources: outer mantle epithelial cells (OME) and circulating hemocytes. OMEs secrete the organic matrix, among which shell matrix proteins (SMPs) determine mineralogical and crystallographic properties of shell. Circulating hemocytes take part in the deposition of intracellular biominerals and deliver them to the mineralization sites. Many novel SMPs have been identified by using molecular biology techniques (i.e., gene cloning, in situ hybridization, immunohistochemistry) coupled with high-throughput sequencing data (genome, proteome, secretome and transcriptome), and their corresponding functions during the shell formation have also been confirmed. The cellular activity of OME and hemocytes during shell formation are significantly increased during shell regeneration process. A potential cellular basis model for molluscan shell formation is proposed. The shell matrix proteins, mostly secreted from OME, and a few secreted from hemocytes or other organs, are either directly delivered to the mineralization site via exosome or classical secretory pathway, or first transported to the hemolymph, and then engulfed by hemocytes (mainly granulocytes), which will disintegrate and release shell proteins and CaCO3 crystals at the mineralization front. OME and hemocytes may also be involved in the nucleation and remodeling process of CaCO3 mineral. These cells and cell products work co-operatively to produce an organo-mineral shell, which is composed of various biomineral ultra-structures and macromolecular organic components.
Introduction
Biomineralization refers to an extraordinary dynamic biological process whereby a living organism produces biomineral structures (a rigid skeleton or a non-skeletal mineral) at ambient temperature in environments ranging from polar to tropical (Simkiss and Wilbur, 1989; Cusack and Freer, 2008; Shi et al., 2013; Tang et al., 2018). Biomineral structures are of wide existence in nature with polymorphism and multiple functions. So far, at least 60 different biominerals have been identified to play versatile functions, including tissues support, embryonic and UV protection, shelter against predation, nutrition, reproduction, gravity, light or magnetic field perceptions, storage of mineral ions (Cusack and Freer, 2008; Marin et al., 2008; Islam and Peng, 2018). In the metazoan world, CaCO3 skeletons are the most abundant and most commonly encountered biominerals (Lowenstam and Weiner, 1989; Simkiss and Wilbur, 1989; Marin et al., 2007; Cusack and Freer, 2008; Marin et al., 2008). The phylum Mollusca is the second largest invertebrate phylum, which benefits from the protection from their external biomineralized structure, the shell, a kind of the mastery of cellular-engineered microstructures (Kocot et al., 2016).
Molluscan separate the biomineral formation from the ambient environment (Rahman and Shinjo, 2012) and exhibit a huge diversity of biomineral morphologies, such as shells from most molluscs, epithelial spicules of the basal mollusk Wirenia argentea (Solenogastres) (Todt and Wanninger, 2010), scales and plates in bivalves, operculum in gastropod Rapana venosa (Hashimoto et al., 2012), intracellular detoxifying granules in the common garden snail Helix aspersa (Howard et al., 1981), egg capsules of the Patagonian neogastropod Odontocymbiola magellanica (Bigatti et al., 2010), love dart of land snails (Lodi and Koene, 2016), pearls from pearl oyster, statoconia in Aplysia californica (Kondrachuk and Wiederhold, 2004), and statoliths in Nassarius reticulatus (Caenogastropoda) (Galante-Oliveira et al., 2014). The shell is the most well-known CaCO3 biominerals in molluscan animals, which contributes to support and protect them from predators, pathogens and to some extent from other environmental conditions, such as desiccation, wave action and iceberg damage (Kouchinsky, 2000; Cusack and Freer, 2008). Molluscs utilize a highly cross-linked protein layer (periostracum) and the outer mantle epithelial cells (OME), between where they elaborate a matrix comprising various macromolecules serving as the framework (Wilbur and Saleuddin, 1983; Lowenstam and Weiner, 1989; Addadi et al., 2006). Generally, the molluscan shell is made of approximately 95% CaCO3 and 1–5% organic matrix. CaCO3 exists as different crystal polymorphs (i.e., calcite, aragonite, vaterite) under natural conditions, and is arranged in layers with a distinctive pattern to form complex biomineral microstructures in molluscan shells. So far, more than 30 different biomineral microstructures of mollusc CaCO3, such as nacre, foliate, prismatic, cross lamellar, and homogeneous microstructure, have been documented based on the scanning electron microscopy (SEM) observations (Chateigner et al., 2000; Kouchinsky, 2000; Furuhashi et al., 2009).
A typical molluscan shell (i.e., the shells of the mussel, the oyster, the abalone and the nautilus) exhibits a trilayered structure: the outermost layer periostracum (a thin organic leathery layer), and two calcified layers (the outer prismatic layer and the inner nacreous layer) (Saruwatari et al., 2009). The prismatic layer is composed of elongated calcitic crystals in the form of prisms perpendicular to the periostracum. The nacreous layer, namely the inner lustrous shell layer, is composed of laminar structure made up of aragonite crystals, organized in a brick wall-like structure (Marie et al., 2012). Because of its extremely high fracture-resistance properties, nacre is considered as the most fascinating mollusk shell microstructures (Marin et al., 2012). As mentioned above, molluscan shell is a composite of inorganic mineral (mainly CaCO3) and organic matrix, which is secreted from the mantle epithelium, and comprised of proteins, peptides, lipids, and carbohydrates (Lowenstam and Weiner, 1989; Addadi et al., 2006). The cooperation mechanism of these disparate components in producing a highly structured biomineralized shell has not been fully understood despite decades of investigations. Scientists have traditionally recognized the matrix-mediated hypothesis, which states that the organic matrix exclusively control the molluscan shell formation by providing the framework, inducing crystal nucleation, and regulating crystal growth extracellularly, thereby forming the crystal morphologies that are unique to the various layers of molluscan shell (Addadi et al., 1987, 2006; Lowenstam and Weiner, 1989). However, these results were mostly revealed from in vitro experiments through mimicking internal microenvironment, thus the effect of matrix proteins on shell mineralization is questionable (Sikes et al., 2000; Mount et al., 2004). One alternative to the matrix-mediated hypothesis is the cell-mediated hypothesis, which proposes that crystal nucleation occurs in hemocytes or OME, and that crystal-bearing cells transport nascent crystals intracellularly to the mineralization front (Mount et al., 2004; Gong et al., 2008a; Xiang et al., 2014). Although the cellular basis has been reported in many other biomineralization, such as osteoclasts and primary mesenchyme cells involved in bone and spicule formation in vertebrates and echinoderms, respectively (Wilt, 2002; Kylmaoja et al., 2016), this hypothesis still largely scraps the dominant paradigm in molluscan biomineralization, and has been supported by increasing evidence, which will be introduced in the following text (Mount et al., 2004; Fleury et al., 2008; Johnstone et al., 2008, 2015; Cho and Jeong, 2011; Kong et al., 2015; Li et al., 2016). To date, cells coming from two different sources have been observed involved in shell formation: (1) OMEs mediate shell formation by either directly involving in the nucleation and remodeling process of CaCO3 mineral (Kong et al., 2015) or secreting the organic matrix, among which shell matrix proteins (SMPs) regulate the diversity of shell shapes by orchestrating the CaCO3 crystals in a specific manner (Lowenstam and Weiner, 1989; Zhang and Zhang, 2006; Marin et al., 2008; Ivanina et al., 2017); and (2) hemocytes participate in the deposition of intracellular CaCO3 crystals and deliver them to the mineralization site (Mount et al., 2004; Fleury et al., 2008; Kádár, 2008; Mount and Pickering, 2009; Cho and Jeong, 2011; Johnstone et al., 2015; Li et al., 2016; Ivanina et al., 2017). In this review, we give a brief description of the OME- and hemocyte-mediated cellular biomineralization of marine molluscs.
