T-cell receptor complex is essential for Fas signal transduction

被引:26
作者
Akimzhanov, Askar M. [1 ]
Wang, Xinmin [1 ]
Sun, Jiaren [2 ]
Boehning, Darren [1 ]
机构
[1] Univ Texas Med Branch, Dept Neurosci & Cell Biol, Galveston, TX 77555 USA
[2] Univ Texas Med Branch, Dept Immunol, Galveston, TX 77555 USA
基金
美国国家卫生研究院;
关键词
apoptosis; calcium; Lck; TYROSINE KINASE; MEDIATED APOPTOSIS; PERIPHERAL-BLOOD; ANTIGEN RECEPTOR; GENETIC-EVIDENCE; FAMILY KINASES; DEATH RECEPTOR; ACTIVATION; CALCIUM; CHAIN;
D O I
10.1073/pnas.1005419107
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The Fas receptor (also known as CD95 and APO-1) is a member of the tumor necrosis factor a-family of death receptors that mediate T-cell responses. Here, we show that Fas receptor signaling requires a functional T-cell receptor (TCR) complex. Fas receptor directly binds to and activates TCR components in a stimulus-dependent manner. Fas receptor stimulation does not activate canonical downstream TCR pathways, but instead the TCR complex is required specifically for Fas-mediated calcium release. Importantly, null mutations in Lck, ZAP70, and the TCR alpha- and beta-chains abrogate Fas signaling. Our results reveal a direct role for the TCR complex in mediating Fas-specific signaling events critical for T-cell homeostasis.
引用
收藏
页码:15105 / 15110
页数:6
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