SAMHD1: a new insight into HIV-1 restriction in myeloid cells.

Corine St Gelais, Li Wu
Author Information
  1. Corine St Gelais: Center for Retrovirus Research, Department of Veterinary Bioscience, The Ohio State University, 1900 Coffey Road, Columbus, OH 43210, USA.

Abstract

Human myeloid-lineage cells are refractory to HIV-1 infection. The Vpx proteins from HIV-2 and sooty mangabey SIV render these cells permissive to HIV-1 infection through proteasomal degradation of a putative restriction factor. Two recent studies discovered the cellular protein SAMHD1 to be this restriction factor, demonstrating that Vpx induces proteasomal degradation of SAMHD1 and enhances HIV-1 infection in myeloid-lineage cells. SAMHD1 functions as a myeloid-cell-specific HIV-1 restriction factor by inhibiting viral DNA synthesis. Here we discuss the implications of these findings in delineating the mechanisms of HIV-1 restriction in myeloid-lineage cells and the potential role of Vpx in lentiviral pathogenesis.

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Grants

  1. R21 AI078762-03/NIAID NIH HHS
  2. R21 AI078762/NIAID NIH HHS
  3. AI068493/NIAID NIH HHS
  4. R01 AI068493-06/NIAID NIH HHS
  5. R01 AI068493/NIAID NIH HHS
  6. AI078762/NIAID NIH HHS

MeSH Term

HIV-1
Humans
Models, Biological
Monomeric GTP-Binding Proteins
Myeloid Cells
SAM Domain and HD Domain-Containing Protein 1

Chemicals

SAM Domain and HD Domain-Containing Protein 1
SAMHD1 protein, human
Monomeric GTP-Binding Proteins

Word Cloud

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