OME-Mediated Shell Mineralization in Molluscs
The mantle tissue can be divided into several specialized regions (inner epithelium, internal tissues, and outer epithelium) from inside to outside (Figure 1). The outer epithelium is known to be related to the shell formation process, owing to its proximity to the mineralization front (Nudelman et al., 2006). The OMEs on the surface of outer epithelium further comprise a subtle cell zonation (mantle edge and mantle pallial), and appears to be strictly associated with the different microstructures of shell formation (Marin et al., 2008). Generally, SMPs secreted from the mantle edge cells are involved in the prismatic layer formation, while SMPs produced from mantle pallial cells participate in nacreous layer formation (Miyamoto et al., 1996). This zonation has been evidenced in molluscs by in situ hybridization or immunohistology techniques. For example, the localization of Pif 80 was checked by means of immunohistochemical SEM image analysis, and positive immunosignals could be observed throughout the nacreous layer after incubation with the antibody to Pif 80 (Suzuki et al., 2009). Shell organic constitutes synthesized by OME can be generally classified into two categories: insoluble (mostly chitin and silk) and soluble proteins. The insoluble proteins often act as a framework for shell formation and involves in the strengthening of shell mechanical properties, while the soluble ones are essential factors determining mineralogical and crystallographic properties (Addadi et al., 2006; Morse et al., 2007; Cusack and Freer, 2008; Marin et al., 2008; Marie et al., 2012). For example, some molecules function as Ca2+ chelators, mineral nucleators or inhibitors (Nudelman et al., 2006; Yan et al., 2007), some regulate crystal shape (Albeck et al., 1993), and some determine which CaCO3 polymorph will form (Falini et al., 1996; Fu et al., 2005; Marie et al., 2012). This section summarizes the SMPs identified so far from the shells of molluscs, and emphasizes the physiological function of several critical SMPs through biochemical and micromorphological studies during shell biosynthesis.
Figure 1. Schematic presentation of shell biomineralization in the oyster (Wang et al., 2013a; Kong et al., 2015; Li et al., 2016). The notes for some of the shapes included in this figure are shown on the upper left. In general, the figure is divided into two parts: soft body and shell. Crystal-bearing hemocytes in the circulating system of oyster are released into the EPF by secretory cavities on the mantle surface and then transported to the biomineralization front. These hemocytes fuse into the prismatic layer columns. They release CaCO3 crystals to form the calcite of the prismatic layers. The fragmented hemocytes assist organic matrices secreted from OMEs to produce the substrate of the prismatic layer. Some shell proteins produced by organs other than the mantle (i.e., the shell proteins not produced by the mantle) may arrive into the hemocoel first and then be engulfed by the granulocytes. The hemocytes and OMEs might be directly involved in the shell regeneration by affixing on the shell regeneration area.
The Molecular Characteristic of SMPs
Shell matrix proteins are crucial factors for biomineralization processes, and the evolution of SMPs can reflect the diversification characters of molluscan shell (Marin et al., 2008; Marie et al., 2012). Traditionally, SMPs were retrieved from the soluble or insoluble organic fractions after dissolving the shell powder into calcium-chelating agents (i.e., EDTA or weak acid) (Marin et al., 2008). The soluble organic fractions were usually enriched in acidic hydrophilic residues (i.e., Asp), while the insoluble fraction contained a high ratio of Gly and Ala (Lowenstam and Weiner, 1989). With the widespread use of molecular biology techniques, more transcripts encoding SMPs were identified (Miyashita et al., 2000; Zhang et al., 2003). In recent years, the mollusc genome project has made great progress (Zhang et al., 2012; Du et al., 2017). Increases the sequence data of SMPs combined with transcriptome and proteome of molluscan mantle and shell have enabled a more thorough investigation into the biomineralization process (Zhang and Zhang, 2006; Politi et al., 2007; Cusack and Freer, 2008; Marin et al., 2008; Furuhashi et al., 2009; Kadar et al., 2009; Marie et al., 2010). For example, the mantle edge of Mytilus galloprovincialis was divided into three regions, and large amounts of differentially abundant transcripts across the three mantle regions were revealed (Bjärnmark et al., 2016). The highly polymorphic genome of the pearl oyster Pinctada fucata martensii, together with transcriptomic and proteomic analyses, allowed the identification of many SMPs (Du et al., 2017). So far, more than 60 different SMPs have been reported (Table 1). In this section, we will discuss the identification and evolution of functional SMPs from the prismatic and nacreous layers of molluscan shells as well as from extrapallial fluid (EPF), and the function of some critical SMPs is highlighted.
Table 1. The main shell matrix proteins identified from Molluscs.
SMPs in the Nacreous Layer
The nacreous layer has attracted most attention for its unique material properties and hierarchical order as well as contribution to the pearl agriculture industry (Jackson et al., 1988; Chateigner et al., 2000; Kono et al., 2000). According to transmission electron microscope (TEM)/SEM observations and X-Ray diffraction (XRD) measurements, the nacreous layer is mainly constituted of aragonite tablets (Marie et al., 2015, 2017). A large number of SMPs involved in the nacreous layer formation have been identified, such as Pif (Suzuki et al., 2009), MSI60 (Sudo et al., 1997), lustrin A (Shen et al., 1997), N16/pearlin (Samata et al., 1999; Miyashita et al., 2000), perlucin, perlustrin (Weiss et al., 2000), N14, N66 (Kono et al., 2000), mucoperlin (Marin et al., 2000), AP7, AP24 (Michenfelder et al., 2003), P10 (Zhang et al., 2006a), perlwapin (Treccani et al., 2006), perlinhibin (Mann et al., 2007), N19 (Yano et al., 2007), N40 (Yan et al., 2007) and blue mussel shell protein (BMSP) (Suzuki et al., 2011). The following paragraphs will introduce pif, a well-studied SMP from the nacreous layer.
