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J. Biol. Chem., Vol. 279, Issue 50, 52735-52743, December 10, 2004
ADP-ribosylation Factor 1-independent Protein Sorting and Export from the trans-Golgi Network*![]() From the Laboratory of Epithelial Cell Biology, Renal-Electrolyte Division, Department of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania 15261
Received for publication, September 13, 2004 , and in revised form, September 29, 2004.
Polarized epithelial cells efficiently sort newly synthesized apical and basolateral proteins into distinct transport carriers that emerge from the trans-Golgi network (TGN), and this sorting is recapitulated in nonpolarized cells. While the targeting signals of basolaterally destined proteins are generally cytoplasmically disposed, apical sorting signals are not typically accessible to the cytosol, and the transport machinery required for segregation and export of apical cargo remains largely unknown. Here we investigated the molecular requirements for TGN export of the apical marker influenza hemagglutinin (HA) in HeLa cells using an in vitro reconstitution assay. HA was released from the TGN in intact membrane-bound compartments, and export was dependent on addition of an ATP-regenerating system and exogenous cytosol. HA release was inhibited by guanosine 5'-O-(3-thiotriphosphate) (GTP S) as well as under conditions known to negatively regulate apical transport in vivo, including expression of the acid-activated proton channel influenza M2. Interestingly, release of HA was unaffected by depletion of ADP-ribosylation factor 1, a small GTPase that has been implicated in the recruitment of all known adaptors and coat proteins to the Golgi complex. Furthermore, regulation of HA release by GTP S or M2 expression was unaffected by cytosolic depletion of ADP-ribosylation factor 1, suggesting that HA sorting remains functionally intact in the absence of the small GTPase. These data suggest that TGN sorting and export of influenza HA does not require classical adaptors involved in the formation of other classes of exocytic carriers and thus appears to proceed via a novel mechanism.
Newly synthesized transmembrane and secretory proteins in eukaryotic cells traverse a complex route to their final destinations. The biosynthetic pathway begins when newly synthesized proteins are translocated into the endoplasmic reticulum and ends at the trans-Golgi network (TGN),1 a Golgi-associated tubular network where proteins are sorted into distinct membranous carriers. The TGN serves as a sorting station to segregate proteins destined for endosomes, lysosomes, and the plasma membrane. To add to this complexity, proteins destined for the cell surface can be sorted into distinct types of transport carriers. This additional level of sorting is most obvious in polarized epithelial cells where the plasma membrane is differentiated into discrete apical and basolateral domains. In these cells, delivery of newly synthesized apically and basolaterally destined proteins from the TGN to the cell surface is critical for the maintenance of the different protein and lipid compositions at either cell surface domain (for reviews, see Refs. 1 and 2). Interestingly, the distinct sorting of "apical" and "basolateral" proteins into separate carriers that bud from the TGN is recapitulated in nonpolarized epithelial cells as well as in several non-differentiated cell types including fibroblasts and Vero cells (37). Nonpolarized cells thus provide a useful model in which to investigate the regulation of TGN sorting and export of different classes of proteins, including markers of the apical and basolateral biosynthetic pathways.
