INTRODUCTION

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Human T-cell leukemia virus type 1 (HTLV-1) is the etiologic agent of adult T-cell leukemia/lymphoma (ATLL) (16, 55, 37), as well as the neurologic disorder tropical spastic paraparesis/HTLV-1-associated myelopathy (TSP-HAM) (14, 33, 42). HTLV-1 induces a lifelong chronic infection, which may result in ATLL in 1 to 5% of carriers 20 to 30 years after infection. Despite a vigorous host immune response, HTLV-1 persists in the infected host, suggesting that the virus may have developed strategies to evade the host's immune response, as is the case with other chronic viruses (36, 49).

The major histocompatibility complex class I (MHC-I) molecules, which are essential for presentation of foreign peptides to the host cytotoxic T lymphocytes (CTL), are targets of many pathogens, including viruses (36, 49). CTL recognize virus-infected cells through the specific interaction of their T-cell receptor with an MHC-I molecule presenting a viral peptide. The MHC-I complex consists of a heavy chain (Hc) containing the peptide binding site and ₂-microglobulin, which assemble very rapidly in the lumen of the endoplasmic reticulum (ER). Peptides, generated by the proteasome in the cytoplasm, are translocated by TAP (transporter associated with antigen processing) into the ER where they assemble in ternary complexes and are transported to the cell surface for presentation to CTL (54). Interference with the assembly and/or trafficking of the MHC-I complex can contribute to the persistence of a virus, although natural killer (NK) cells can recognize and lyse cells that lack MHC-I antigens (19).

Several viruses that induce chronic infections encode proteins that target or modulate the host's immune system (36, 49). Adenovirus was the first virus shown to affect antigen presentation; the E3/19K adenovirus protein binds to MHC-I in the ER and prevents its transport to the cell surface (49). In addition, the E3/19K protein binds TAP and prevents TAP-class I association, thereby interfering with peptide loading (3). Human cytomegalovirus (HCMV) encodes multiple proteins that target MHC-I synthesis, peptide loading, and transport. Murine CMV glycoprotein, gp34, also interacts with the Hc-₂-microglobulin complex in the ER and has been recently shown to target MHC-I for degradation in the lysosomes (49). ICP47, a protein encoded by herpes simplex virus, inhibits the TAP transporter (36, 49). More recently, it was demonstrated that the K3 and K5 proteins encoded by Kaposi's sarcoma-associated herpesvirus downregulated MHC-I from the cell surface (17).

The human immunodeficiency virus (HIV) or simian deficiency virus (SIV) Nef protein downregulates both CD4 and MHC-I expression at the cell surface by interacting with the intracellular sorting machinery of the cell (1, 6, 27, 46). Binding of Nef to a vacuolar ATPase results in the internalization and degradation of CD4 (26). Nef also misroutes MHC-I complexes to the clathrin-coated vesicles (25, 46).

In the case of HTLV-1, alterations in HLA expression on the cell surface have been demonstrated in peripheral mononuclear lymphocytes isolated from patients with adult T-cell leukemia, as well as in HTLV-1-infected cell lines (28, 47, 51). A loss of HLA antigens on the surface of cells from asymptomatic carriers and a gain in their cell surface expression after the development of ATLL has also been suggested (47). Ectopically expressed Tax, the viral transactivator, has also been shown to increase MHC-I expression on the surface of transfected glial cells (44), an event that could contribute to escape from NK cells (51).

