HIV nef-mediated CD4 down-regulation is adaptor protein complex 2 dependent

被引:48
作者
Jin, YJ
Cai, CY
Zhang, XP
Zhang, HT
Hirst, JA
Burakoff, SJ
机构
[1] NYU, Sch Med, Skirball Inst Biomed Res, Lab 5 1, New York, NY 10016 USA
[2] NYU, Sch Med, Dept Med, New York, NY 10016 USA
[3] Rutgers State Univ, Coll Pharm, Dept Pharmaceut, Piscataway, NJ 08854 USA
关键词
D O I
10.4049/jimmunol.175.5.3157
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Nef is a crucial viral protein for HIV to replicate at high titers and in the development of AIDS. One Nef function is down-regulating CD4 from the cell surface, which correlates with Nef-enhanced viral pathogenicity. Nef down-regulates CD4 by linking CD4 to clathrin-coated pits. However, the mechanistic connection between the C-terminal dileucine motif of Nef and the component(s) of the clathrin-coated pits has not been pinpointed. In this report we used two AP-2 complex-specific inhibitors: a dominant negative mutant of Eps15 (Eps15DIII) that binds to the alpha subunit of AP-2 complex and a small interference RNA that is specific for the mu 2 subunit of AP-2 complex. We show that both HIV Nef- and SIV Nef-mediated CD4 down-regulations were profoundly blocked by the synergistic effect of Eps15DIII and RNA interference of AP-2 expression. The results demonstrate that HIV/SIV Nef-mediated CD4 down-regulation is AP-2 dependent. We also show that the PMA-induced CD4 down-regulation was blocked by these two inhibitors. Therefore, PMA-induced CD4 down-regulation is also AP-2 dependent. The results demonstrate that, like the tyrosine sorting motif-dependent endocytosis (for which the transferrin receptor and the epidermal growth factor receptor are the two prototypes), dileucine sorting motif-dependent endocytosis of Nef and CD4 are also AP-2 dependent.
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页码:3157 / 3164
页数:8
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