While considerable research has been directed toward dissecting the signals on cargo molecules that mediate their polarized delivery, the mechanisms by which these signals are interpreted and the machinery involved in sorting apical and basolateral proteins remain largely unknown. Basolateral targeting signals are generally localized to discrete amino acid sequences in the cytoplasmic domains of proteins. Cytosolic adaptor protein (AP) complexes recognize these motifs and link the cargo to a coat protein such as clathrin (8). Various AP complexes have been implicated in targeting proteins to the basolateral but not the apical surface (911). However, TGN-derived vesicles containing basolaterally destined proteins are not clathrin-coated (12). A role for coatomer in basolateral protein export has also been suggested (13); however, a recent report has questioned the requirement for any coats in the formation of TGN-derived basolateral carriers enriched in basolateral proteins (14). In contrast to basolateral proteins, sorting of apically targeted proteins generally depends on motifs within the luminal or transmembrane domains, although some examples of cytoplasmically disposed apical targeting signals have also been described (15, 16). N- and O-linked carbohydrates are required for apical targeting of a subset of proteins (1721). The association of some proteins with sphingolipid-enriched microdomains or rafts in the TGN has also been proposed to direct their apical delivery (22). Influenza hemagglutinin (HA) has been used extensively as a marker for the apical pathway in polarized cells. Sorting information resides within the transmembrane domain of HA, although no transferable amino acid sequence has been identified (23, 24). HA is efficiently incorporated into lipid rafts, although the correlation between lipid raft association and polarity is unclear (2325). While little is known about how this protein is packaged into apically destined vesicles at the TGN, cell surface delivery of HA is disrupted by expression of influenza M2, an acid-activated proton channel that elevates the pH of acidified intracellular compartments, including the TGN (2630). To begin to identify the cytosolic requirements for the formation of apically destined vesicles from the TGN, we reconstituted ATP- and cytosol-dependent TGN export of prestaged HA in perforated HeLa cells. Our data suggest that this transport assay faithfully recapitulated in vivo requirements for efficient HA release from the TGN. Moreover we found that ADP-ribosylation factor 1 (ARF1), a small GTP-binding protein required for recruitment of adaptor and coat proteins to the Golgi complex and the TGN, was not required for efficient HA release. Additionally HA release under ARF-depleted conditions remained sensitive to selective inhibitors that disrupt HA export in the presence of ARF1, suggesting that ARF depletion does not cause rerouting of HA into alternative transport carriers. Together our data suggest that packaging and export of apical proteins does not require the assembly of known coat protein complexes.
AntibodiesMonoclonal antibody Fc125 directed against influenza HA was a gift from Dr. T Braciale (University of Virginia, Charlottesville, VA). Monoclonal antibody mAD against -COP was from Sigma. Anti-ARF monoclonal antibody 1D9 was from AbCam. Polyclonal antibody against the AP-1 -subunit was a gift from Dr. Linton Traub (University of Pittsburgh, Pittsburgh, PA). Anti-giantin and -GM130 were gifts from Dr. Adam Linstedt (Carnegie Mellon University, Pittsburgh, PA). Anti-TGN46 antibody (AHP500) was obtained from Serotec. Anti-green fluorescent protein polyclonal antibody was obtained from Molecular Probes.
Cell Lines, Adenoviral Infection, and TransfectionHeLa cells were cultured in Dulbecco's modified Eagle's medium (Invitrogen) supplemented with 10% fetal bovine serum. The generation and propagation of replication-defective recombinant adenoviruses encoding tetracycline-repressible influenza HA Japan serotype, influenza M2 Rostock serotype, a control virus (encoding influenza M2 in the reverse orientation), and constitutively expressed tetracycline transactivator are described in Ref. 31. Cells were infected using replication-defective recombinant adenoviruses (multiplicities of infection of 50 for HA, 200 for M2 or M2 in the reverse orientation, and 100 for tetracycline transactivator) as described previously (27, 31), and experiments were performed the following day. cDNA constructs encoding the amino terminus of human
Preparation of CytosolRabbit liver cytosol was prepared from one fresh rabbit liver using the protocol described for rat liver cytosol (32). Rat brain cytosol was prepared from 50 frozen unstripped rat brains (Pelfreeze Biologicals) as described previously (33). ARF-depleted cytosol was prepared from rat brain cytosol using a procedure described previously (34). The resultant cytosols ranged in concentration from
