Signals transduced through the CD4 molecule interfere with TCR/CD3-mediated ras activation leading to T cell anergy/apoptosis

Clin Immunol Immunopathol. 1997 Nov;85(2):195-201. doi: 10.1006/clin.1997.4424.

Abstract

It has been previously demonstrated that the occupancy of CD4 molecules by the HIV-1 envelope glycoprotein gp120 results in marked inhibition of T cell receptor-CD3 complex (TCR/CD3) activation-induced IL-2 secretion. To elucidate the mechanism of inhibitory effects of gp160 on T cell signaling, we have investigated the intracellular biochemical events and biological output in response to anti-CD3 mAb activation of purified peripheral blood CD4+ T cells from healthy donors with and without prior exposure to HIV-1 gp160. Pretreatment with gp160 resulted in marked inhibition of tyrosine phosphorylation of p59(fyn), PLC-gamma1, ras activation, and TNF-alpha secretion in anti-CD3 mAb activated CD4+ T cells, and a subset of CD4+ cells underwent activation-induced cell death. The data presented here provide insight into the mechanism by which the interaction of HIV-1 envelope glycoproteins with CD4 molecules may alter TCR/CD3-activation-induced signal transduction resulting in anergy and apoptosis with consequent functional deficiency of CD4+ T cells.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Apoptosis / physiology
  • CD3 Complex / physiology*
  • CD4-Positive T-Lymphocytes / cytology*
  • CD4-Positive T-Lymphocytes / immunology*
  • Gene Expression Regulation
  • Genes, ras / genetics*
  • HIV Envelope Protein gp120 / pharmacology
  • HIV Envelope Protein gp160 / pharmacology
  • HIV-1
  • Humans
  • Interleukin-2 / metabolism
  • Lymphocyte Activation / drug effects
  • Phosphorylation / drug effects
  • Protein-Tyrosine Kinases / metabolism
  • Receptors, Antigen, T-Cell / physiology*
  • Signal Transduction / physiology
  • Tumor Necrosis Factor-alpha / analysis
  • fas Receptor / biosynthesis

Substances

  • CD3 Complex
  • HIV Envelope Protein gp120
  • HIV Envelope Protein gp160
  • Interleukin-2
  • Receptors, Antigen, T-Cell
  • Tumor Necrosis Factor-alpha
  • fas Receptor
  • Protein-Tyrosine Kinases