The x-I open reading frame of HTLV-1 encodes a protein termed p12^I that exhibits weak oncogenic activity, shares amino acid similarities with the bovine papillomavirus type 1 E5 oncoprotein (13), and binds to the interleukin-2 receptor (IL-2R)  and _c chains (30). Although p12^I expression has been difficult to demonstrate in HTLV-1-infected cells, indirect evidence suggests its importance. The spliced mRNA encoding p12^I has been detected in vitro and ex vivo HTLV-1-infected T-cell lines and macrophages (5, 21, 22). Sera from rabbits experimentally infected with HTLV-1, or sera from humans infected with HTLV-1, recognize the ORF-1 protein product (9). Moreover, a CTL response to the ORF-1 products can be detected in HTLV-1-infected individuals (35). Two natural variants of the p12^I protein have been identified; one carries a lysine at position 88 and is found mainly in HTLV-1 strains from TSP-HAM patients; the second carries an arginine at position 88 and is found in HTLV-1 strains from all ATLL patients and healthy carriers studied (50). The p12^IR88 protein has a much greater stability compared to the p12^IK88 protein, which is ubiquitinated and rapidly degraded by the proteasome (50), suggesting that this sequence variation might be important. The functional relevance of the natural variants of p12^I remains unclear and, while p12^I does not appear necessary for HTLV-1 replication in vitro (10, 41), the appropriate splicing and expression of the ORF-1 mRNA is necessary for the establishment of persistent infection in an in vivo rabbit model (8).

	MATERIALS AND METHODS

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Expression plasmids and antibodies. The pME18S expression vector was obtained from Atsushi Miyajima (DNAX, Palo Alto, Calif.) and contains a hybrid promoter consisting of the simian virus 40 early region promoter and the R region of the HTLV-1 long terminal repeat (LTR). This plasmid was used to express the p12^IK88 and p12^IR88 cDNAs, tagged with the HA1 epitope (23).

DNA transfection and metabolic labeling. One million HeLa-Tat cells were plated in a 10-cm dish and transfected the following day with 10 µg of each plasmid using the calcium phosphate method (15). The total DNA transfected was normalized to 20 µg in each transfection. At 24 h after transfection, cells were incubated for 1 h in medium that lacks methionine and cysteine and was supplemented with 2 mM L-glutamine. Cells were then metabolically labeled for 2 to 3 h with 100 µCi of EXPRES³⁵S³⁵ (NEN Life Sciences, Boston, Mass.) per ml. Cells were washed with 1× phosphate-buffered saline (PBS) and lysed in 1 ml of 1× RIPA buffer (1% deoxycholic acid, 0.1% sodium dodecyl sulfate [SDS], 1% Trition X-100, 0.15 M NaCl, 50 mM Tris-Cl [pH 7.5]) containing 20 µg of aprotinin (Sigma, St. Louis, Mo.) per ml, 20 µg of leupeptin (Roche) per ml, 1 mM AEBSF (ICN, Aurora, Ohio), and 0.5 mM dithiothreitol (DTT; Sigma) and sheared through a 25-gauge needle. Lysates were precleared for 2 h at 4°C with 50 µl of protein A-agarose beads (Roche) and 20 µl of normal rabbit serum. The supernatant was incubated overnight at 4°C with 5 µg of specific antibody. Bound immunocomplexes were extensively washed in cold 1× RIPA buffer and boiled in 2× SDS-loading buffer (Novex, San Diego, Calif.) and -mercaptoethanol. Proteins were analyzed by SDS-polyacrylamide gel electrophoresis (PAGE) on 10 and 15% polyacrylamide gels. Gels were placed for 20 min in Enlightening-Rapid Autography Enhancing solution (NEN Life Sciences), dried under vacuum, and exposed to film.

Lactacystin treatment. HeLa-Tat cells were transfected as described above with the addition of the following: 10 µM lactacystin (Calbiochem, San Diego, Calif.) or as a control, the equivalent volume of dimethyl sulfoxide (DMSO) was added to the starvation medium for 1 h. Cells were then metabolically pulsed for 10 min in labeling medium supplemented with 10 µM lactacystin or DMSO, which was followed by a chase for the indicated time points. All subsequent manipulations were performed as described previously.

