Mechanism of HIV-1 viral protein R-induced apoptosis

被引:60
作者
Muthumani, K [1 ]
Choo, AY [1 ]
Hwang, DS [1 ]
Chattergoon, MA [1 ]
Dayes, NN [1 ]
Zhang, DH [1 ]
Lee, MD [1 ]
Duvvuri, U [1 ]
Weiner, DB [1 ]
机构
[1] Univ Penn, Dept Pathol & Lab Med, Stellar Chance Labs 505, Philadelphia, PA 19104 USA
关键词
HINI-1; Vpr; apoptosis; caspase; mitochondrial membrane potential; NF-kappa B; AIF; cytochrome c;
D O I
10.1016/S0006-291X(03)00631-4
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
The paradigm of HIV-1 infection includes the diminution of CD4(+) T cells, loss of immune function, and eventual progression to AIDS. However, the mechanisms that drive host T cell depletion remain elusive. One HIV protein thought to participate in this destructive cascade is the Vpr gene product. Accordingly, we review the biology of the HIV-1 viral protein R (Vpr) an apoptogenic HIV-1 accessory protein that is packaged into the virus particle. In this review we focus specifically on Vpr's ability to induce host cell apoptosis. Recent evidence suggests that Vpr implements a unique mechanism to drive host cell apoptosis, by directly depolarizing the mitochondria membrane potential. Vpr's attack on the mitochondria results in release of cyrochrome c resulting in activation of the caspase 9 pathway culminating in the activation of caspase 3 and the downstream events of apoptosis. Vpr may interact with the adenine nucleotide translocator (ANT) to prompt this cascade. The role of Vpr-induced apoptosis in HIV pathogenesis is considered. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:583 / 592
页数:10
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