共 53 条
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.
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页码:583 / 592
页数:10
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