Bad can act as a key regulator of T cell apoptosis and T cell development

J Exp Med. 1999 Feb 1;189(3):575-86. doi: 10.1084/jem.189.3.575.

Abstract

Bad is a distant relative of Bcl-2 and acts to promote cell death. Here, we show that Bad expression levels are greatly increased in thymocytes during apoptosis. We generated bad transgenic mice to study the action of upregulated Bad expression on T cell apoptosis. The T cells from these mice are highly sensitive to apoptotic stimuli, including anti-CD95. The numbers of T cells are greatly depleted and the processes of T cell development and selection are perturbed. We show that the proapoptotic function of Bad in primary T cells is regulated by Akt kinase and that Bad overexpression enhances both cell cycle progression and interleukin 2 production after T cell activation. These data suggest that Bad can act as a key regulator of T cell apoptosis and that this is a consequence of its upregulation after exposure to death stimuli.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis*
  • CD3 Complex / metabolism
  • Carrier Proteins / biosynthesis*
  • Cell Cycle
  • Dexamethasone / pharmacology
  • Gamma Rays / adverse effects
  • Homeodomain Proteins / genetics
  • Interleukin-12 / biosynthesis
  • Mice
  • Mice, Transgenic
  • Phosphatidylinositol 3-Kinases / metabolism
  • Protein Kinases / metabolism
  • Protein Serine-Threonine Kinases*
  • Proto-Oncogene Proteins / metabolism
  • Proto-Oncogene Proteins c-akt
  • Signal Transduction
  • T-Lymphocytes / immunology*
  • Thymus Gland / cytology
  • Thymus Gland / immunology*
  • Up-Regulation
  • bcl-Associated Death Protein
  • fas Receptor / immunology

Substances

  • Bad protein, mouse
  • CD3 Complex
  • Carrier Proteins
  • Homeodomain Proteins
  • Proto-Oncogene Proteins
  • bcl-Associated Death Protein
  • fas Receptor
  • RAG-1 protein
  • Interleukin-12
  • Dexamethasone
  • Protein Kinases
  • Protein Serine-Threonine Kinases
  • Proto-Oncogene Proteins c-akt