CD2 ligation abrogates antigen-independent apoptosis in B cells

Cell Immunol. 1996 Jul 10;171(1):55-61. doi: 10.1006/cimm.1996.0172.

Abstract

We have described recently the prevention of apoptosis by CD2-soluble CD48 interaction on antigen B cell receptor occupancy. Here, we show that CD2 ligation is also able to interfere with B cell receptor-independent apoptosis pathways such as spontaneous death in spleen B cells or serum deprivation and hydrogen peroxide exposure in the BAL-17 cell line. In all cases, CD2 ligation induces a signal that prevents the downregulation of Bcl-2 expression. The specific CD2 signal pathway involved in this phenomenon is still unknown. As reported, CD2 did not appear to induce Ca2+ mobilization, phosphatidylinositol turnover, or PKC translocation in B cells. Nevertheless, we show that CD2 receptor ligation is coupled to the tyrosine phosphorylation pathway in B cells. These observations indicate that CD2 is functionally able to trigger at least an early signal that could play a role in apoptosis blockage B cells in addition to the adhesion one. The results suggest the participation of cellular membrane receptors other that CD40 in apoptosis rescue, not only in the antigen-dependent but also in the antigen-independent phases of B cell lymphopoiesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, CD / metabolism
  • Apoptosis / drug effects
  • Apoptosis / immunology*
  • B-Lymphocytes / drug effects
  • B-Lymphocytes / immunology*
  • B-Lymphocytes / metabolism*
  • CD2 Antigens / drug effects
  • CD2 Antigens / metabolism*
  • CD48 Antigen
  • Culture Media, Serum-Free / pharmacology
  • Free Radicals / metabolism
  • Ligands
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Phosphorylation
  • Signal Transduction / drug effects
  • Signal Transduction / immunology
  • Tumor Cells, Cultured
  • Tyrosine / metabolism

Substances

  • Antigens, CD
  • CD2 Antigens
  • CD48 Antigen
  • Cd48 protein, mouse
  • Culture Media, Serum-Free
  • Free Radicals
  • Ligands
  • Tyrosine