Bad Can Act as a Key Regulator of  T Cell Apoptosis and T Cell Development

Author:

Mok Chen-Lang1,Gil-Gómez Gabriel1,Williams Owen1,Coles Mark1,Taga Samir1,Tolaini Mauro1,Norton Trisha1,Kioussis Dimitris1,Brady Hugh J.M.11

Affiliation:

1. From the Division of Molecular Immunology and the Division of Cellular Immunology, MRC National Institute for Medical Research, London NW7 1AA, United Kingdom; the Division of Molecular Genetics, Netherlands Cancer Institute, 1066 CX Amsterdam, The Netherlands; and the Cancer Biology and Molecular Haematology Units, Camelia Botnar Laboratories, Institute of Child Health, London WC1N 1EH, United K

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.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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