Pif, a key macromolecule for nacre formation, is translated into a large precursor and then cleaved into Pif 97 and Pif 80 via posttranslational proteolytic processing (Suzuki et al., 2009). Pif 97, containing a von Willebrand factor type A (VWA) domain, is located at the N-terminal region of the Pif protein, along with the C-terminal Pif 80, which lacks of conserved domains (Burgess and Kelly, 1987; Suzuki et al., 2013). Pif homologs have a wide distribution among various molluscs. The VWA and chitin-binding domains in Pif 97 are highly conserved even among distant species, whereas the sequences of Pif 80 are markedly different (Suzuki et al., 2013; Wang et al., 2013b). Surprisingly, Pif 80’s homolog was not detected in Pacific oyster C. gigas (Wang et al., 2013b). The laminin G domain, a Ca2+-mediated receptor, usually interacts with extracellular matrix proteins (Marin et al., 2008). The N-terminus of the laminin G domain is present between the chitin-binding domain and the C-terminus of Pif 97, while the C-terminus of the laminin G is located at the center of Pif 80, which may contribute to the CaCO3-binding activity of Pif (Suzuki et al., 2013). In C. gigas, the morphology of the inner shell surface exhibited significant changes after injection of dsRNA of Cg-Pif 97. The calcite laths of the shell became thinner and narrower along with increasing dose of Cg-Pif 97 dsRNA, indicating that the Cg-Pif 97 is indispensable during calcite shell formation in oysters (Wang et al., 2013b). Similarly, the injection of Pf-Pif dsRNA resulted in disordered growth of the nacreous layer in the pearl oyster P. fucata, suggesting that Pf-Pif might be essential for normal growth of the nacreous layer (Suzuki et al., 2009). Although lacking conserved domains, Pif 80 has some typical structural features, i.e., high proportion of charged and repetitive amino acid residues [17 repeats of Asp-Asp-Arg (Lys)-Lys (Arg) motif], which contributes to its specific binding ability to the aragonite crystals. In addition, Pif 80 is proposed to be critical in the transformation from inorganic phase to organic mineral during nacre formation. Through strong Ca2+ binding property, recombinant Pif 80 plays crucial roles in transformation from inorganic phase to organic minerals as well as regulation of aragonite crystallization during nacre formation (Bahn et al., 2017). The fraction containing Pif 80, Pif 97, and the N16 complex can induce the formation of aragonite and vaterite crystals in in vitro CaCO3 crystallization experiments, further confirming the essential roles of Pif 80 and Pif 97 during shell formation (Suzuki et al., 2009). Based on above results, the potential function of Pif during aragonite crystal formation is proposed. After first binding to chitin framework, Pif 80 and Pif 97 complex accumulates CaCO3 crystals precipitation inside the chitin membrane, and then regulates them vertical alignment.
Shell matrix proteins are generally classified according to the theoretical isoelectric point (pI). Presently, SMPs associated with nacreous layer formation are classified into two categories: moderately acidic SMPs (pI = 4.5–7, such as pif, MSI60, N16/Pearlin, N14, AP7, AP24 et al.) and basic SMPs (pI = 7–10.5, such as lustrin A, perlucin, perlustrin, perlwapin, perlinhibin, N19, N66 et al.) (Marin et al., 2008). Some SMPs of this category contain a short acidic domain, mainly participating in Ca2+ binding. Besides, other typical domains, such as VWA domain, IGF-BP domain, and C-type lectin domain, usually possess binding function. Thus it is supposed that these SMPs may be related to the extracellular microenvironment, which is critical for shell formation.
SMPs in the Prismatic Layer
The prismatic layer of mulluscan shell is mainly composed of columnar calcite crystals, which are enclosed in compact organic matrices (Carter, 1985; Chateigner et al., 2000). Lys (K)-rich mantle proteins (KRMPs) (Zhang et al., 2006b), MSI31 (Sudo et al., 1997), prismalin-14 (Suzuki et al., 2004), aspein (Tsukamoto et al., 2004), prisilkin-39 (Kong et al., 2009), P43 (Gong et al., 2008b), Alv (Kong et al., 2018), and asprich proteins (Gotliv et al., 2005; Politi et al., 2007) have been retrieved from calcitic prism textures and demonstrated to be critical in prismatic layer formation.
KRMPs represent a group of small proteins with a molecular weight of 10 kDa, and are unique to pearl oysters (P. fucata, P. maxima and P. margaritifera) (Zhang et al., 2006b; Jackson et al., 2010; Berland et al., 2011; Kinoshita et al., 2011; Mcdougall et al., 2013). KRMPs are typical basic SMPs (pI = 9.5–9.8) and rich in Lys, Gly and Tyr amino acids (Zhang et al., 2006b). Four KRMP proteins (KRMP-1 to KRMP-4), with 98-101 residues, differ only by few amino acids (Zhang et al., 2006b; Masaoka and Kobayashi, 2009). KRMPs contain two functional domains: a Lys-rich basic (BR) domain and a Gly/Tyr-rich (GYR) domain. The BR domain also exists in some other SMPs, i.e., Lustrin A (Shen et al., 1997) and MSP-1 (Sarashina and Endo, 1998), interacting with negatively charged ions or acidic SMPs. The GYR domain exhibits some homology with quinone-tanned proteins, which suggests that the Tyr residues may be oxidized in DOPA in the mature protein. KRMPs are specifically located at the mantle edge, which is recognized as the secretion zone of prismatic layer. The prismatic tablets exhibit irregular morphology after the treatment with dsRNA of KRMP. The surface of prismatic layer become lacunose and the borders between the prisms and the framework are broken along with the increased dosage (Fang et al., 2011). Furthermore, KRMP-3, retrieved from the EDTA-insoluble matrix of the prismatic layer, is located at the organic sheet and the prismatic sheath. Recombinant KRMP-3 binds tightly to chitin via the GYR domain, while the BR domain of KRMP-3 is crucial for inhibition of CaCO3 precipitation and growth of aragonite, as well as regulation of calcite morphology (Liang et al., 2015). Taken together, KRMPs are restricted to pearl oysters as well as their closest relative species, and participate in the framework formation of the prismatic layer.
