蛋白水解信号传导:死亡受体诱导细胞凋亡。

M Muzio
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引用次数: 88

摘要

细胞凋亡或程序性细胞死亡是一种遗传调控机制,在后生动物的发育和体内平衡中都起着核心作用。死亡受体(Fas、TNFR-2、DR3和TRAIL受体)通过连接同源配体或异位表达诱导细胞凋亡。诱导死亡的信号复合物的组装在受体激活后以分层方式发生。受体的死亡结构域与适配器分子FADD的相应结构域结合,后者反过来募集死亡蛋白酶FLICE (MACH/caspase-8)的酶原形式。近似地说,FLICE“酶原”达到足够的浓度来自我激活并触发凋亡途径。首次描述了一种跨膜受体直接参与信号复合物中的蛋白酶并随后触发蛋白水解信号级联。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Signalling by proteolysis: death receptors induce apoptosis.

Apoptosis, or programmed cell death, is a genetically regulated mechanism with a central role in both metazoan development and homeostasis. Death receptors (Fas, TNFR-2, DR3, and TRAIL receptors) induce apoptosis upon ligation to cognate ligands or ectopic expression. The assembly of a death-inducing signalling complex occurs in a hierarchical manner upon receptor activation. The death domain of the receptor binds to the corresponding domain of the adapter molecule FADD, which in turn recruits the zymogen form of the death protease FLICE (MACH/caspase-8). Upon approximation, FLICE "zymogens" attain a sufficient concentration to self-activate and to trigger the apoptotic pathway. For the first time, a transmembrane receptor directly engaging a protease at the signalling complex and subsequently triggering a proteolytic signalling cascade is described.

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