Confocal microscopy. The dual-staining immunofluorescence studies were carried out using transfected HeLa-Tat cells. At 30 to 40 h after transfection, cells were analyzed by indirect immunofluorescence after being fixed in paraformaldehyde (3.7%) and permeabilized with Nonidet P-40 (0.1%). AU1-tagged p12^I was detected using AU1 antibody. The plasmid pCMV-Go-GFP was generated by fusing the Golgi targeting sequence of sialyl transferase (34) to the Aequorea victoria green fluorescent protein (GFP) open reading frame (38). Expression was driven by the human CMV promoter and the protein was detected using a rabbit polyclonal serum recognizing GFP (a gift of Markus Neumann, GSF, Munich, Germany). Cells were stained with a mixture of rabbit GFP sera and mouse AU1 antibody, followed by a mixture of Texas red-conjugated anti-mouse antibody to detect p12^I and fluorescein isothiocyanate (FITC)-conjugated anti-rabbit antibody to detect Go-GFP. The sample was then analyzed by laser scanning confocal microscopy using excitation wavelengths of 488 and 543 nm. The ER compartment was visualized using a rabbit polyclonal antiserum specific for calreticulin (Affinity Bioreagents, Inc.) and was visualized with a Texas red-conjugated secondary antibody at an excitation wavelength of 568 nm. For this study, p12^I-AU1 was visualized with an FITC-conjugated secondary antibody at an excitation wavelength of 488 nm. FITC- and Texas red-conjugated secondary antibodies were purchased from Sigma and Jackson Immunoresearch Laboratories (West Grove, Pa.), respectively. Laser scanning confocal microscopy was performed using a Leica TCS-SP system equipped with Argon and helium-neon laser sources using a ×60 objective (see Fig. 5A to C) or an Olympus system equipped with an argon-krypton laser source using a ×60 objective (Fig. 5D to F).

Pseudotype virus production and concentration. 293T cells were seeded at 2 × 10⁶ in a 10-cm dish and transfected the following day with VSV-G (2 µg), CMVHIV (4 µg), and HR'CMV-Luc or HR'CMV p12^I (4 µg) using the Effectene reagent kit (Quiagen) according to the manufacturer's instructions. Supernatant from 20 dishes was collected every 12 h from 24 to 72 h, cleared of cellular debris by centrifugation at 8,000 × g for 10 min at room temperature, filtered (0.45 µm [pore size]), and stored at 80°C. Pseudotype viruses were pelleted by ultracentrifugation at 50,000 × g (28,000 rpm using an SW41 rotor) for 1 h and 45 min at 4°C. Virus was resuspended in PBS for 4 h on ice, collected, aliquoted, and stored at 80°C. HIV GAG p24 was measured using an antigen capture assay, and infections were performed using comparable amounts of virus particles. Infectivity and proper expression was further verified by immunofluorescence.

Flow cytometric analysis of infected Jurkat cells. Jurkat cells were infected with an equivalent concentration of pseudotyped virus carrying either p12^I or the luciferase genes in RPMI 1640-2% FCS at 37°C with 5% CO₂. After 4 h, the concentration of FCS was increased to 10%. At days 2, 4, and 5 postinfection, cells were removed, washed in PBS, incubated at 4°C with phycoerythrin (PE)-conjugated CD3 or CD4 antibody (PharMingen, San Diego, Calif.) or with anti-human MHC-I antibody, W6/32 (Sigma), followed by a PE-conjugated secondary antibody (PharMingen). Cells were washed with PBS-1% FCS, fixed in 2% paraformaldehyde, and analyzed on a Becton Dickinson FacScan.

