Human immunodeficiency virus infection of cells arrested in the cell cycle

Paul Lewis, Michelle Hensel, Michael Emerman

Research output: Contribution to journalArticlepeer-review

417 Scopus citations

Abstract

Cell proliferation is necessary for proviral integration and productive infection of most retroviruses. Nevertheless, the human immunodeficiency virus (HIV) can infect non-dividing macrophages. This ability to grow in non-dividing cells is not specific to macrophages because, as we show here, CD4+ HeLa cells arrested at stage G2 of the cell cycle can be infected by HIV-1. Proliferation is necessary for these same cells to be infected by a murine retrovirus, MuLV. HIV-1 integrates into the arrested cell DNA and produces viral RNA and protein in a pattern similar to that in normal cells. In addition, our data suggest that the ability to infect non-dividing cells is due to one of the HIV-1 core virion proteins. HIV infection of non-dividing cells distinguishes lentiviruses from other retroviruses and is likely to be important in the natural history of HIV infection.

Original languageEnglish (US)
Pages (from-to)3053-3058
Number of pages6
JournalEMBO Journal
Volume11
Issue number8
StatePublished - 1992
Externally publishedYes

Keywords

  • AIDS
  • Cell cycle
  • HIV
  • Macrophages
  • MuLV

ASJC Scopus subject areas

  • General Neuroscience
  • Molecular Biology
  • General Biochemistry, Genetics and Molecular Biology
  • General Immunology and Microbiology

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