Dong Fu- Faculty of Pharmacy, The University of Sydney, Sydney, NSW, Australia
P-glycoprotein (P-gp), an ATP-binding cassette, is able to transport structurally and chemically unrelated substrates. Over-expression of P-gp in cancer cells significantly decreases the intercellular amount of anticancer drugs, and results in multidrug resistance in cancer cells, a major obstacle in cancer chemotherapy. P-gp is mainly localized on the plasma membrane and functions as a drug efflux pump; however, P-gp is also localized in many intracellular compartments, such as endoplasmic reticulum, Golgi, endosomes, and lysosomes. P-gp moves between the intracellular compartments and the plasma membrane in a microtubule-actin dependent manner. This review highlights our current understanding of (1) the intracellular localization of P-gp; (2) the traffic and cycling pathways among the cellular compartments as well as between these compartments and the plasma membrane; and (3) the cellular factors regulating P-gp traffic and cycling. This review also presents a potential implication in overcoming P-gp-mediated multidrug resistance by targeting P-gp traffic and cycling pathways and impairing P-gp localization on the plasma membrane.
Introduction
P-glycoprotein (P-gp), a 170 kDa membrane protein, is a member of sub-family B of the ATP-binding cassette (ABC) transporter superfamily, and is also called ABCB1. P-gp has two structurally identical halves. Its N-terminal half contains six transmembrane domains, followed by a large cytoplasmic domain with an ATP-binding site. Similarly, the C-terminal half also has six transmembrane domains and an ATP-binding site (1, 2). Plasma membrane located P-gp is able to transport many chemically and structurally unrelated substrates out of the cells, and acts as an efflux pump (1, 2). P-gp is primarily expressed in the liver, kidney, gastrointestinal tract, and blood brain barrier. P-gp is located on the canalicular apical membrane of hepatocytes in the liver; on the brush border of proximal tubule cells in the kidney; and on the apical membrane of mucosal cells in the small intestine (3). Given the transporting function of P-gp, these tissue distributions allow P-gp to excrete endogenous metabolites, exogenous substrates, and toxins into the urine, bile, and feces. Thus, P-gp can protect the organism as well as eliminate cellular wastes (3, 4). Furthermore, another essential localization of P-gp is on the luminal surface of capillary endothelial cells of the blood brain barrier which prevents cytotoxins from penetrating the endothelium and protects brain (5).
Although animal well-being, normal physiological function, and life span were not affected after P-gp was knocked out in mice, higher drug sensitivity and increased drug side effect/toxicity occurred (6). While knocking out P-gp appears to be less problematic, over-expression of P-gp causes major concerns in clinical oncology. The most notable consequence of over-expression of P-gp in clinic is to cause multiple drug resistance (MDR) in cancer chemotherapy (2). Given P-gp has a structurally broad range of substrates, the occurrence of MDR during chemotherapy is one of the big challenges for successful cancer treatment in clinic. MDR can be either intrinsic, occurring in cancers that have not been exposed to chemotherapy before but derived from tissue naturally expressing P-gp (e.g., liver, kidney, intestinal cancers), or required MDR, which develops after cancers are treated with chemotherapy (7). Nearly half of human cancers express P-gp at levels sufficient to develop MDR. The likelihood of failure in chemotherapy is increased when P-gp expression is upregulated during therapy (8).
Intracellular Localization of P-gp
P-glycoprotein is primarily localized on the plasma membrane for its efflux function, however, it is also localized intracellularly (9, 10). Using immunofluorescence and over-expression of P-gp-GFP fusion protein approaches, co-localization results revealed that P-gp is localized in many cellular organelles, including endoplasmic reticulum (ER) (9), Golgi (9), early endosome (11–13), recycling endosome (12), later endosome, lysosome (9, 11), and proteasome (14) (Figure 1). These intracellular localizations link to synthesis (ER), modification (Golgi), traffic/recycling (Golgi and endosomes), and degradation (lysosome and proteasome) sites for P-gp. Although one study suggests P-gp is also located in mitochondria in doxorubicin-resistant K562 human leukemia cells (15), others reveal that P-gp is not presented in mitochondria either in MCF-7 (ADR) human breast cancer and KB-V1 human cervix carcinoma drug resistant cell lines (16) or in primary rat hepatocytes (17). Furthermore, transient transfection of P-gp-GFP in cancer cells reveals that the ER and Golgi localization of P-gp appears to be transient, suggesting that P-gp can rapidly traffic to the endosomal compartment and the plasma membrane localization after it is synthesized in ER and modified in Golgi. This rapid transport to the membrane localization explains why less ER or Golgi localization can be observed in the stable cell line which is overexpressed with P-gp-GFP. It is possible that activity of P-gp synthesis remains at a relatively low level due to the very long half-life of P-gp (14–17 h) in the stable cell line (18). Similarly, the degradation localization (lysosome) also appears to be less common within the cells compared to the endosomal localization which is involved in constantly trafficking/recycling P-gp between the cellular pool and the plasma membrane (11).