Prismalin-14, is the first prismatic matrix protein identified at both protein and nucleotide levels (Suzuki et al., 2004). Prismalin-14 contains only 11 types of amino acids with a total length of 105 amino acids. Hydrophobic residues are mostly located at the interzonal region, while hydrophilic residues are distributed at both termini. The structural composition of prismalin-14 is diverse, containing a pyroglutamate, four tandem Pro-Ile-Tyr-Arg (PIYR) repeats, a Gly/Tyr-rich (GY) domain, and two Asp-rich regions at the N- and the C-termini (Takeuchi et al., 2016). The structure-function relationships of prismalin-14 have been studied through construction of recombinant proteins with different functional domains. Recombinant Prismalin-14 inhibits CaCO3 precipitation in a dose-response (Suzuki and Nagasawa, 2007; Mann et al., 2012). While ΔN (including the PIYR repeats, GY-rich, C-terminal regions) shows lower activity and ΔNΔC (including the PIYR repeats and GY-rich domain) shows hardly any inhibitory activity at the equal concentration, showing that Asp-rich domains at both termini are inhibitors of CaCO3 precipitation. In addition, the GY-rich domain is indispensable for chitin-binding activity (Suzuki and Nagasawa, 2007). Recently, transcription factor POU3F4 has been shown to directly bind the promoter of prismalin-14, and is essential for its activation function (Jing et al., 2016). Northern blot and in situ hybridization analysis show that Prismalin-14 is selectively and highly expressed at the mantle edge (Suzuki et al., 2004). Taken together, prismalin-14 acts as a scaffold which combines with chitin and CaCO3 crystals in the prismatic layer.
Aspein, the most acidic of all known SMPs (pI = 1.45), has a high ratio of Asp and is located at the mantle edge (Joubert et al., 2010). It was first identified from the mantle of P. fucata (Tsukamoto et al., 2004), and its homologs have been characterized from several other pterioid species (Isowa et al., 2012). Aspein has a signal peptide sequence (19 amino acids), which is similar to that of Asprich (63% identity), the acidic shell matrix protein identified from Atrina rigida (Gotliv et al., 2005). The expression levels of Aspein during larval and juvenile stages increase at the onset of calcite formation, while it is also weakly expressed when the shell is only composed of amorphous calcium carbonate (Miyazaki et al., 2010). Aspein especially promotes calcite precipitation via the Asp-rich domain in vitro, indicating its specific function during calcite formation (Takeuchi et al., 2008).
Except for KRMPs, other SMPs involved in prismatic layer formation share a common characteristic, namely, they are enriched in acidic amino acid residues. Thus they usually possess a relatively low pI (i.e., Aspein, pI = 1.67; MSI31, pI = 3.81; Prismalin-14, pI = 4.16; PfN44, pI = 4.25) and are categorized as extremely acidic SMPs (Marin et al., 2008). The striking finding that acidic proteins are preferentially associated with calcite in molluscan shell, was first reported in M. californianus in 1960s (Hare, 1963), which has been further confirmed with the increasing number of SMPs identified and sequenced (Marin et al., 2008; Liao et al., 2015; Kocot et al., 2016). However, the reason for this intriguing selection remains unknown. Generally, proteins with a high amount of acidic amino acid residues are negatively charged. Thus acidic SMPs should be more liable to bind Ca2+ during shell formation process. Traditionally, acquisition of acidic SMPs is not easy since they are difficult to purify. Nowadays, an increasing number of novel acidic SMPs have been identified and their corresponding primary structures also have been analyzed by virtue of genomic, proteomic and transcriptomic approaches, which will help immensely to reveal the aforementioned phenomenon, such as the preferential choice of acidic proteins associated with calcite in molluscan shell.
SMPs Involved in the Formation of Both Nacreous and Prismatic Layers
Although outer prisms and inner nacre layers in molluscan shells are assembled from very different protein repertoires, several SMPs, such as Nacrein (Miyamoto et al., 1996), MSI7 (Zhang et al., 2003; Feng et al., 2009), PfY2 (Yi et al., 2017), and shematrins (Yano et al., 2006), have reported to exert dual-function in both layers.
Nacrein, the first reported molluscan organic SMP, has a carbonic anhydrase (CA)-like domain with an insertion of Gly-X-Asn (G-X-N, X = Asp, Asn, or Glu) or Gly-Asn (G-N) repeats, and functions in both nacreous and prismatic layers (Miyamoto et al., 1996, 2005; Miyashita et al., 2002). Nacrein homologs have been identified from turban shell Turbo marmoratus (Miyamoto et al., 2003), the edible Iwagaki oyster Crassostrea nippona (Norizuki and Samata, 2008), Yesso scallop Patinopecten yessoensis (Norizuki and Samata, 2008), giant clam Tridacna gigas (Baillie and Yellowlees, 1998; Leggat et al., 2005), Pacific oyster C. gigas (Song et al., 2014), and pearl oyster P. maxima (Kono et al., 2000; Norizuki and Samata, 2008; Wang et al., 2011). The CA-like domains of the nacrein homologues share high similarity with nacrein, while the repeat sequences exhibit variability in length and composition. For example, the composition and length of repeat sequence from T. marmoratus nacrein is markedly different from that of nacrein in P. fucata and P. maxima. The former is composed of G-N two amino-acid repeat with 132 amino acids in length, while the latter is composed of G-X-N three amino-acid repeat with length of 80 amino acids (Miyamoto et al., 2003). The nacre microstructure of gastropods is in column form, whereas in sheet form in bivalves. It is speculated that the structural variance of nacrein may reflect functional difference, which may consequently lead to the production of divergent microstructures (Miyamoto et al., 2003). The structure of nacrein exhibits N-shape via small-angle X-ray scattering, which is consistent with its sequence structural features (Norizuki and Samata, 2008). Nacrein from the pearl oyster P. fucata exhibits tissue-specific expression pattern and specifically distributes at the OME (Miyamoto et al., 2005; Gong et al., 2008b). The function of nacrein during shell formation has been further demonstrated. During the in vitro experiments, the addition of recombinant nacrein protein to a saturated solution of Ca2+ and HCO3-, significantly inhibit the precipitation of CaCO3. The deletion of G-X-N repeats of nacrein significantly affects the inhibitory ability to the precipitation of CaCO3 (Miyamoto et al., 2005). Aragonite crystals exhibited aberrant growth, and aragonitic tablets became thickened when nacrein is suppressed by the antibodies (Gong et al., 2008b). It is speculated that nacrein is a negative regulator in aragonitic tablet growth, and the G-X-N or G-N repeat sequence may show inhibitory activity during CaCO3 precipitation (Miyamoto et al., 2005; Norizuki and Samata, 2008).
