IL-4 is able to reverse the CD2-mediated negative apoptotic signal to CD4-CD8- alpha beta and/or gamma delta T lymphocytes

Immunology. 1995 Nov;86(3):379-84.

Abstract

Activation of immature thymocytes or transformed T lymphocytes via T-cell receptor (TCR)/CD3 signalling can induce programmed cell death (apoptosis). Recent data indicate that anti-CD3/TCR monoclonal antibodies (mAb) also trigger apoptosis in activated (but not resting) mature peripheral blood T lymphocytes. Here we report that triggering of resting CD4-CD8-TCR alpha beta+ and/or TCR gamma delta+ via the alternative CD2-dependent activation pathway is able to induce programmed cell death. A pair of mitogenic anti-CD2 mAb provoked a dramatic rise in [Ca2+]i that was almost entirely sustained by extracellular fluxes, and the inhibition of membrane [Ca2+/Mg2+] ATPase. The resulting endonuclease activation was able to induce DNA fragmentation, as revealed by propidium iodide staining and gel electrophoresis. Induction of apoptosis was prevented by the presence of interleukin-4 (IL-4) as well as by endonuclease inactivation with 100 microM ZnCl2, but enhanced by the contemporary block of protein kinase C. Thus it seems that in resting T lymphocytes the strong calcium signal delivered by the alternative CD2 activation pathway may act as a negative apoptotic signal in both alpha beta and gamma delta T cells with low (non-major histocompatibility complex restricted) antigenic affinity, so limiting the extension of polyclonal T-cell growth.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Monoclonal
  • Apoptosis / immunology
  • CD2 Antigens / metabolism*
  • CD4 Antigens
  • CD8 Antigens
  • Calcium / metabolism
  • Calcium-Transporting ATPases / metabolism
  • Cells, Cultured
  • Humans
  • Inositol 1,4,5-Trisphosphate / metabolism
  • Interleukin-4 / metabolism*
  • Lymphocyte Activation
  • Lymphocyte Count
  • Receptors, Antigen, T-Cell, alpha-beta / metabolism*
  • Receptors, Antigen, T-Cell, gamma-delta / metabolism*
  • Signal Transduction / physiology*
  • T-Lymphocyte Subsets / immunology
  • T-Lymphocytes / metabolism*

Substances

  • Antibodies, Monoclonal
  • CD2 Antigens
  • CD4 Antigens
  • CD8 Antigens
  • Receptors, Antigen, T-Cell, alpha-beta
  • Receptors, Antigen, T-Cell, gamma-delta
  • Interleukin-4
  • Inositol 1,4,5-Trisphosphate
  • Calcium-Transporting ATPases
  • Calcium