Immunofluorescence and Immunogold Electron MicroscopyIndirect immunofluorescence detection of giantin, AP-1, ARF1, and Protein Staging in the TGNHeLa cells infected with replication-defective recombinant adenoviruses were incubated for 30 min at 37 °C (unless otherwise stated) in bicarbonate-free, cysteine-free, methionine-free Dulbecco's modified Eagle's medium and then metabolically radiolabeled for 10 min in the same medium supplemented with 50 µCi/ml Tran35S Label (MP Biomedicals). The medium was then replaced with cold bicarbonate-free minimal essential medium, and the cells were incubated at 19 °C for 2 h to stage newly synthesized proteins in the TGN. The dishes were then transferred to an ice-cold aluminum plate, and the cells were perforated as described below prior to reconstitution of protein export. Reconstitution of Vesicle Release from Perforated CellsProtein export from the TGN was reconstituted using a modification of the assays described in Refs. 37 and 38. HeLa cells in 10-cm dishes were incubated for 10 min on ice in 10 mM HEPES, pH 7.2, 15 mM KCl, and the cells were then scraped into break buffer (BB; 50 mM HEPES, pH 7.2, 90 mM KCl) using a rubber policeman. The cells were then transferred to a 15-ml conical tube, and the buffer was adjusted to 500 mM KCl by addition of an equal volume of 50 mM HEPES, pH 7.2, 1 M KCl. The suspension was centrifuged at 800 x g in a Beckman GS-6R centrifuge, and the cell pellet was washed with BB and then resuspended in GGA buffer (25 mM HEPES, pH 7.4, 38 mM potassium glutamate, 38 mM potassium aspartate, 38 mM potassium gluconate, 2.5 mM MgCl2, 2 mM EGTA free acid, 1 mM dithiothreitol). During the perforation procedure, Eppendorf tubes were preloaded with GGA buffer with or without an ATP-regenerating system (1 mM ATP, 8 mM creatine phosphate, 50 µg/ml creatine phosphokinase (all based on final concentrations in a total assay volume of 50 µl)), cytosol (2 mg/ml final concentration), and other reagents as described in individual experiments in a final volume of 25 µl. Aliquots of the perforated cell suspension (25 µl) were distributed into these tubes, and the samples were incubated at 37 °C for 1 h unless otherwise specified and then centrifuged in a tabletop microcentrifuge at 12,000 rpm for 2 min to pellet the cells. The supernatant (containing released vesicles) and pellet (cells) were collected separately. HA was immunoprecipitated from radioactive samples and quantitated by PhosphorImager analysis. Export of endogenous proteins from non-radiolabeled cells was analyzed by immunoblotting. Western blots were quantitated after densitometric scanning using QuantityOne software. Data were analyzed by Student's t test using SigmaStat software (Systat) unless otherwise indicated. p < 0.05 was considered to be statistically significant. Protease Protection AssaySupernatants from perforated cells reconstituted with an ATP-regenerating system and cytosol were incubated with 100 µg/ml trypsin (bovine pancreas, treated with L-1-tosylamido-2-phenylethyl chloromethyl ketone, Sigma) in GGA buffer on ice in the presence or absence of 0.05% Triton X-100. After 10 min, soybean trypsin inhibitor was added to a final concentration of 200 µg/ml. The samples were then centrifuged at 100,000 x g for 30 min in a Sorvall RC M120EX centrifuge. Pelleted vesicles were solubilized, and HA was immunoprecipitated from the supernatants as described in Ref. 26. The samples were run on 12% SDS-polyacrylamide gels, dried, and quantified as described above.
Reconstitution of HA Release from Perforated CellsAs a prelude to identifying cellular factors that regulate the TGN sorting and export of apical proteins, we tested the ability of several previously described in vitro transport assays to reconstitute the release of TGN-staged HA in epithelial cells. Our goal was to develop an assay that was reproducible, that was relatively robust, and that recapitulated in vivo sorting in the TGN. Although we could reconstitute pH-sensitive HA release from mechanically perforated polarized MDCK cells (27), vesicle release in this assay was inefficient, and the degree of perforation obtained was inconsistent. Reconstitution of HA release from isolated Golgi preparations purified from polarized MDCK cells was both efficient and reproducible but did not recapitulate physiological properties of sorting observed in vivo.2 However, we found that release of TGN-staged HA from hypo-osmotically swelled, perforated HeLa cells was relatively robust, reproducible, and sensitive to conditions that inhibit HA transport in vivo. HeLa cells expressing HA were metabolically radiolabeled for 10 min, and newly synthesized HA was staged in the TGN by incubation for 2 h at 19 °C. Subsequently the cells were perforated by swelling and scraping, and vesicle release was reconstituted in the presence or absence of an ATP-regenerating system and cytosol. As shown in Fig. 1A, release of HA was robust only when both ATP and cytosol were present. The efficiency of HA release was dependent on the concentration of cytosol with maximal release observed at 2 mg/ml (Fig. 2A). Moreover, using this assay, we observed similar kinetics of HA release when transport was reconstituted using either rat brain or rabbit liver cytosol (Fig. 2B).
