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

被引:89
作者
Mok, CL
Gil-Gómez, G
Williams, O
Coles, M
Taga, S
Tolaini, M
Norton, T
Kioussis, D
Brady, HJM
机构
[1] Inst Child Hlth, Camelia Botnar Labs, Canc Biol Unit, London WC1N 1EH, England
[2] Inst Child Hlth, Camelia Botnar Labs, Mol Haematol Unit, London WC1N 1EH, England
[3] Natl Inst Med Res, MRC, Div Mol Immunol, London NW7 1AA, England
[4] Natl Inst Med Res, MRC, Div Cellular Immunol, London NW7 1AA, England
[5] Netherlands Canc Inst, Div Mol Genet, NL-1066 CX Amsterdam, Netherlands
关键词
Bad; apoptosis; selection; cell cycle; Akt;
D O I
10.1084/jem.189.3.575
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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 ban 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.
引用
收藏
页码:575 / 586
页数:12
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