Abstract
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 cytochrome 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.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 583-592 |
| Number of pages | 10 |
| Journal | Biochemical and Biophysical Research Communications |
| Volume | 304 |
| Issue number | 3 |
| DOIs | |
| State | Published - May 9 2003 |
| Externally published | Yes |
Keywords
- AIF
- Apoptosis
- Caspase
- Cytochrome c
- HIV-1 Vpr
- Mitochondrial membrane potential
- NF-κB
ASJC Scopus subject areas
- Biophysics
- Biochemistry
- Molecular Biology
- Cell Biology
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