To confirm that HA release in this assay was not due to nonselective fragmentation of the Golgi/TGN upon reconstitution, we examined the release of Golgi residents in this assay. Reconstitution of vesicle release did not dislodge the Golgi-associated peripheral membrane protein GM130 (Fig. 1A). In addition, we did not observe measurable release of p58-YFP or the trans-Golgi marker GalT-YFP. However, release of TGN46, a TGN protein that constitutively cycles via the TGN and the basolateral cell surface of polarized MDCK cells (40), was very efficiently reconstituted in the presence of ATP and cytosol (Fig. 1A). Efficient release of this protein from purified rat liver Golgi membranes has been reported previously by another group (41). The release of TGN46 in our assay likely represents release of this protein from the TGN as opposed to the budding of endocytic vesicles from the cell surface because 1) this protein localizes to the TGN in HeLa cells at steady state and after incubation at 19 °C and 2) the small population of TGN46 that can be biotinylated at the plasma membrane at steady state was not released into the medium upon cell perforation and reconstitution.2 We also used immunofluorescence microscopy to examine the effect of perforation and reconstitution on the morphology and localization of the Golgi complex/TGN. Staining with antibodies directed against the Golgi-resident protein giantin and the TGN-localized AP-1 complex demonstrated that these compartments remain concentrated in the perinuclear region of perforated cells after reconstitution, similar to their localization in intact cells (Fig. 1B). A prediction of our assay is that TGN-staged HA should be released in intact membrane-bound carriers. To test this, we first combined immunoelectron microscopy with negative staining to visualize the membranes of released carriers containing HA. Released transport carriers were fixed and processed for visualization of HA-positive structures. Anti-HA antibodies localized to membrane-limited, spherical vesicles with an average diameter of 86 ± 13 nm (mean ± S.D., n = 47; Fig. 3A). To examine the topology of released HA, we examined whether the protease-sensitive luminal domain was protected from trypsin cleavage. Supernatants from a transport reconstitution experiment were incubated with trypsin in the presence or absence of Triton X-100 and then centrifuged at high speed to pellet membrane-bound vesicles (Fig. 3B). In the absence of detergent, cleavage of HA was virtually undetectable, and nearly all of the protein was recovered intact in the pelleted vesicle fraction. By contrast, when Triton X-100 was included, HA was efficiently cleaved and was recovered primarily in the supernatant.
Nucleotide Dependence of HA ReleaseA number of GTPases have been implicated in the delivery of HA from the TGN to the plasma membrane, including ARF1 and Gs (42, 43). To determine whether there is a requirement for GTP or GTP hydrolysis in HA release, we tested the effect of poorly hydrolyzable GTP analogs in our assay (44). Inclusion of GTP S in the reconstitution reaction decreased HA release in a dose-dependent manner with complete inhibition of ATP-dependent release observed at 100 µM concentration (Fig. 4A). However, the more poorly hydrolyzable GTP analog GMP-PNP did not inhibit HA release even at high concentration (Fig. 4C). Neither GTP S nor GMP-PNP affected TGN46 release at 100 µM concentration, indicating that GTP hydrolysis is not required for efficient release of TGN46 from the TGN (Fig. 4, B and D).
HA Release Is Sensitive to in Vivo Perturbants of Biosynthetic TrafficWe have observed previously that disruption of TGN pH by expression of the acid-activated ion channel influenza M2 selectively inhibits efficient release of apical proteins including HA from the TGN in intact MDCK and HeLa cells (26, 27). To examine whether this requirement for acidic TGN luminal pH is preserved in our perforated cell assay system, we examined HA release in HeLa cells co-infected with adenovirus encoding either M2 or as a control M2 in the reverse orientation. After radiolabeling and incubation at 19 °C, cells were perforated, and transport was reconstituted. One set of M2-containing samples was reconstituted in the presence of the M2 channel blocker amantadine. HA release in perforated cells expressing active M2 was decreased by roughly 50% relative to HA release observed in control cells (Fig. 5A). Moreover the effect of M2 on HA release was abrogated by inclusion of amantadine in the reconstitution mixture. The effect of M2 on HA release was reproducible and statistically significant (p < 0.001 versus control cells and p = 0.04 versus M2-expressing cells reconstituted in the presence of amantadine by paired t test analysis of nine independent experiments). By contrast, release of the basolaterally targeted protein TGN46 was unaffected by expression of active M2 (Fig. 5B). In the experiment shown, a slight inhibition was observed in the presence of amantadine; however, this was neither statistically significant nor reproducible.