The novel SMP PfY2 is found in both prisms and nacre layers, suggesting its dual roles in the shell formation of P. fucata (Fang et al., 2011). The expression level of PfY2 peaks at 36 h after shell-notching, indicating its involvement of shell repairing and regenerating process. The recombinant PfY2 can significantly suppress CaCO3 precipitation rate, participate in the crystal nucleation process, and mediate the transition of amorphous CaCO3 to steady calcite or aragonite (Yi et al., 2017). The results clearly demonstrate that PfY2 is a critical macromolecule and performs a variety of biological functions during shell formation.
Shematrins, a family of Gly-rich structural proteins, is comprised of at least nine members with molecular weights of 25∼33 kDa (Yano et al., 2006; Mcdougall et al., 2013). With one exception (shematrin-5, pH = 7.7), all shematrins have a pI between 9 and 10.3, and are considered as the second family of basic SMPs. They all share characteristic primary structures and exhibit Gly-rich domains, comprised of short motifs of the type XGnX (with 2 ≤ n ≤ 6 and X = L/Y/A/V/I/M). All shematrins have a RKKKY, RRKKY or RRRKY motif at the C-terminal region (Yano et al., 2006). The Gly-rich domain of shematrin-2 is exactly identical to another acidic SMP MSI31 (98% homology in a 227 residue overlap), but their C-termini are completely different. Shematrin is strongly basic and is supposed to work as a framework for calcification, while MSI31 is extremely acidic and may be involved in nucleating crystals (Sudo et al., 1997). The C-terminal parts of shematrins exhibit a high homology (above 60% on 26 residues) with the C-terminal Gly-rich region of KRMPs (Zhang et al., 2006a). Shematrin-5 is the single protein of the family which contains an acidic domain and is similar to aspein (Tsukamoto et al., 2004). Shematrins exhibit tissue-specific expression and are located at the mantle edge. In addition, shematrin-1, -2, -3, -4, and -6 are also expressed in mantle pallial layer (Yano et al., 2006), indicating that shematrins possess dual roles in the formation of the nacreous and prismatic layers. Surprisingly, the shematrins are non-detectable in the abalone H. asinina, but exhibit active expansion and diversification within the pearl oysters, suggesting the hypothesis that the shell basic toolkit genes evolved rapidly among molluscs (Jackson et al., 2010).
Similar to the SMPs from nacreous layer, SMPs from both layers are either moderately acidic (i.e., nacrein, MSI7,) or basic (i.e., Shematrins). The functions of these SMPs show no difference between the two layers, indicating their important roles during the shell formation process.
SMPs From the Extrapallial Fluid (EPF)
Extrapallial fluid is an aqueous microenvironment located between the OME and the inner face of shell, and serves as the final medium of nacre calcification (Saha et al., 1988; Lowenstam and Weiner, 1989). EPF contains a variety of ions (Na+, K+, Ca2+, Mg2+, HCO3-), whereas the composition of ion content is different from that of the hemolymph and seawater (Saha et al., 1988; Wilt, 2002). EPF also contains various macromolecules secreted by the OME or transported from elsewhere to the EPF, such as proteins, polysaccharides, and lipids, among which the proteins are speculated to perform certain key function during shell biomineralization (Kylmaoja et al., 2016). However, largely due to the difficulty of obtaining EPF, there are few studies on the protein components. Previous studies showed that crude extraction mixtures of EPF proteins have significant influence on the morphology of crystal formation (Yin et al., 2009). Recently, amounts of novel EPF proteins have been identified by liquid chromatography-tandem mass spectrometry (LC-MS/MS) analysis of EPF proteins binding to the CaCO3 crystals (Xie et al., 2016). So far, several SMPs have been extracted from the EPF, such as EP fluid protein from M. edulis (Hattan et al., 2001; Yin et al., 2005), Amorphous calcium carbonate-binding protein (ACCBP) (Ma et al., 2007), Secreted Protein Acidic and Rich in Cysteine (SPARC) from P. fucata (Xie, 2016).
Amorphous calcium carbonate-binding protein (ACCBP) containing an acetylcholine-binding site was the first purified EPF protein from P. fucata (Ma et al., 2007). Size-exclusion Chromatography, chemical cross-linking experiments coupled with negative staining electron microscopy revealed that ACCBP is a decamer composed of two adjacent pentamers, containing two Ca0562-binding sites, which are arranged in a 5-fold symmetry. The unique structure is essential for ACC formation and affects the ACC induction efficiency (Su et al., 2013). ACCBP shows inhibitory activity on the growth of calcite and CaCO3 precipitation both in vitro and in vivo (Ma et al., 2007). Besides, ACCBP can identify diverse phases and faces of CaCO3 crystal via acetylcholine-binding site. With this capacity, ACCBP is demonstrated to alter the morphology of nacre lamellae by inhibiting the growth of certain aragonite faces, and simultaneously keep the CaCO3-supersaturated solution in steady-state by terminating the nucleation and growth of calcite (Ma et al., 2007). ACCBP mainly functions as a negative regulator during the shell formation.
Secreted Protein Acidic and Rich in Cysteine (SPARC) contain three typical functional domains (acidic region, follistatin-like region, and extracellular Ca2+-binding domain) and exist in the extracellular matrix of P. fucata (Xie, 2016). The expression levels of SPARC in EPF increase after shell-notching in P. fucata, indicating its involvement in shell repair process. SPARC is also found in both nacre and prismatic soluble extracts, and the blocking of SPARC with a polyclonal antibody was shown to inhibit the formation of nacre platelets (Xie, 2016). Furthermore, SPARC regulates the morphology of CaCO3 crystals and induces the formation of vaterite in the calcite crystallization system. However, Mg2+ counteracts this effect and induces the formation of aragonite. Further intrinsic fluorescence and circular dichroism spectrum studies indicate that SPARC may exert function by changing the conformation of its secondary structure. In conclusion, SPARC participates in nacre formation by stabilizing vaterite to inhibit calcite formation via its EC domain and secondary structure variation, as well as by assisting aragonite formation in the presence of Mg2+ or other proteins (Xie, 2016).
Compared with SMPs identified from shell, most EPF proteins perform dual roles during the transition between prism and nacre, which is closely connected with their secondary structures and specific binding capacity to calcite or aragonite. Previous results also suggest that EPF proteins play a critical role in the biomineralization balance process (i.e., shell formation and ablation) (Xie et al., 2016). Remarkably, the amino acid constituents in the EPF proteins inducing aragonite or calcite formation had different preference, which was similar with the SMPs from shell (Hare, 1963; Evans, 2008; Marie et al., 2012; Xie et al., 2016).
