An unexpected role for FosB in activation-induced cell death of T cells

被引:0
|
作者
Sven Baumann
Jochen Hess
Sören T Eichhorst
Andreas Krueger
Peter Angel
Peter H Krammer
Sabine Kirchhoff
机构
[1] Tumor Immunology Program,
[2] SignaI Transduction and Growth Control,undefined
[3] German Cancer Research Center,undefined
来源
Oncogene | 2003年 / 22卷
关键词
activation-induced cell death; CD95 ligand; AP-1; T cells;
D O I
暂无
中图分类号
学科分类号
摘要
The CD95 (APO-1/Fas) system plays a major role in induction of apoptosis in lymphoid and nonlymphoid tissues. The CD95 (APO-1/Fas) ligand (CD95L) is induced in response to a variety of signals including TCR/CD3 stimulation or application of chemotherapeutic drugs. Here we report that an AP-1 site located in the 5′ untranslated region of the CD95L gene is required for TCR/CD3-mediated induction of the human CD95L promoter. Electrophoretic mobility shift assays using nuclear extracts of Jurkat T cells as well as TCR/CD3-restimulated primary human T cells demonstrated specific binding of AP-1, predominantly composed of c-Jun and FosB, to this sequence. Ectopic expression of transdominant negative Jun mutants strongly reduced CD95L promoter activity and activation-induced cell death (AICD), confirming the functional significance of FosB/c-Jun binding. Thus, our results demonstrate an important novel function for FosB dimerized with c-Jun in TCR/CD3-mediated AICD in human T cells.
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页码:1333 / 1339
页数:6
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