Abstract |
Human immunodeficiency virus type 1 (HIV-1) viral protein R (Vpr) exerts multiple effects on viral and host cellular activities during infection, including induction of cell cycle G(2) arrest and cell death in both human and the fission yeast Schizosaccharomyces pombe cells. In this study, a mutant derivative of Vpr (F34IVpr), which causes transient G2 arrest with little or no effect of cell killing, was used to study the molecular impact of Vpr on cellular oxidative stress responses in S. pombe. We demonstrated here that F34IVpr triggers low level of complex and atypical oxidative stress responses in comparison with its parental strain SP223 in early (14-h) and late (35-h) log phase cultures. Specifically, F34IVpr production in S. pombe causes significantly elevated levels of reactive oxygen species such as superoxide and peroxides; meanwhile, it also induces decreased levels of glutathione, hydroxyl radical concentrations and specific enzyme activities such as those of antioxidant enzymes including superoxide dismutases, catalase, glutathione peroxidase, glutathione reductase, glucose-6-phosphate dehydrogenase and glutathione transferase. These observations may provide functional insights into the significance of Vpr-induced oxidative stress as part of the multifaceted functions of Vpr, and contribute to the development of future new strategies aimed to reduce the adverse Vpr-mediated effects in HIV-infected patients.
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Authors | Timea Stromájer-Rácz, Zoltán Gazdag, József Belágyi, Csaba Vágvölgyi, Richard Y Zhao, Miklós Pesti |
Journal | Experimental and molecular pathology
(Exp Mol Pathol)
Vol. 88
Issue 1
Pg. 38-44
(Feb 2010)
ISSN: 1096-0945 [Electronic] Netherlands |
PMID | 19837062
(Publication Type: Journal Article)
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Copyright | Copyright 2009 Elsevier Inc. All rights reserved. |
Chemical References |
- Mutant Proteins
- Reactive Oxygen Species
- vpr Gene Products, Human Immunodeficiency Virus
- Hydroxyl Radical
- Oxidoreductases
- Glutathione
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Topics |
- Glutathione
(metabolism)
- HIV-1
(physiology)
- Hydroxyl Radical
(metabolism)
- Mutant Proteins
(metabolism)
- Oxidative Stress
(physiology)
- Oxidoreductases
(metabolism)
- Reactive Oxygen Species
(metabolism)
- Schizosaccharomyces
(growth & development, ultrastructure, virology)
- vpr Gene Products, Human Immunodeficiency Virus
(genetics, metabolism)
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