The Regulatory Mechanism of SMPs in Molluscs
In molluscs, their functions of more than 40 SMPs have been elucidated, while the transcriptional regulation mechanisms are poorly studied. So far, only four transcription factors, Pf-MSX (Zhao et al., 2014), Pf-AP-1 (Zheng et al., 2015), Pf-Rel (Sun et al., 2015), and Pf-POU3F4 (Jing et al., 2016), have been reported to participate in shell formation through regulating expression of SMPs in molluscs.
Pf-AP-1, Pf-MSX, and Pf-Rel, are homologous genes of MSX, AP-1, and NF-κB, which are all involved in bone/tooth formation in vertebrates (Bakiri et al., 2007; Kim et al., 2010; Saadi et al., 2013). In pearl oyster P. fucata, Pf-AP-1, Pf-MSX, and Pf-Rel could directly bind to the promoters of SMPs KRMP, Pearlin, Prisilkin-39, Pif, and nacrein, respectively, and enhances their promoter activities in a dose-dependent manner (Zhao et al., 2014; Sun et al., 2015; Zheng et al., 2015). The mRNA transcripts of KRMP, Pearlin, Prisilkin-39, Pif, and nacrein all exhibited significant depression under the treatment either with inhibitors of AP-1 and NF-κB or dsRNA of Pf-MSX and Pf-Rel (Zhao et al., 2014; Sun et al., 2015; Zheng et al., 2015). Moreover, after injection of Pf-MSX dsRNA, the lamellar sheet from nacreous layer exhibited disorder orientation (Zhao et al., 2014). Similarly, knockdown of Pf-Rel led to crystal particles on the surface of inner nacreous layer to be scattered and irregular (Sun et al., 2015), which was similar to the morphological changes when Nacrein was blocked by its antibody (Gong et al., 2008b). A putative AP-1 binding site was predicted at the 5′-flanking region of the nacrein gene, and human AP-1(c-jun) has been reported with regulatory function in nacrein transcription in vitro (Miyashita et al., 2012). However in P. fucata, the expression pattern of nacrein showed almost no correlation with Pf-AP-1, and the inhibitor of AP-1 (SR11302) had no effect on the expression of nacrein (Zheng et al., 2015). In vertebrates, transcription factor POU mainly functions in the neuroendocrine system (Andersen and Rosenfeld, 2001). In molluscs, homolog of POU3F4 (Pf-POU3F4) has been identified and demonstrated to participate in shell formation through binding to the promoters of SMPs Aspein and Prismalin-14, and enhancing their transcriptional activities (Jing et al., 2016).
It is evident that some conservative transcription factors such as AP-1, MSX, and Rel, share similar function among diverse animals, playing important roles in bone/teeth formation in vertebrates and shell formation in molluscs. The distinct functions of POU between mammals and molluscs also suggest that there exist unique features in the regulation mechanism of shell formation in molluscs. So far, most results were obtained from transfection experiments in vitro; more direct evidence within primary culture of molluscan cells will be further highlighted in the future.
The Rapid Evolution of SMPs in Molluscs
Molluscs began to mineralize at the dawn of the Cambrian times, in a very short time interval, about 544 million years ago (Conway Morris, 2001). Like several other metazoan phyla, molluscs acquired the capacity to form a mineralization exoskeleton far after their emergence as a phylum, implicating that the ‘molecular tool box’ required for mineralizing is produced and employed. However, the mechanisms underlying production of calcified shell, whether originated from an ancestral biomineralization repertoire, or the production of lateral genetic transfer, are still unclear (Marin et al., 2008). The recent sequencing of several mollusc genomes coupled with the analysis of multi-omics demonstrates that many SMPs evolved independently and the shell proteome may have a much higher plasticity than expected.
The highly complex, robust and patterned shells are diverse among molluscs. Conventionally, the diverse of shell types can best be expressed by the diversity secretory repertoires from outer fold of mantle organ. One might expect that the representative characteristics of shell are reflected by evolutionary changes of SMPs. Recent multi-omics studies have revealed the existence of tremendous diversity in the mantle secretomes. For example, a comparative scan between the obtained EST sequences of the abalone H. asinina and the genome of the patellogastropod Lottia scutum, shows that only 19% of the secreted proteins of H. asinina have their homologues in L. scutum (Jackson et al., 2006). Less than 15% of the secreted proteins are shared between a bivalve (P. maxima) and a gastropod (H. asinina), by comparing their nacre-secreting mantle transcriptomes (Jackson et al., 2010). In addition, a large proportion of novel secreted proteins are identified in the shell proteomes of L. gigantea when searched in the public databases. Few homologous proteins (1.1 to 7.7%) are found between any two molluscan species (Marie et al., 2013). Interestingly, the number of homologous SMPs shared between different classes is more than that between the same class, based on the comparison of the mantle transcriptomic of L. gigantea, P maxima, and H. asinina (Jackson et al., 2010). In addition, SMP genes are reported to be frequently duplicated in the Pinctada and Lottia genome (Marie et al., 2013; Takeuchi et al., 2016). For example, five genes of the shematrins tandemly cluster in two scaffolds. Three and two transcripts of N19 and N16 locate at same scaffold, respectively. Amazingly, homologous to shematrin, N19 and N16 are not detected in the C. gigas genome (Miyamoto et al., 2013; Takeuchi et al., 2016). Thus it could be concluded that these SMP genes are unique to the P. fucata lineage, and duplication occurred after speciation.
The acid-insoluble matrices (AIMs) associated with prismatic and nacreous layers are extremely different. Prism AIM is rich in Tyr, Pro, and Val, while nacre AIM contains more Ala and Asx (Asn and Asp). Eighty different SMPs have been identified between prismatic and nacreous layer, among which 64 are entirely unique (Marie et al., 2012). In Pinctada spp., 47/50 prism-related proteins are restricted to prisms, while 30/33 nacre-related proteins, are unique to nacre. A high ratio of the analyzed 61 transcripts were selectively overexpressed at the edge or pallium cells of the mantle organ, which is in line with the protein distribution either in prism or in nacre (Marie et al., 2012). Homologs of aragonite-and calcite-associated SMPs were searched through the oyster genome. Surprisingly, homologs of calcite-associated SMPs were non-detectable (0/29), while nine homologs of aragonite-associated SMPs are identified in the oyster genome (9/28). Since the oyster shell mainly is composed of calcite crystal, only the zone of the adductor muscle scar is composed of aragonite (Lee et al., 2011). Thus, aragonite-associated SMPs may be more conserved than the calcite-associated SMPs in the Molluscs.