	RESULTS

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p12^I binds to newly synthesized MHC-I-Hc before its association with ₂-microglobulin. The fact that HTLV-1 persists in the host despite the vigorous virus-specific host immune response suggests that this pathogen has developed mechanisms to evade immune recognition. We hypothesize that the p12^I protein of HTLV-1 may affect the MHC-I-Hc-₂-microglobulin complex on the basis of the observation that, like the HIV/SIV Nef protein, which affects class I-restricted antigen presentation (7), p12^I is essential for efficient viral propagation in vivo (8). To investigate whether one or both of the two natural variants of p12^I interact with the MHC-I complex, we performed coimmunoprecipitation assays on lysates of HeLa-Tat cells transfected with plasmids expressing HA1-tagged p12^I cDNA and the porcine MHC-I-Hc cDNA; porcine MHC-I-Hc was used in these initial experiments because of its ease of detection. As expected, the tagged p12^IK88 and its ubiquitinated forms were readily immunoprecipitated with the HA1 antibody, as demonstrated in lanes 1 and 2 of Fig. 1B. Interestingly, the 46-kDa porcine MHC-I-Hc protein coimmunoprecipitated with p12^IK88 (Fig. 1A and B, lane 2), indicating that the two proteins interact with each other. Neither p12^IK88 nor the porcine Hc immunoprecipitated with an isotype-matched negative control immunoglobulin G (IgG) antibody (Fig. 1A and B, lanes 7 to 9). Surprisingly, endogenous ₂-microglobulin did not coimmunoprecipitate with p12^IK88 and MHC-I-Hc. This finding, combined with the observation that p12^I appeared to bind faster-migrating forms of MHC-I-Hc (data not shown), suggested that p12^IK88 may bind to a less-glycosylated form of MHC-I-Hc, perhaps in the ER, before its association with ₂-microglobulin. Since the association of the Hc with ₂-microglobulin occurs quite rapidly, within 4 min after translation (32), it is possible that p12^I competes with ₂-microglobulin for binding to newly synthesized Hc. This hypothesis was further supported by the finding that the PT85A antibody, which mainly recognizes the Hc-₂-microglobulin complex, readily precipitated both the MHC-I-Hc and the ₂-microglobulin but did not coprecipitate p12^IK88 (Fig. 1B, lane 5). In parallel experiments, the other variant of p12^I, p12^IR88, also was demonstrated to bind to the free MHC-I-Hc (data not shown).

View larger version (41K): [in this window] [in a new window]   FIG. 1.   The HTLV-1 p12I protein binds to the free MHC-I-Hc but not to the MHC-I-Hc-2-microglobulin complex. Radioimmunoprecipitation was performed on lysates of transfected HeLa-Tat cells with HA1, PT85A, or isotype-matched IgG antibodies. Lysates were analyzed on 10% (A) and 15% (B) acrylamide gels. Arrows indicate the expression of p12IK88 (lanes 1 and 2) and MHC-I-Hc and 2-microglobulin (lanes 5 and 6) and the coimmunoprecipitation of free MHC I-Hc and p12IK88 with the HA1 antibody (lane 2). Ubiquitinated forms of p12IK88 are indicated by arrows on the left. (C) Lysates were also precipitated with an calnexin antibody (10% acrylamide gel).

The p12^I protein interacts with the human MHC-I- A2, -B7, and -Cw4 Hcs. To determine whether p12^I interacts with human MHC-I-Hc, immunoprecipitations were performed on lysates of HeLa-Tat cells cotransfected with plasmids expressing HA1-tagged p12^I and human MHC-I-Hc encoded by either the A2, the B7, or the Cw4 alleles. In these experiments, the p12^IR88 variant was used, since it is more stable and thus easier to detect than p12^IK88 (50). Figure 2A to C shows results obtained for MHC-I-Hc-A2, analyzed using Hc serum, which recognizes free Hc, and the HA1 antibody. The Hc serum precipitated both the p12^I protein and MHC-I-Hc A2 from cells cotransfected with the p12^I- and A2 Hc-expressing plasmids (Fig. 2A and B, lane 8); p12^I was not coprecipitated in transfections carried out in the absence of the A2 Hc plasmid, since the HeLa-Tat cell line does not express the A2 Hc and p12^I does not appear to bind to the endogenous Hc alleles found in HeLa-Tat cells (Fig. 2A and B, lane 6). It was difficult to confirm the identity of A2 Hc in the HA1 (i.e., anti-p12^I) immunoprecipitate due to the presence of a nonspecific comigrating protein (Fig. 2A, lane 4). Control immunoprecipitations carried out with an antibody directed against ₂-microglobulin confirmed that the lysates contained equivalent amounts of the endogenous ₂-microglobulin (Fig. 2C).

