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HIV-1 Nef increases astrocyte sensitivity towards exogenous hydrogen peroxide

BACKGROUND: HIV-1 infected individuals are under chronic exposure to reactive oxygen species (ROS) considered to be instrumental in the progression of AIDS and the development of HIV-1 associated dementia (HAD). Astrocytes support neuronal function and protect them against cytotoxic substances inclu...

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Detalles Bibliográficos
Autores principales: Masanetz, Sabine, Lehmann, Michael H
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3038946/
https://www.ncbi.nlm.nih.gov/pubmed/21255447
http://dx.doi.org/10.1186/1743-422X-8-35
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author Masanetz, Sabine
Lehmann, Michael H
author_facet Masanetz, Sabine
Lehmann, Michael H
author_sort Masanetz, Sabine
collection PubMed
description BACKGROUND: HIV-1 infected individuals are under chronic exposure to reactive oxygen species (ROS) considered to be instrumental in the progression of AIDS and the development of HIV-1 associated dementia (HAD). Astrocytes support neuronal function and protect them against cytotoxic substances including ROS. The protein HIV-1 Nef, a progression factor in AIDS pathology is abundantly expressed in astrocytes in patients with HAD, and thus may influence its functions. RESULTS: Endogenous expressed HIV-1 Nef leads to increased sensitivity of human astrocytes towards exogenous hydrogen peroxide but not towards TNF-alpha. Cell death of nef-expressing astrocytes exposed to 10 μM hydrogen peroxide for 30 min occurred within 4 h. CONCLUSION: HIV-1 Nef may contribute to neuronal dysfunction and the development of HAD by causing death of astrocytes through decreasing their tolerance for hydrogen peroxide.
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spelling pubmed-30389462011-02-15 HIV-1 Nef increases astrocyte sensitivity towards exogenous hydrogen peroxide Masanetz, Sabine Lehmann, Michael H Virol J Research BACKGROUND: HIV-1 infected individuals are under chronic exposure to reactive oxygen species (ROS) considered to be instrumental in the progression of AIDS and the development of HIV-1 associated dementia (HAD). Astrocytes support neuronal function and protect them against cytotoxic substances including ROS. The protein HIV-1 Nef, a progression factor in AIDS pathology is abundantly expressed in astrocytes in patients with HAD, and thus may influence its functions. RESULTS: Endogenous expressed HIV-1 Nef leads to increased sensitivity of human astrocytes towards exogenous hydrogen peroxide but not towards TNF-alpha. Cell death of nef-expressing astrocytes exposed to 10 μM hydrogen peroxide for 30 min occurred within 4 h. CONCLUSION: HIV-1 Nef may contribute to neuronal dysfunction and the development of HAD by causing death of astrocytes through decreasing their tolerance for hydrogen peroxide. BioMed Central 2011-01-22 /pmc/articles/PMC3038946/ /pubmed/21255447 http://dx.doi.org/10.1186/1743-422X-8-35 Text en Copyright ©2011 Masanetz and Lehmann; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Masanetz, Sabine
Lehmann, Michael H
HIV-1 Nef increases astrocyte sensitivity towards exogenous hydrogen peroxide
title HIV-1 Nef increases astrocyte sensitivity towards exogenous hydrogen peroxide
title_full HIV-1 Nef increases astrocyte sensitivity towards exogenous hydrogen peroxide
title_fullStr HIV-1 Nef increases astrocyte sensitivity towards exogenous hydrogen peroxide
title_full_unstemmed HIV-1 Nef increases astrocyte sensitivity towards exogenous hydrogen peroxide
title_short HIV-1 Nef increases astrocyte sensitivity towards exogenous hydrogen peroxide
title_sort hiv-1 nef increases astrocyte sensitivity towards exogenous hydrogen peroxide
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3038946/
https://www.ncbi.nlm.nih.gov/pubmed/21255447
http://dx.doi.org/10.1186/1743-422X-8-35
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