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FADD 在细胞外在凋亡和坏死性凋亡中的作用。

The roles of FADD in extrinsic apoptosis and necroptosis.

机构信息

Department of Biochemistry, College of Life Science and Biotechnology, Yonsei University, Seoul 120-749, Korea.

出版信息

BMB Rep. 2012 Sep;45(9):496-508. doi: 10.5483/bmbrep.2012.45.9.186.

Abstract

Fas-associated protein with death domain (FADD), an adaptor that bridges death receptor signaling to the caspase cascade, is indispensible for the induction of extrinsic apoptotic cell death. Interest in the non-apoptotic function of FADD has greatly increased due to evidence that FADD-deficient mice or dominant-negative FADD transgenic mice result in embryonic lethality and an immune defect without showing apoptotic features. Numerous studies have suggested that FADD regulates cell cycle progression, proliferation, and autophagy, affecting these phenomena. Recently, programmed necrosis, also called necroptosis, was shown to be a key mechanism that induces embryonic lethality and an immune defect. Supporting these findings, FADD was shown to be involved in various necroptosis models. In this review, we summarize the mechanism of extrinsic apoptosis and necroptosis, and discuss the in vivo and in vitro roles of FADD in necroptosis induced by various stimuli.

摘要

死亡结构域相关 Fas 蛋白(FADD)是一种衔接蛋白,可将死亡受体信号转导与胱天蛋白酶级联联系起来,对于诱导外在凋亡性细胞死亡是必不可少的。由于有证据表明 FADD 缺陷型小鼠或显性负性 FADD 转基因小鼠导致胚胎致死和免疫缺陷而没有表现出凋亡特征,因此人们对 FADD 的非凋亡功能产生了极大的兴趣。许多研究表明,FADD 调节细胞周期进程、增殖和自噬,从而影响这些现象。最近,程序性细胞坏死,也称为坏死性凋亡,被证明是诱导胚胎致死和免疫缺陷的关键机制。支持这些发现,FADD 被证明参与各种坏死性凋亡模型。在这篇综述中,我们总结了外在凋亡和坏死性凋亡的机制,并讨论了 FADD 在各种刺激诱导的坏死性凋亡中在体内和体外的作用。

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