View larger version (24K): [in this window] [in a new window]   FIG. 2.   p12I binds to the human A2 and B7 MHC-I-Hc alleles. HeLa-Tat cells were transfected with cDNAs encoding the human A2 and B7 Hc genes in the presence or absence of p12I, metabolically labeled, lysed, and immunoprecipitated with HA1 (A and B, lanes 1 to 4), Hc serum (A and B, lanes 5 to 8), or the W6/32 antibody that recognizes MHC-I A, B, and C complexes (D and E). Lysates were analyzed on 10% (A and D) and 15% (B, C, and E) acrylamide gels. (C) Cell lysates were then immunoprecipitated with antibodies recognizing 2-microglobulin to demonstrate equivalent levels in all transfected cells.

p12^I associates with the immature form of the MHC-I-Hc in a pre-Golgi compartment. The absence of ₂-microglobulin in the Hc-p12^I complex, together with the fact that p12^I binds to a faster-migrating, presumably immature form of the Hc, suggested that this interaction may occur in the ER prior to the association of MHC-I-Hc with ₂-microglobulin. To test this hypothesis, pulse-chase experiments were performed following transfection of the either MHC-I-Hc alone or in the presence of p12^I. The majority of the MHC-I-Hc protein band immunoprecipitated by the PT85A antibody was shifted to higher-molecular-weight forms within the 6-h chase (Fig. 3A, lanes 6 to 8), as expected, which is consistent with the occurrence of glycosylation. In contrast, the size of the MHC-I-Hc complexed to p12^I did not change within 6 h of the chase (Fig. 3A, lane 3) and, interestingly, by 8 h the amount of MHC-I complexed to p12^I was significantly reduced (Fig. 3A, lane 4), suggesting its possible degradation. These data indicate that p12^I binds to the immature, probably incompletely glycosylated forms of the MHC-I-Hc and that this complex may not progress to the Golgi.

View larger version (19K): [in this window] [in a new window]   FIG. 3.   p12I binds to the free Endo-H-sensitive MHC-I-Hc. (A) Transfected HeLa-Tat cells were metabolically labeled, and the decay of the MHC-I-Hc was measured at the time intervals indicated. Cell lysates were immunoprecipitated with either HA1 or PT85A antibodies. (B) The immunoprecipitates were incubated in the absence or presence of Endo-H, with the porcine MHC-I-Hc cleavage product indicated by arrows.

The MHC-I-Hc-12¹ complex is degraded in the proteasome. Misfolded, inappropriately glycosylated, or improperly assembled proteins are removed from the ER using the ER-associated protein degradation (ERAD) pathway and are targeted to the proteasome for degradation (4). In the pulse-chase experiment presented in Fig. 3A, the amount of Hc bound to p12^I at 8 h was greatly diminished. To investigate whether, like misfolded free MHC-I-Hc molecules, the MHC-I-Hc-p12^I complex was targeted for degradation via the proteasome, transfected cells were treated with lactacystin, a specific inhibitor of the proteasome (11). The fate of the Hc-p12^I complex was then analyzed in a pulse-chase experiment. At time zero, the MHC-I-Hc bound to p12^I was detectable only in the presence of the specific proteasome inhibitor (Fig. 4, compare lanes 5 and 7). Similarly, the amount of MHC-I-Hc bound to p12^I was increased in the presence of lactacystin at 45 min (Fig. 4, compare lanes 6 and 8), suggesting that most of the immature MHC-I-Hc bound to p12^I is indeed degraded by the proteasome. Altogether, these results suggest that p12^I interacts with the free Hc in the ER early after Hc synthesis and before its association with the ₂-microglobulin and that most of the MHC-I bound to p12^I is rerouted to the cytosol and targeted to the proteasome for degradation.

View larger version (17K): [in this window] [in a new window]   FIG. 4.   The proteosome inhibitor lactacystin increases the stability of the Hc-p12I complex. Transfected HeLa-Tat cells were metabolically labeled, and the stability of the MHC-I-Hc-p12I complex was assessed by immunoprecipitation with HA1 and PT85A in the presence or absence of lactacystin.

p12^I resides in the ER and/or Golgi compartments. p12^I's association with the free MHC-I suggested that p12^I might reside in the ER and/or Golgi as well. Although previous indirect immunofluorescence studies had demonstrated that p12^I is membrane associated (24), its possible targeting to the membranes of specific organelles had not been investigated. To assess this, HeLa-Tat cells were therefore cotransfected with pCMV-p12^I-AU1 and pCMV-Go-GFP, which expresses a Golgi-targeted GFP (34), and then subjected to immunofluorescence confocal microscopy to detect the two proteins. The G-GFP protein, green signal (Fig. 5A), and p12^I, red signal (Fig. 5B), were found in similar cellular locations, as demonstrated by the almost complete overlap, which generated a yellow signal in the overlay (Fig. 5C), a finding indicative of colocalization in the Golgi.