ARF-independent Release of HAA role for ARF1 has been suggested in numerous transport steps through and from the Golgi complex, but whether it functions in the release of apical proteins from the TGN is not known. Although ARF1 is dissociated from the TGN in intact MDCK cells by brefeldin A, this drug does not function in vitro (45). Therefore, to address the role of ARF1 in HA release in vitro, we used anion-exchange chromatography to deplete rat brain cytosol of ARF1. Immunoblotting of the resulting cytosol routinely demonstrated removal of >87% of ARF1 with no loss of -COP (Fig. 6A).
-COP is readily recruited to the Golgi complex of digitonin-permeabilized cells incubated with exogenous cytosol in the presence of ARF1 and GTP S. Whereas we observed robust binding of -COP to the Golgi complex in permeabilized cells incubated with control cytosol, only background levels of binding were observed in cells incubated with ARF-depleted cytosol (Fig. 6B). Furthermore recruitment of clathrin to the Golgi complex/TGN was also decreased by depletion of ARF1 from cytosol, confirming that recruitment of these coats in this system is still dependent on ARF1 function.2
We next examined the effect of ARF-depleted cytosol on the release of endogenous proteins in HeLa cells in our in vitro assay. Uninfected HeLa cells were radiolabeled for 15 min and then incubated in chase medium at 20 °C for 2 h to accumulate newly synthesized proteins in the TGN. After perforation, vesicle release was reconstituted using ATP and control or ARF-depleted cytosol. Released vesicles were centrifuged in high salt-containing buffer to remove peripheral proteins whose association with membranes might be ARF-dependent, and the protein profile in the pelleted vesicles was analyzed by SDS-PAGE and densitometry (Fig. 6C). While the overall profile of proteins released in the presence of control and ARF-depleted cytosol was similar, we reproducibly observed a decrease in the release of a
We next examined the effect of ARF-depleted cytosol on release of HA and TGN46 from perforated cells. By contrast with p58, whose release was inhibited by
Others have shown that when ARF is depleted from cytosol, release of proteins can still occur in vitro but is no longer sensitive to inhibition by poorly hydrolyzable GTP analogs (34, 45). We therefore tested whether HA release in the presence of ARF-depleted cytosol was affected by GTP
Identifying the molecular requirements for specific steps in protein trafficking has proven difficult due to the numerous compartments within the biosynthetic pathway. To circumvent this issue, many studies have utilized in vitro assays to reconstitute a specific step in membrane transport. Here we used a perforated cell assay to examine the requirements for TGN export of influenza hemagglutinin, a raft-associated protein that has apical sorting information when expressed in polarized epithelial cells. Release of TGN-staged HA from perforated, salt-washed cells was dependent on addition of an ATP-regenerating system and cytosol and was not due to nonspecific fragmentation of the Golgi complex as no release of peripheral or integral Golgi proteins was observed. HA was released in the correct topology in roughly spherical intact transport carriers with an average diameter of 86 ± 13 nm. Importantly, the assay allows rapid removal of cytosolic components prior to reconstitution and appears to preserve physiological pH gradients within organelles as expression of the acid-activated proton channel influenza M2 inhibited the release of HA in our assay. By contrast, while we were also able to efficiently reconstitute HA release from TGN-containing Golgi membranes isolated by subcellular fractionation, release in this assay was insensitive to M2 activity.2 Interestingly, HA release from perforated cells was profoundly inhibited by GTP S but was unaffected by depletion of clathrin2 or ARF1, a GTPase that regulates the binding of all known coats and adaptor proteins to the TGN. Thus, the formation of HA-containing transport carriers appears to proceed via a novel mechanism.