Repetitive, low-complexity domains (RLCDs), in particular Gly-rich structural proteins, usually existed in tough, extracellular structures, and also have been identified in molluscan shell, such as KRMP (Masaoka and Kobayashi, 2009) and shematrin (Yano et al., 2006). Previous studies suggest that KRMPs and shematrins have large paralogous genes (at least 11 KRMPs, and 9 shematrins) in Pinctada spp., but show significant sequence divergence among orthologous genes, supporting the hypothesis that many SMPs are rapidly evolving (Yano et al., 2006; Masaoka and Kobayashi, 2009). RLCDs usually function in structure construction, and appear to evolve rapidly under selective pressures through Metazoans (Smith-Keune and Jerry, 2009). Therefore, it is proposed that the rapid evolution of KRMPs and shematrins probably arise from the RLCDs, which usually endow new mechanical properties with the structure they comprise (Jackson et al., 2010; Mcdougall et al., 2013).
The recent availability of complete genome data for several molluscs (Zhang et al., 2012; Takeuchi et al., 2016; Du et al., 2017; Nam et al., 2017; Wang et al., 2017), and the vastly increasing transcriptome, proteome, and secretome data, enable identification of more novel SMPs, and to comparatively study the origin and evolution of biomineralization in molluscs. Existing results reveal that SMPs are divergent in different molluscs, consistent with the heterogeneity of shell microstructures, which is constructed from a rapidly evolving secretome and has evolved convergent. However, since lack of steady cell line, the functions and transcription regulation of most SMPs have been investigated using in vivo experiments, which cannot truly reflect the interaction among SMPs under physiological conditions. More insight into the true functions of SMPs should be obtained either via in vitro cell culture system from molluscs or in vivo reverse genetics, such as RNAi or CRISPR/Cas9 genome editing technique.
Hemocyte-Mediated Shell Mineralization in Molluscs
Hemocytes are essential during the innate immune response, which has been shown to be related to biomineralization in molluscs. For example, amounts of hemocytes accumulate in the pearl sac after transplantation in pearl oyster (Kishore and Southgate, 2015). Immune-associated genes also exhibit significant expression during the shell regeneration period in Laternula elliptica (Sleight et al., 2015). Recently, more evidence directly demonstrated that hemocytes (mainly granulocytes) participate in the synthesis and delivery of CaCO3 crystals as well as SMPs during the shell regeneration process (Mount et al., 2004; Mount and Pickering, 2009; Cho and Jeong, 2011; Johnstone et al., 2015; Li et al., 2016).
Shell damage-repair is a routine method to study shell formation. During shell regeneration, granulocytes have been shown to participate in the synthesis and transportation of CaCO3 (Mount et al., 2004; Johnstone et al., 2015). The granular inclusions of hemocytes are Ca2+-positive in the green ormer H. tuberculata (Fleury et al., 2008), Pacific oyster C. gigas (Ivanina et al., 2017), deep-sea mussel Bathymodiolus azoricus (Kadar et al., 2009), and pearl oyster P. fucata (Li et al., 2016), suggesting that the granulocytes may be a calcium pool and act as a calcium conveyor during shell formation (Kadar et al., 2009; Cho and Jeong, 2011). Intracellular CaCO3 crystals are observed in hemocytes of various shelled molluscs. For example, x-ray microanalysis (SEM-EDS) reveals that crystal-shaped inclusions with rhombohedral appearance are enclosed in the refractive granulocytes (REF granulocytes), a subclass of granulocytes in Eastern oyster C. virginica. Some REF granulocytes have only one or two crystals, while others have numerous (Mount et al., 2004). Crystal-like structures with various shapes are also observed in granulocytes of P. fucata, but one crystal could be only found in one cell. The chemical components of crystal-like structures were analyzed via SEM-EDS, which mainly contain Ca, C, O2, P, and Si, similar to natural CaCO3 crystals (Li et al., 2016). There are varied shapes of the crystals in P. fucata, but only hexahedron crystals are observed in C. virginica. Furthermore, REF cells are present on the prismatic shell surface in lines with fibrous materials and crystals (Mount et al., 2004). Similarly, the granulocytes are embedded into the column and fragmentation of matured shell, which was observed in oyster C. gigas (Cho and Jeong, 2011) and P. fucata (Li et al., 2016), directly showing that living hemocytes are present at the mineralization front. In addition, a highly refractive structure is detected in the hemocytes of B. azoricus induced by shell damage (Kádár, 2008), and insoluble CaCO3 is synthesized in the hemocytes of Venerupis philippinarum during the initial period of shell regeneration (Trinkler et al., 2011). The crystal bearing hemocytes present in the EPF of the oyster C. virginica and the mussel B. azoricus, are able to start CaCO3 crystal nucleation in vivo (Kadar et al., 2009; Cho et al., 2011). Remarkably, after incubation with EPF mixture, the hemocytes in Pacific oyster C. gigas produce numerous spherical calcium granules, which are almost identical in morphology and chemistry to those on the regenerated shell, suggesting the involvement of hemocytes during the regeneration of prismatic layer (Cho and Jeong, 2011). Given that the prismatic layer locates outside the calcified shell and is first produced during biomineralization, the granulocytes may participate in the initiating process of shell biomineralization. The involvement of hemocytes in the nacreous layer formation remains concern.
Besides to crystal synthesis and transport, the hemocytes are reported to function in the organic framework formation. Multi-omics data reveal that various SMPs are highly expressed in the hemocytes of various shelled molluscs. For example, SMPs (e.g., Shematrin 2 and ACCBP) and Ca2+ binding proteins α-subunit are abundant in the hemocytes of P. fucata (Liao et al., 2015; Li et al., 2016). In the Pacific oyster C. gigas, several shell formation related genes, i.e., chitin synthases, nacrein-like protein, casein kinases, VEGF and VEGF-R, are highly expressed in H2 and H3 hemocytes (kinds of larger, irregularly shaped cells, similar to granulocytes), which are potential players in biomineralization processes (Ivanina et al., 2017). SMPs were visualized in molluscan hemocytes during the shell repair process, suggesting the contribution of hemocytes to the formation of the shell framework (Shitalbahen, 2004; Johnstone et al., 2008). For example, SMP coated with collagen fibers were secreted from hemocytes of the Eastern oyster, C. virginica during the shell repair process (Shitalbahen, 2004). A 48 kDa SMP has been localized in hemocytes, but is unobservable after induction of shell repair (Johnstone et al., 2008). It is reported that circulating hemocytes can internalize the antigen when exposed to a hemocyte-free EPF liquid (Calvoiglesias et al., 2016). Due to limited knowledge, the specific function of hemocytes during the secretion and transportation of SMPs needs further investigation.
