SDF-1α degrades whereas glycoprotein 120 upregulates Bcl-2 interacting mediator of death extralong isoform: implications for the development of T cell memory

J Immunol. 2012 Aug 15;189(4):1835-42. doi: 10.4049/jimmunol.1100275. Epub 2012 Jul 16.

Abstract

After a primary immune response, T cell memory occurs when a subset of Ag-specific T cells resists peripheral selection by acquiring resistance to TCR-induced death. Recent data have implicated Bcl-2 interacting mediator of death (Bim) as an essential mediator of the contraction phase of T cell immunity. In this article, we describe that stromal-derived factor-1α (SDF-1α) ligation of CXCR4 on activated T cells promotes two parallel processes that favor survival, phospho-inactivation of Foxo3A, as well as Bim extralong isoform (Bim(EL)) degradation, both in an Akt- and Erk-dependent manner. Activated primary CD4 T cells treated with SDF-1α therefore become resistant to the proapoptotic effects of TCR ligation or IL-2 deprivation and accumulate cells of a memory phenotype. Unlike SDF-1α, gp120 ligation of CXCR4 has the opposite effect because it causes p38-dependent Bim(EL) upregulation. However, when activated CD4 T cells are treated with both gp120 and SDF-1α, the SDF-1α-driven effects of Bim(EL) degradation and acquired resistance to TCR-induced death predominate. These results provide a novel causal link between SDF-1α-induced chemotaxis, degradation of Bim(EL), and the development of CD4 T cell memory.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Apoptosis / immunology
  • Apoptosis Regulatory Proteins / immunology*
  • Apoptosis Regulatory Proteins / metabolism
  • Bcl-2-Like Protein 11
  • CD4-Positive T-Lymphocytes / immunology*
  • CD4-Positive T-Lymphocytes / metabolism
  • Chemokine CXCL12 / immunology*
  • Chemokine CXCL12 / metabolism
  • Chemotaxis, Leukocyte / immunology
  • Flow Cytometry
  • Humans
  • Immunoblotting
  • Immunologic Memory / immunology*
  • Immunoprecipitation
  • Lymphocyte Activation / immunology
  • Membrane Proteins / immunology*
  • Membrane Proteins / metabolism
  • Protein Isoforms
  • Proto-Oncogene Proteins / immunology*
  • Proto-Oncogene Proteins / metabolism
  • Receptors, CXCR4 / immunology
  • Receptors, CXCR4 / metabolism
  • Signal Transduction / immunology
  • Transfection
  • Up-Regulation

Substances

  • Apoptosis Regulatory Proteins
  • BCL2L11 protein, human
  • Bcl-2-Like Protein 11
  • CXCR4 protein, human
  • Chemokine CXCL12
  • Membrane Proteins
  • Protein Isoforms
  • Proto-Oncogene Proteins
  • Receptors, CXCR4