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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...

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Detalles Bibliográficos
Autores principales: Descours, Benjamin, Cribier, Alexandra, Chable-Bessia, Christine, Ayinde, Diana, Rice, Gillian, Crow, Yanick, Yatim, Ahmad, Schwartz, Olivier, Laguette, Nadine, Benkirane, Monsef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
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
Descripción
Sumario: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.