Figure 1. Intracellular localization, traffic, and recycling of P-glycoprotein. P-gp is shown as “green dot 
.” Different Rab GTPases that are involved in P-gp traffic and recycling are indicated as “black diamond 
.” Arrows represent the traffic and recycling path among the intracellular organelles and between the cellular organelles and the plasma membrane.
Intracellular Traffic and Recycling of P-gp
After synthesis in ER, P-gp first needs to be correctly folded before exit from ER and entry to Golgi for modification. Currently, very little information is available about the exact regulatory process for P-gp folding in ER. Glycoprotein glucosyl transferase (UGGT) is able to sense the folding states of glycoproteins, resulting in mis-folded glycoprotein rebinding calnexin (a chaperon for protein folding) and going through re-folding cycles or being rapidly degraded via endoplasmic-reticulum-associated protein degradation (ERAD) (19). Thus, UGGT may play a potential role in recognizing the folding of P-gp. Moreover, a study suggests that SPTLC1 (Serine palmitoyltransferase enzyme 1) is able to interact with ABCA1 and cause ER retention of ABCA1, revealing the role of SPTLC1 in ER exit of ABC transporters (20). Furthermore, the formation of disulfide bonds is a critical step in the maturation of the majority of the proteins inside ER (21). Studies showed that two other ABC transporters, ABCB6 and ABCC8, form the disulfide bonds between highly conserved cysteine, which is important for these ABC transporters to exit ER and traffic to the plasma membrane (22). We still lack direct evidence of how P-gp export at the ER – the first step of its trafficking along the biosynthetic secretory pathway. In mammalian cells, the ER export occurs via Coat Protein II (COPII)-coated vesicles. COPII vesicles bud from the ER and are able to fuse to ER-Golgi intermediated compartment (23). Studies reveal that COPII plays an essential role in exporting ABCB1 and ABCC7 (cystic fibrosis transmembrane conductance regulator, CFTR) from ER to Golgi (24, 25), suggesting COPII may regulate ER export of P-gp as well. Golgi is involved in the biosynthesis of glycan chains of glycoproteins, the 150 kDa P-gp is transported to the Golgi and glycosylated as the 170 kDa mature protein (26) (Figure 1).
After its modification in Golgi, the 170 kDa mature P-gp traffics to the plasma membrane. Membrane proteins can traffic to the plasma membrane via either the constitutive pathway which involves membrane protein-containing vesicles moving directly to the plasma membrane (27, 28) or the endosomal pathway in which protein-containing vesicles are first transported to endosomal compartments to establish the intracellular pool, and then traffic to the plasma membrane (29). In both cases, the cytoskeleton is needed for the traffic of these membrane protein vesicles (30). The trans-Golgi network (TGN) is a major sorting site for proteins trafficking to the plasma membrane and endosomal pathway. A study suggests that membrane proteins use N-glycan chains as sorting determinants (31); whether this also applies to P-gp needs to be investigated. However, some studies show that N-glycosylation at amino acid residue asparagine 596 at third extracellular loop is not necessary for ABCG2 traffic (32), and the immature core-glycosylated CFTR (ABCC7) can be transported to the plasma membrane and is functional (33).
In the non-polarized cancer cells, P-gp was reported localized in EEA1 and Rab5 positive early endosome which serves as an intracellular reservoir prior to P-gp moving to the plasma membrane (11), suggesting that P-gp can traffic to the plasma membrane via the indirect endosomal pathway. Furthermore, immunofluorescence study showed that P-gp is also localized in lysosome after transient expression of human P-gp-GFP in HeLa cells or in the human breast cancer MCF-7 cells, which are stably expressed with P-gp-GFP, suggesting P-gp can be moved to the lysosomal degradation compartment, presumably through the early and late endosome (12). However, an immunofluorescence study reveals that P-gp is not localized in Rab11 positive recycling endosomes in human breast cancer MCF-7 cells, which stably express P-gp-GFP (11). In the polarized WIFB9 cells as well as hepatocytes, apical ABC transporters (e.g., P-gp, ABCB11) move to the apical membrane via Rab11a recycling endosomes and recycle between the apical membrane and the Rab11a positive intracellular endosomal pool (29, 34) (Figure 1). These studies suggest that P-gp traffics and recycles via different endosomal pathways (early endosome vs. recycling endosome) in non-polarized cells (e.g., cancer cells) and polarized cells.
