Fas/FasL interaction is not involved in apoptosis of activated CD4+ T cells upon HIV-1 infection in vitro

J Acquir Immune Defic Syndr Hum Retrovirol. 1998 Aug 1;18(4):307-15. doi: 10.1097/00042560-199808010-00001.

Abstract

In HIV-1-infected individuals, Fas expression and Fas/FasL-mediated apoptosis of mature T cells are known to increase compared with those in normal individuals. To elucidate a relation between acute HIV-1 infection and the regulation of Fas/FasL system upon T-cell activation, resting CD4+ T cells were acutely infected or uninfected with HIV-1 and subsequently activated by phorbol myristate acetate and ionomycin (PMA/IM). Four days after infection, when HIV-1 env gp120 is expressed in more than one half of activated T cells, Fas/FasL expression was analyzed by flow cytometry, and apoptosis-inducing activity of these activated primary CD4+ T cells on Fas+ Jurkat cells was examined. The level of Fas or FasL expression was not altered during acute HIV-1 infection. The enhanced apoptosis-inducing activity upon HIV-1 infection was observed in some individuals, but its activity was not Fas/FasL-mediated. These results indicate that HIV-1 infection is not necessarily associated with either upregulation of Fas/FasL expression or Fas/FasL-mediated apoptosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Monoclonal / immunology
  • Antigens, Surface / physiology
  • Apoptosis / physiology*
  • CD4-Positive T-Lymphocytes / physiology
  • CD4-Positive T-Lymphocytes / virology*
  • Cell Line
  • Cells, Cultured
  • DNA Fragmentation / physiology
  • Fas Ligand Protein
  • Flow Cytometry
  • HIV Envelope Protein gp120 / analysis
  • HIV Envelope Protein gp120 / immunology
  • HIV-1 / physiology*
  • Humans
  • Leukocytes, Mononuclear / physiology
  • Ligands
  • Lymphocyte Activation
  • Membrane Glycoproteins / biosynthesis
  • Membrane Glycoproteins / physiology*
  • Receptors, Interleukin-2 / biosynthesis
  • Up-Regulation
  • fas Receptor / biosynthesis
  • fas Receptor / physiology*

Substances

  • Antibodies, Monoclonal
  • Antigens, Surface
  • FASLG protein, human
  • Fas Ligand Protein
  • HIV Envelope Protein gp120
  • Ligands
  • Membrane Glycoproteins
  • Receptors, Interleukin-2
  • fas Receptor