View larger version (57K): [in this window] [in a new window]   FIG. 5.   Intracellular localization of p12I. HeLa-Tat cells were cotransfected with pCMV-p12I-AU1 and pCMV-Go-GFP, which expresses a Golgi-targeted GFP. (A) The G-GFP protein, detected as a green signal. (B) p12I, detected as a red signal. (C) Overlay of panels A and B. (D and E). Staining of pCMV-p12I-AU1-transfected HeLa-Tat cells with antibodies to calreticulin, an ER-resident protein (red signal) (D), and AU1 (green signal) (E) to detect p12I. (F) Overlay of panels D and E.

p12^I interferes with the intracellular trafficking of MHC-I and decreases the level of MHC-I from the surface of human T cells. Next we investigated whether the association of MHC-I-Hc with p12^I affects the trafficking of the MHC-I molecule to the cell surface. HeLa-Tat cells were therefore transfected with either the porcine MHC-I-Hc alone or together with p12^I. The intracellular distribution of the MHC-I-Hc, as well as the expression of p12^I, was assessed by confocal microscopy. The MHC-I staining was strongest at or near the cell surface in cells that received a control plasmid, whereas in cells cotransfected with p12^I, the level of MHC-I at or near the cell surface was decreased and MHC-I appeared to be distributed predominantly in the cytoplasm or perinuclear area of these cells (Fig. 6A). These results indicate that the interaction of p12^I with MHC-I-Hc in the ER interferes with normal trafficking of MHC-I to the plasma membrane.

View larger version (88K): [in this window] [in a new window]   FIG. 6.   p12I alters the trafficking of MHC-I-Hc to the plasma membrane. (A) HeLa-Tat cells were transfected with a plasmid expressing porcine MHC-I-Hc in the absence or presence of a p12I plasmid and then subjected to immunofluorescence microscopy to examine the effect of p12I on the intracellular distribution and trafficking of the MHC-I-Hc. Control, the MHC I complex is detected at or near the plasma membrane in most cells; p12I cells cotransfected with MHC-I-Hc and p12I have decreased staining at the plasma membrane and increased staining in the cytoplasm, particularly in the perinuclear region. (B) Jurkat T cells were infected with the pseudotyped viruses HR'CMV p12I or HRICMV-Luc, and the surface expression of MHC-I, CD3, and CD4 was examined by flow cytometry over time. There was an approximate 50% reduction in the level of MHC-I on the cell surface in cells expressing p12I at day 5, represented by the heavy lines, while the levels of CD3 and CD4 remain constant throughout. There was no change in MHC-I, CD3, or CD4 levels in control cells, which are represented by the thin lines.

	DISCUSSION

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Several viruses have evolved mechanisms to escape immune recognition by affecting the expression of MHC-I on the cell surface (36, 49). The data presented here suggest that p12^I interferes with the assembly of the free MHC-I-Hc with ₂-microglobulin and affects its trafficking to the cell membrane. It may do so by taking advantage of a pathway termed ERAD, whose purpose is to remove misfolded, inappropriately glycosylated or improperly assembled proteins from the ER (4). Proteins are imported into the ER by co- or posttranslational passage through the ER membrane, a process that is mediated by the translocon, a protein channel consisting of the Sec61p protein complex (40). Evidence suggests that the translocon can also function in reverse, retranslocating proteins to the cytosolic face of the ER membrane, where they lose their N-linked oligosaccharides, undergo ubiquitination, and are targeted to the proteasome for degradation (4). It has been demonstrated that misfolded MHC-I-Hc are targeted for destruction through a pathway involving the Sec61p complex and the proteasome (53). In addition, several other proteins have been demonstrated to be translocated from the ER and degraded in a proteasome-dependent manner: improperly assembled mammalian T-cell receptors, yeast carboxypeptidase Y proteins, the cystic fibrosis transmembrane conductance receptor (CFTR), -antitrypsin, and apolipoprotein B100 (43).