We also reconstituted ATP- and cytosol-dependent release of TGN46, a protein localized to the TGN at steady state but that cycles constitutively through the basolateral cell surface of polarized epithelial cells (40, 46). The release of TGN46 in our assay system was remarkably robust (typically
In contrast to the release of HA, export of TGN46 from the TGN was insensitive to expression of active influenza M2. TGN-staged VSV G release was also insensitive to M2 in our assay system.4 These results are consistent with our previously published studies demonstrating a selective effect of M2 expression on the TGN export of apically sorted proteins in polarized MDCK cells (27) and add further support to the hypothesis that segregation of apical and basolateral proteins into distinct transport carriers also occurs in nonpolarized cells.
Cytosol prepared from a number of sources, including rat brain, rabbit liver, and MDCK cells, was able to support HA release with similar dose dependence. The ability to use various cytosol sources allows the potential modification of cytosolic components by using either genetically altered animals or modified cells. The kinetics of HA release could be monitored in our assay, and similar rates of HA release were observed when TGN export was reconstituted using either rat brain or rabbit liver cytosol. Previous studies have implicated specific cytosolic proteins, including members of the annexin family (49, 50), a heterotrimeric Gs protein (42), dynamin (51), and Cdc42 (52) in the TGN export of apical proteins. The ability to measure the rate of protein release from the TGN should prove useful in experiments designed to determine the order in which different cytoplasmic components function in the formation of HA-containing transport carriers.
Guanine nucleotide analogs have been used extensively to mimic GTP in systems where the nucleotide would be rapidly hydrolyzed. We found that GTP
Morphology of TGN-derived Transport CarriersAlthough numerous adaptor and coat proteins are known to bind TGN membranes, the requirement for these proteins in polarized biosynthetic transport remains unclear. Simon et al. (13, 55) demonstrated that release of sialylated VSV G from Golgi-enriched MDCK membranes requires ARF and occurs via COPI-coated vesicles, whereas another group has suggested a requirement for AP-3 in the TGN export of VSV G (10). Vesicular and tubular structures coated with p230, a peripheral protein of unknown function, have also been observed emanating from the TGN; however, whether biosynthetic cargo molecules are enriched in these carriers is not known (56). G How the sorting and TGN export of proteins that are targeted apically in polarized cells is regulated is no better understood. Apical targeting signals on many proteins, including HA, are localized to the transmembrane or luminal domains of these molecules and are thus unavailable to bind directly to cytoplasmic adaptors (24, 58). Thus, it is not surprising that the regulation of apically destined protein export would be distinct from basolateral transport as we observed. Indeed the molecular requirements for fusion of TGN-derived carriers with the apical plasma membrane of MDCK cells are known to be distinct from those involved in basolateral delivery (59). Several studies have used live cell imaging to characterize Golgi export of fluorescent apical marker proteins in both nonpolarized and polarized cells. Kreitzer et al. (51) described a mixture of vesicular and very long tubular carriers enriched in a non-raft-associated apical cargo molecule that emanated from the TGN of MDCK cells and fused with the plasma membrane. Other groups have reported that a fluorescent apically targeted glycosylphosphatidylinositol-anchored (raft-associated) protein is transported from the TGN primarily in "small" spherical carriers in both nonpolarized and polarized cells compared with transport carriers enriched in basolateral cargo (5, 7). In contrast, Jacob and Naim (6) described the release of large globular structures from the TGN that contained both raft-associated and raft-independent apically targeted cargoes; these large structures resolved into distinct carriers later during transport. Most recently, Polishchuk et al. (60) reported that raft-associated glycosylphosphatidylinositol-anchored proteins are sorted from the TGN to the basolateral membrane of MDCK cells in the same carriers that contain VSV G and then selectively transcytosed to the apical membrane. In contrast to the wide variety of morphologies observed in live cells, the size and structure of transport carriers we isolated upon in vitro reconstitution of HA export was relatively uniform (86 ± 13-nm diameter). Our data are very consistent with a previous study by Wandinger-Ness et al. (61), who reported a diameter of 78 ± 15 nm for TGN-derived, HA-containing vesicles immunoisolated from perforated MDCK cells. Although the vesicles we identified were devoid of a noticeable coat, they were comparable in size to COPI- (50 ± 16-nm diameter (62)), COPII- (70 ± 20-nm diameter (63)), and clathrin-coated (95.9 ± 10.5-nm diameter (64)) vesicles. It is possible that tubule formation is inefficient in our in vitro reconstitution assay; alternatively large globular or tubular transport carriers may not be efficiently released or separated from perforated cells.
