Chemokine-receptor activation by env determines the mechanism of death in HIV-infected and uninfected T lymphocytes

J Clin Invest. 2001 Jan;107(2):207-15. doi: 10.1172/JCI11109.

Abstract

There is considerable confusion concerning the mechanism of lymphocyte death during HIV infection. During the course of HIV infection, M-tropic viruses (R5) that use CCR5 chemokine coreceptors frequently evolve to T-tropic viruses (X4) that use CXCR4 receptors. In this study we show that activation of the CD4 or CCR5 receptor by R5 HIVenv causes a caspase 8-dependent death of both uninfected and infected CD4 T cells. In contrast, CXCR4 activation by X4 HIVenv induces a caspase-independent death of both uninfected CD4 and CD8 T cells and infected CD4 cells. These results suggest that activation of the chemokine receptor by HIVenv determines the mechanism of death for both infected and uninfected T lymphocytes.

Publication types

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

MeSH terms

  • Apoptosis
  • CD4-Positive T-Lymphocytes / physiology
  • CD4-Positive T-Lymphocytes / virology
  • CD8-Positive T-Lymphocytes / physiology
  • CD8-Positive T-Lymphocytes / virology
  • Caspase 8
  • Caspase 9
  • Caspases / physiology
  • Genes, env*
  • HIV / genetics*
  • Humans
  • Receptors, CCR5 / physiology
  • Receptors, CXCR4 / physiology
  • Receptors, Chemokine / physiology*
  • T-Lymphocytes / metabolism
  • T-Lymphocytes / virology*

Substances

  • Receptors, CCR5
  • Receptors, CXCR4
  • Receptors, Chemokine
  • CASP8 protein, human
  • CASP9 protein, human
  • Caspase 8
  • Caspase 9
  • Caspases