Regulation of P-gp Traffic and Recycling – Role of Rab GTPases
Rab GTPases, the largest branch of small GTPase, are known to regulate vesicular transport in exocytosis, endocytosis, and recycling by controlling many steps in membrane trafficking such as vesicle formation, movement, uncoating, docking, and fusion (35). So far more than 70 Rab GTPases have been identified in humans (35). Each Rab protein is believed to be specifically associated with a particular organelle or pathway (35). Currently, few studies revealed the role of Rab proteins in P-gp trafficking, thus, the more general involvement of Rab proteins in ABC transporters trafficking and recycling will be discussed.
Rab1, 2, and 6 are localized in ER and Golgi and regulate vesicle transport along the ER-Golgi biosynthetic pathway. Rab1, 2 regulate vesicle movement from ER to Golgi (35, 36), while Rab6 is involved in Golgi to the cell surface for exocytosis of newly synthesized proteins and lipids (37). Study showed that P-gp was predominantly intracellular, largely in Rab6-containing Golgi vesicles and Golgi cisternae (7), suggesting Rab6 may regulate P-gp traffic directly from Golgi to the plasma membrane (Figure 1).
Along the endosomal trafficking pathway, Rab11 and Rab13 are involved in membrane protein traffic from Golgi to the recycling endosome (38–40). Rab11a was shown to regulate P-gp and ABCB11 traffic to the apical membrane in polarized WIFB9 cells (29, 34) (Figure 1). Furthermore, studies showed that Rab11a was also needed for both WT-CFTR and ΔF508-CFTR to undergo trafficking to the apical recycling compartment in polarized human airway epithelia cells (41) as well as polarized intestinal epithelial cells (42). These studies reveal that, in polarized cells, P-gp traffics to the apical membrane via the Rab11a positive recycling endosome. However, in non-polarized MCF-7 cells, stable expressed P-gp-EGFP did not co-localize with Rab11 positive recycling endosome (11), suggesting P-gp does not traffic to the cell surface via the Rab11a positive recycling endosome. Evidence indicates that membrane trafficking of CFTR is cell type-specific and it differs in polarized human airway epithelial cells such as CFBE41o- cells and in non-polarized fibroblasts such as BHK-21 cells (41). Thus, Rab11a may have a differential role in P-gp trafficking in non-polarized and polarized cells. Other Rab proteins, such as Rab17, Rab25, Rab35, and Rab40 are also localized in recycling endosome (36, 43). Rab35 is shown to play important role in insulin-stimulated GLUT4 (Glucose transporter type 4) translocation in adipocytes (44). Further studies are needed to investigate the role of Rab11 as well as other Rab proteins (e.g., Rab17, Rab25, Rab35, and Rab40) in P-gp traffic in both polarized and non-polarized cells.
Early endosomal pathway is shown to be involved in P-gp trafficking and recycling. Among many of the early endosomal Rab proteins, Rab4 and Rab5 are known to regulate P-gp trafficking and recycling in many cancer cells (12, 13, 45). Over-expression of dominant-negative Rab5 mutant (S34N-Rab5) results in large intracellular accumulation of P-gp-EGFP in non-polarized Hela cells, and similar cellular accumulation of wild type P-gp in multidrug resistant MCF-7/Adr cells, revealing that Rab5 regulates P-gp exocytosis from the endosome compartment (such as early endosome) to the plasma membrane in non-polarized cells (12). In contrast, another study in colon cancer cells LS174T, demonstrated that over-expression of wild-type Rab5 resulted in recycling P-gp from the plasma membrane into intracellular compartments, suggesting that Rab5 regulates P-gp endocytosis instead of exocytosis (13), however, this study did not investigate the polarization status of the cell culture of LS174T, which is shown to be polarized in normal culture condition (46). Thus, the differential role of Rab5 in P-gp trafficking and recycling in these cancer cells may be related to the difference in polarization (Figure 1).
Rab4 is also localized in early endosome and shown to regulate P-gp exocytosis in drug resistant leukemia cells, K562ADR (45). Cell surface expression of P-gp decreased after over-expression of GFP-Rab4 or constitutively active Rab4Q72L mutant, but not dominant-negative Rab4S27N mutant or Rab14 in the K562ADR cells, suggesting that Rab4 regulates P-gp trafficking to the plasma membrane from endosomal compartments (45). However, in HeLa cells, the intracellular localization of P-gp-EGFP was not affected when there was over-expression of either wild-type Rab4 or dominant-negative mutant N121I-Rab4 respectively (12), indicating Rab4 does not effect P-gp trafficking. The different cell lines used in these studies may be the reason for obtaining different results. Given many other Rab proteins, such as Rab10, 14, 15, 17, 22, and 23 are localized on early endosome (43), it is likely these Rab proteins can also regulate the trafficking and recycling of P-gp between the early endosomal compartment and the plasma membrane in a cell and tissue type-specific manner.
