Apoptosis in AIDS

被引:87
作者
Roshal, M
Zhu, Y
Planelles, V
机构
[1] Univ Rochester, Ctr Canc, Dept Med, Rochester, NY 14642 USA
[2] Univ Rochester, Ctr Canc, Dept Microbiol & Immunol, Rochester, NY 14642 USA
关键词
apoptosis; survival; HIV; vpr; net; tat; env; AIDS;
D O I
10.1023/A:1009636530839
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Infection with the human immunodeficiency virus type 1 (HIV-1) leads to progressive immunodeficiency and onset of opportunistic infections and neoplasms. The loss of immune competence is associated with declines in both the functionality and the number of CD4+ lymphocytes. Multiple mechanisms have been proposed to explain death and dysfunction of CD4+ T-cells. The mechanisms of HIV-1-mediated cell death which are relevant in vivo are unclear at present. However, in vitro explorations on the cytopathic effects of HIV-1 have yielded a wealth of potential triggering events, and signaling and effector pathways leading to apoptosis. The types of pro- and anti-apoptotic stimuli that have been associated with HIV-1 are multiple and often appear overlapping or even contradictory. This review focuses on the various molecular determinants from HIV-1 that play a role in induction of apoptosis in T-lymphocytes. Special attention is devoted to the viral genes, env, nef, tat and vpr, for which a significant body of literature on apotosis-related effects is available.
引用
收藏
页码:103 / 116
页数:14
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