Tumor necrosis factor receptor p55 mediates induction of HIV type 1 expression in chronically infected U1 cells

AIDS Res Hum Retroviruses. 1996 Feb 10;12(3):199-204. doi: 10.1089/aid.1996.12.199.

Abstract

Tumor necrosis factor alpha (TNF-alpha) is a potent inducer of human immunodeficiency virus type 1 (HIV-1) expression in chronically infected cells. The aim of this study was to investigate the role played by the two known TNF-alpha receptors, TNFR-p55 and TNFR-p75, in the activation of HIV-1 expression. As a model system the latently infected human promonocytic cell line U1 was stimulated with wild-type TNF-alpha, with TNF-alpha muteins that specifically bind to one or the other receptor or with receptor-specific monoclonal antibodies. Induction of HIV-1 expression, measured by p24 core antigen capture enzyme-linked immunosorbent assay (ELISA), was found to be exclusively triggered by TNFR-p55 stimulation. However, our results also showed that the addition of TNFR-p75-specific ligands negatively modulated the HIV-1 expression induced via TNFR-p55.

MeSH terms

  • Antigens, CD / metabolism*
  • Cell Line
  • HIV Core Protein p24 / drug effects*
  • HIV Core Protein p24 / metabolism
  • HIV-1 / drug effects*
  • HIV-1 / metabolism
  • Humans
  • Monocytes / cytology
  • Monocytes / drug effects*
  • Monocytes / metabolism
  • Receptors, Tumor Necrosis Factor / metabolism*
  • Receptors, Tumor Necrosis Factor, Type I
  • Receptors, Tumor Necrosis Factor, Type II
  • Tumor Necrosis Factor-alpha / pharmacology*

Substances

  • Antigens, CD
  • HIV Core Protein p24
  • Receptors, Tumor Necrosis Factor
  • Receptors, Tumor Necrosis Factor, Type I
  • Receptors, Tumor Necrosis Factor, Type II
  • Tumor Necrosis Factor-alpha