HA Export from the TGN Is ARF1-independentARF1 is required for the binding of all adaptor and coat proteins that have been localized to the TGN. As such, we were somewhat surprised to find no requirement for ARF1 in the release of either HA or TGN46. Depletion of ARF1 from the cytosol used to reconstitute TGN export inhibited the association of coatomer and clathrin with the Golgi complex, but an effect on the release of only a single protein could be detected. Happe and Weidman (34) have previously observed that intra-Golgi transport was also efficiently reconstituted in the absence of ARF1 but was no longer sensitive to inhibition by GTP Previous studies have suggested a role for ARF1 in apical biosynthetic transport. Brefeldin A, a drug that inhibits ARF1 function, has been reported to cause rerouting of apical proteins, including HA, to the basolateral cell surface of MDCK cells (6567). While the drug has no effect on the morphology of the Golgi complex of MDCK cells, brefeldin A treatment resulted in the redistribution of both HA and a chimeric protein containing TGN38-derived sorting information into a network of tubules emanating from the TGN (67). However, cell surface delivery of basolateral markers in MDCK cells was unaffected even at high concentrations of brefeldin A (65, 66). These results are most consistent with a role for ARF1 in sorting of apical cargo as opposed to the formation of apically destined vesicles. To test this idea, we asked whether TGN export of HA upon reconstitution with ARF-depleted cytosol was sensitive to inhibition by influenza M2. We found that HA release in ARF-depleted cytosol was still inhibited by expression of active M2. This suggests that the fidelity of HA sorting into transport carriers devoid of basolaterally destined proteins remained intact in the absence of ARF1 function. Although we found no evidence for a direct role for ARF1 in HA export from the TGN, it is possible that ARF1 is important for other steps in TGN-to-cell surface transport. For example, ARF1 could mediate retrograde trafficking of proteins whose function is required for sorting. It has been hypothesized that lectin-like sorting receptors may be responsible for recognition of glycan sorting signals on some apical proteins in the TGN (20). An alternative hypothesis is that ARF1 mediates the recruitment of molecular motors that drive surface delivery of TGN-derived vesicles. ARF1 has recently been implicated in recruitment of the Arp2/3 complex to the Golgi (68, 69). In conjunction with N-WASP, the Arp2/3 complex can drive actin polymerization that propels HA-containing transport carriers from the Golgi region to the cell periphery (70). Thus ARF1 may function in post-Golgi delivery of newly synthesized apical proteins to the plasma membrane in vivo, but this function may not be observed in our in vitro assay. In summary, we used an in vitro reconstitution assay that faithfully preserves in vivo requirements for polarized protein sorting to demonstrate that the formation of TGN-derived transport carriers enriched in a raft-associated apical protein requires cytosolic factors but occurs independently of ARF1 function. The existence of apical sorting mechanisms independent of ARF1 at the TGN is a novel finding. Future experiments will be directed toward identifying the cytosolic machinery involved in this transport step. In addition, it will be important to determine whether similar factors are involved in TGN release of raft-independent apical cargo molecules that contain different sorting information.
* This project was supported by National Institutes of Health Grant R01 DK54407 (to O. A. W). The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.
1 The abbreviations used are: TGN, trans-Golgi network; ARF, ADP-ribosylation factor; AP, adaptor protein; COP, coatomer; GTP
2 M. A. Ellis and O. A. Weisz, unpublished observations.
3 M. A. Ellis, M. T. Miedel, and O. A. Weisz, unpublished observation.
4 M. T. Miedel and O. A. Weisz, unpublished observation.
We thank W. Giovanni Ruiz, Ana Bursick, Donna Beer Stolz, and Simon Watkins for assistance with transmissionelectron microscopy and Linton Traub, Gerard Apodaca, Adam Linstedt, Jennifer Lippincott-Schwartz, Peggy Weidman, and Rebecca Hughey for reagents and numerous helpful suggestions.
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