Transmembrane proteins can be transported from late endosome to lysosome which is responsible for degradation of the membrane proteins (47). P-gp is localized in Lamp-2 positive lysosome, revealing its lysosomal dependent degradation pathway (11). Rab7 is localized on late endosome and lysosome, and is essential for later endocytic membrane trafficking from late endosome to lysosome (48, 49), while Rab9 is localized on later endosome and responsible for transit from later endosome to the TGN (50). Although very little is known about the role of Rab7 and 9 on later endocytic membrane trafficking of P-gp, Rab7 and 9 are shown to regulate other ABC transporter trafficking (e.g., CFTR). Using over-expression of wild type and mutant Rab GTPases, a study revealed that CFTR could enter Rab7-dependent late endosomal traffic or Rab9-mediated translocation to the TGN (51), suggesting the role of both Rab7 and 9 in later endocytic trafficking of CFTR. However, the potential roles of Rab7 and 9 on P-gp trafficking need to be investigated (Figure 1).
Clinical Implications
P-glycoprotein plays an important role in drug excretion and is one of the main causes for MDR in cancer chemotherapy. Different generations of P-gp inhibitors are developed and enter into preclinical and clinical studies. The first generation of P-gp inhibitors, such as verapamil and cyclosporin A, are active substrates of P-gp. Both verapamil and cyclosporin A cause side effects in patients due to high dose of the drugs are need for their inhibition of P-gp (52, 53). The second generation of P-gp inhibitors include valspodar (PSC 833), dexverapamil, and dofequidar fumarate. However, these second generation inhibitors also inhibit drug metabolism enzymes and other ABC transporters, which results in impaired drug metabolism and elimination (54–56). The third generation of P-gp inhibitors, which are currently undergoing clinical trials, include zosuquidar (LY335979), elacridar (GF120918), CBT-1, and XR9576 (57–60). However, some of the trials are unsuccessful in improving therapeutic efficacy (61). For example, trial was stopped in patient with non-small-cell lung cancer due to chemotherapy-related toxicity after administration of XR9576 (60). Thus, there is an urgent need to develop innovative strategies to overcome P-gp-mediated MDR in cancer chemotherapy.
Given P-gp needs to be transported to the plasma membrane so as to efflux the anticancer drugs out of cells, blocking the trafficking of P-gp to its final destination – the plasma membrane location – can be an innovative approach to overcome MDR and improve therapy. There are multiple potential targets along the P-gp traffic pathway. Study revealed that inhibition of P-gp maturation resulted in accumulation of P-gp in Golgi, and this immature P-gp in Golgi was inactive and presumably led to degradation. Consequently there was an increased cellular accumulation of P-gp substrate (62). Experiments also reveal that blocking P-gp traffic to the plasma membrane by interrupting the cytoskeleton highway or modulating Rab activation can cause increased intracellular accumulation of P-gp, resulting in more intracellular retention of anticancer drug (9, 11, 12). Although the intracellular P-gp that is trapped on the way to the plasma membrane remains active, it is likely that intracellular P-gp do not contribute to drug resistance (63). It is essential to identify the regulatory effectors, such as specific Rab GTPases or Rab binding proteins for P-gp traffic and recycling, and to screen potential candidates for targeting these effectors. Therefore, more studies are needed to understand the molecular and cellular mechanisms of P-gp intracellular traffic/cycling and its regulatory factors.
Conflict of Interest Statement
The author declares 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: P-glycoprotein, intracellular localization, traffic, recycling, cell polarization, multidrug resistance in cancer
Citation: Fu D (2013) Where is it and how does it get there – intracellular localization and traffic of P-glycoprotein. Front. Oncol. 3:321. doi: 10.3389/fonc.2013.00321
Received: 28 October 2013; Accepted: 17 December 2013;
Published online: 30 December 2013.
Edited by:
Stefania Nobili, University of Florence, ItalyReviewed by:
Brion William Murray, Pfizer Oncology Research Unit, USAAmit K. Tiwari, Tuskegee University, USA
Copyright: © 2013 Fu. 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: Dong Fu, Faculty of Pharmacy, The University of Sydney, Building A15, Sydney, NSW 2006, Australia e-mail: dong.fu@sydney.edu.au