In conclusion, there is a suitable microenvironment in hemocytes of molluscs for depositing CaCO3 crystal. Hemocytes might play crucial roles during shell formation by regulating the in vivo formation of CaCO3 crystals, transferring the crystals via the EPF to the regenerated prismatic layer, assisting SMPs to form crystal template. The hemocyte might function in immune response with the similar role during soft tissue repair. More focus of the hemocytes function during the larvae ontogenesis, the demineralization, abnormal biomineralization as well as nacreous layer formation, would be helpful to investigate the hemocyte-mediated shell mineralization in molluscs.
The Potential Cellular Model and Mechanism of Shell Biomineralization
The mechanisms of shell formation have been investigated over the past several decades. Calcite and aragonite are two common polymorphs in molluscan shell structure, which mainly differ in the organization and orientation of the carbonate molecules (Stenzel, 1963). Hare (1963) indicated the composition difference of organic matrices in aragonite and calcite, and thus proposed that the organic matrix proteins might be responsible for the formation of various shell structures and mineral phases. It was reported that the addition of excessive Mg2+ (400 mg/500 ml) promotes the accumulation of aragonite in CaCO3 solutions during in vitro experiments (Tokuyama, 1969), suggesting that the concentration of ions (in particular Mg2+) in the precipitating solution could regulate the polymorphism between aragonite-calcite in molluscan shell (Blackwelder et al., 1976; Wilbur and Bernhardt, 1984). In order to determine the significance of organic matrices, especially the proteins that function in shell formation, Falini et al. (1996) reassembled a substrate in vitro composed of β-chitin and silk fibroin for crystal nucleation. They found that proteins extracted from the aragonitic- and calcitic- shell layers could mainly induce aragonite and calcite formation in vitro, respectively (Falini et al., 1996). A large number of subsequent studies support the matrix-mediated shell formation hypothesis, and it has been widely believed that shell calcification occurs in mantle-secreted compartments of chitin, silk fibroin and matrix proteins, and the matrix proteins are associated with the mineral phase and influence on crystal growth (Watabe, 1965; Addadi et al., 2006; Furuhashi et al., 2009). The first observation of hemocytes at the mineralization front using vital fluorescent staining and SEM raised the cellular basis for shell formation (Mount et al., 2004). Secretome and transcriptome data reveal that some SMPs are non-secretory, and some others were abundant in other tissues (Marie et al., 2010, 2012; Kinoshita et al., 2011; Mann et al., 2012; Wang et al., 2013a). Furthermore, biominerals and SMPs are observed in the hemocytes (Johnstone et al., 2008; Calvoiglesias et al., 2016), and hemocytes as well as OME assembling on the surface of regenerated prismatic layer (Cho and Jeong, 2011; Johnstone et al., 2015; Kong et al., 2015), prompt us to investigate the mechanism of shell formation from cellular aspects. The hypothesis that co-operative interaction of hemocytes and OME during shell formation have been developed (Figure 1).
Most SMPs are produced and secreted by the OME, while a few SMPs are produced from hemocytes or other organs (Miyamoto et al., 2013; Wang et al., 2013a). The SMPs produced by the OME will be directly delivered to the crystallization surface via exosome (Zhang et al., 2012) or classical secretory pathway, while those produced from other organs are first transported to the hemolymph via classical or non-classical secretory pathways (Gardella et al., 2002), then engulfed by hemocytes (mainly granulocytes). The CaCO3 crystal either produced in the mantle or synthesized in hemocytes (granulocytes) will be delivered to the biomineralization front via the EPF (Mount et al., 2004; Weiner and Addadi, 2011; Li et al., 2016). The organic matrix or mucus secreted from OME can load with Ca2+ and deliver them to the biomineralization front via the EPF (Fleury et al., 2008; Kadar et al., 2009). During the shell regeneration process, the granulocytes are embedded into the columns of the prismatic layer, and interact with SMPs, or with polysaccharide or chitin, to construct the shell framework. CaCO3 crystals discharged from hemocytes (granulocytes), organic matrix or mucus, are subsequently deposited on the calcite of the prismatic layer (Wang et al., 2013a; Li et al., 2016).
Concluding Remarks
Biomineralization occurs widely in nature, and the shell formation of molluscs is considered as a good model of this process. The molluscan shells are produced under a series of sophisticated regulation steps involving cells (OME and hemocytes) and cell products (macromolecules mainly including SMPs, chitin and silk fibroin). The coordination between them reveals the cellular and molecular mechanism of biologically controlled mineralization. Multi-omics analyses together with molecular biology techniques has unveiled novel findings, i.e., the diversity of SMPs and significant variation between different SMP repertoires, the multiple-organ origin of SMPs, and the involvement of hemocytes in the formation of prismatic layer. These findings illustrate the complicated processes during shell formation, which will prompt a more detailed investigation on biomineralization in molluscan shell. Recent research have found that shell extracts from M. edulis and C. gigas promote the catabolic pathway of primarily cultured human dermal fibroblasts, which might be helpful in the context of anti-fibrotic strategies, particularly against scleroderma. Future studies in shell formation of molluscs are likely to uncover potential links to immunity as well as human disease, thus revealing a better understanding of the evolution of biomineralization.
Author Contributions
XS and ZL collected the literature and prepared the manuscript. LW and LS revised the manuscript. LS designed the manuscript.
Funding
The work is supported by a grant (No. U1706204) from National Science Foundation of China, and earmarked fund (CARS-49) from Modern Agro-industry Technology Research System, AoShan Talents Cultivation Program Supported by Qingdao National Laboratory for Marine Science and Technology (No. 2017ASTCP-OS13), Key R&D Program of Liaoning Province (201703165), and the Fund for Outstanding Talents and Innovative Team of Agricultural Scientific Research.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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Keywords: biomineralization, outer mantle epithelial cells, shell matrix proteins, hemocytes, marine molluscs
Citation: Song X, Liu Z, Wang L and Song L (2019) Recent Advances of Shell Matrix Proteins and Cellular Orchestration in Marine Molluscan Shell Biomineralization. Front. Mar. Sci. 6:41. doi: 10.3389/fmars.2019.00041
Received: 16 February 2018; Accepted: 28 January 2019;
Published: 19 February 2019.
Edited by:
Vera Bin San Chan, Clemson University, United StatesReviewed by:
Vengatesen Thiyagarajan, The University of Hong Kong, Hong KongGary H. Dickinson, The College of New Jersey, United States
Copyright © 2019 Song, Liu, Wang and Song. 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) and the copyright owner(s) 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: Linsheng Song, lshsong@dlou.edu.cn