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SAMHD1 restricts HIV-1 reverse transcription in quiescent CD4(+) T-cells
BACKGROUND: Quiescent CD4(+) T lymphocytes are highly refractory to HIV-1 infection due to a block at reverse transcription. RESULTS: Examination of SAMHD1 expression in peripheral blood lymphocytes shows that SAMHD1 is expressed in both CD4+ and CD8+ T cells at levels comparable to those found in m...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3494655/ https://www.ncbi.nlm.nih.gov/pubmed/23092122 http://dx.doi.org/10.1186/1742-4690-9-87 |
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author | Descours, Benjamin Cribier, Alexandra Chable-Bessia, Christine Ayinde, Diana Rice, Gillian Crow, Yanick Yatim, Ahmad Schwartz, Olivier Laguette, Nadine Benkirane, Monsef |
author_facet | Descours, Benjamin Cribier, Alexandra Chable-Bessia, Christine Ayinde, Diana Rice, Gillian Crow, Yanick Yatim, Ahmad Schwartz, Olivier Laguette, Nadine Benkirane, Monsef |
author_sort | Descours, Benjamin |
collection | PubMed |
description | BACKGROUND: Quiescent CD4(+) T lymphocytes are highly refractory to HIV-1 infection due to a block at reverse transcription. RESULTS: Examination of SAMHD1 expression in peripheral blood lymphocytes shows that SAMHD1 is expressed in both CD4+ and CD8+ T cells at levels comparable to those found in myeloid cells. Treatment of CD4+ T cells with Virus-Like Particles (VLP) containing Vpx results in the loss of SAMHD1 expression that correlates with an increased permissiveness to HIV-1 infection and accumulation of reverse transcribed viral DNA without promoting transcription from the viral LTR. Importantly, CD4(+) T-cells from patients with Aicardi-Goutières Syndrome harboring mutation in the SAMHD1 gene display an increased susceptibility to HIV-1 infection that is not further enhanced by VLP-Vpx-treatment. CONCLUSION: Here, we identified SAMHD1 as the restriction factor preventing efficient viral DNA synthesis in non-cycling resting CD4(+) T-cells. These results highlight the crucial role of SAMHD1 in mediating restriction of HIV-1 infection in quiescent CD4(+) T-cells and could impact our understanding of HIV-1 mediated CD4(+) T-cell depletion and establishment of the viral reservoir, two of the HIV/AIDS hallmarks. |
format | Online Article Text |
id | pubmed-3494655 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-34946552012-11-10 SAMHD1 restricts HIV-1 reverse transcription in quiescent CD4(+) T-cells Descours, Benjamin Cribier, Alexandra Chable-Bessia, Christine Ayinde, Diana Rice, Gillian Crow, Yanick Yatim, Ahmad Schwartz, Olivier Laguette, Nadine Benkirane, Monsef Retrovirology Research BACKGROUND: Quiescent CD4(+) T lymphocytes are highly refractory to HIV-1 infection due to a block at reverse transcription. RESULTS: Examination of SAMHD1 expression in peripheral blood lymphocytes shows that SAMHD1 is expressed in both CD4+ and CD8+ T cells at levels comparable to those found in myeloid cells. Treatment of CD4+ T cells with Virus-Like Particles (VLP) containing Vpx results in the loss of SAMHD1 expression that correlates with an increased permissiveness to HIV-1 infection and accumulation of reverse transcribed viral DNA without promoting transcription from the viral LTR. Importantly, CD4(+) T-cells from patients with Aicardi-Goutières Syndrome harboring mutation in the SAMHD1 gene display an increased susceptibility to HIV-1 infection that is not further enhanced by VLP-Vpx-treatment. CONCLUSION: Here, we identified SAMHD1 as the restriction factor preventing efficient viral DNA synthesis in non-cycling resting CD4(+) T-cells. These results highlight the crucial role of SAMHD1 in mediating restriction of HIV-1 infection in quiescent CD4(+) T-cells and could impact our understanding of HIV-1 mediated CD4(+) T-cell depletion and establishment of the viral reservoir, two of the HIV/AIDS hallmarks. BioMed Central 2012-10-23 /pmc/articles/PMC3494655/ /pubmed/23092122 http://dx.doi.org/10.1186/1742-4690-9-87 Text en Copyright ©2012 Descours et al.; 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 Descours, Benjamin Cribier, Alexandra Chable-Bessia, Christine Ayinde, Diana Rice, Gillian Crow, Yanick Yatim, Ahmad Schwartz, Olivier Laguette, Nadine Benkirane, Monsef SAMHD1 restricts HIV-1 reverse transcription in quiescent CD4(+) T-cells |
title | SAMHD1 restricts HIV-1 reverse transcription in quiescent CD4(+) T-cells |
title_full | SAMHD1 restricts HIV-1 reverse transcription in quiescent CD4(+) T-cells |
title_fullStr | SAMHD1 restricts HIV-1 reverse transcription in quiescent CD4(+) T-cells |
title_full_unstemmed | SAMHD1 restricts HIV-1 reverse transcription in quiescent CD4(+) T-cells |
title_short | SAMHD1 restricts HIV-1 reverse transcription in quiescent CD4(+) T-cells |
title_sort | samhd1 restricts hiv-1 reverse transcription in quiescent cd4(+) t-cells |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3494655/ https://www.ncbi.nlm.nih.gov/pubmed/23092122 http://dx.doi.org/10.1186/1742-4690-9-87 |
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