In this study, we demonstrate that p12^I binds to both porcine MHC-I-Hc and the products of the human A2, B7, and Cw4 MHC-I-Hc alleles. This interaction prevents association of MHC-I-Hc with ₂-microglobulin and reroutes newly synthesized MHC-I-Hc's to the cytosol, where they are degraded by the proteasome, in a similar manner to the HCMV proteins, US2 and US11 (52, 53). However, because both US2 and US11 target the MHC-I-Hc-₂-microglobulin complex for proteosomal degradation, whereas p12^I targets the free Hc, the HTLV p12^I protein appears to use a novel mechanism for MHC-I downregulation, whereby this viral protein competes with ₂-microglobulin for binding to the Hc. Studies of US2-expressing cells demonstrated that the protein induces formation of a deglycosylated breakdown intermediate of MHC-I-Hc that associates with the Sec61 complex (53). The Hc-p12^I complex remains in the cis-Golgi compartment, as evidenced by its sensitivity to Endo-H, and most of the complex is retrotranslocated to the cytoplasm and degraded by the proteasome.

Binding of p12^I to MHC-I results in redistribution of MHC-I in the perinuclear area of the cell and consequent decrease in its expression at the plasma membrane. The mechanism of retranslocation of MHC-I bound to p12^I remains to be investigated, as well as the specific fates of the various Hcs encoded by the HLA-A, -B, and -C alleles; the US2 and US11 proteins selectively target HLA-A and -B, but not HLA-C alleles (45), which is also the case with Nef (6, 25). Furthermore, as demonstrated by US2 and US11, binding does not necessarily result in retranslocation and degradation. US2 and US11 are able to bind to "tailless" MHC-I molecules (48), as well as p12^I (data not shown). However, this "tailless" MHC is not retrotranslocated and degraded by US2 and US11 (48). It would be a disadvantage for a virus to downregulate all of the MHC-I at the cell surface, since these cells would become a target for lysis by NK cells (19), and it is interesting to speculate that p12^I may downregulate specific alleles in order to allow the virus to escape detection by the immune system but not to become targets for NK cells. Furthermore, the HTLV-1 Tax protein has been shown to upregulate MHC-I on the cell surface (44); thus, a balance of p12^I and Tax protein levels may allow modulation of MHC-I levels to serve this purpose. Future work will also examine the effect of p12^I on antigen presentation, utilizing the lentiviral vector carrying p12^I to determine whether the decrease in MHC levels at the cell surface induced by p12^I may be sufficient to effect recognition by CTL.

Interestingly, the HTLV-1 p12^I and Nef proteins of HIV and SIV appear to have common features. Nef is dispensible in vitro but is required for in vivo replication and pathogenicity (20), as is p12^I (8). In vitro, p12^I has been shown to bind the 16-kDa subunit of the vacuolar ATPase (13), and Nef has been shown to bind to the catalytic subunit of the same enzyme (26). Since Nef has been shown to affect MHC-I levels at the cell surface (6, 46), here we demonstrate that p12^I interferes with MHC-I-₂-microglobulin assembly and trafficking to the cell membrane using a novel mechanism. In contrast to Nef, however, p12^I interacts with the free MHC-I-Hc, prevents its association with ₂-microglobulin in the ER, and targets the MHC-I-Hc for proteasome degradation, which results in a decrease of MHC-I at the cell surface. Nevertheless, because p12^I also targets the vacuolar ATPase (12, 13), as demonstrated in the case of Nef, it remains to be investigated whether p12^I trafficks to the cell membrane and affects also the endocytosis of MHC-I on the cell surface. Lastly, the two natural alleles of p12^I, one of which (p12^IK88) is ubiquitinated, may differ in their abilities to affect antigen presentation and therefore modulate the host-specific immune response. In this regard, the finding that the ubiquitinated form of p12^I (p12^IK88) is found mainly in TSP-HAM (50), an immune-mediated disease (18, 33), indicates that dissecting the functional consequence of the two natural alleles of p12^I may further our understanding of HTLV-1 pathogenesis.