The roles of FADD in extrinsic apoptosis and necroptosis

被引:131
作者
Lee, Eun-Woo [1 ]
Seo, Jinho [1 ]
Jeong, Manhyung [1 ]
Lee, Sangsik [2 ]
Song, Jaewhan [1 ]
机构
[1] Yonsei Univ, Coll Life Sci & Biotechnol, Dept Biochem, Seoul 120749, South Korea
[2] Kwandong Univ, Dept Biomed Engn, Kangnung 210701, South Korea
基金
新加坡国家研究基金会;
关键词
Caspase-8; FADD; Neaoptosis; Programmed necrosis; RIP3; TUMOR-NECROSIS-FACTOR; NF-KAPPA-B; RECEPTOR-INTERACTING PROTEIN; NECROTIC CELL-DEATH; TNF-ALPHA; PROGRAMMED NECROSIS; L929; CELLS; SIGNALING PATHWAYS; DOMAIN FADD; T-CELLS;
D O I
10.5483/BMBRep.2012.45.9.186
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
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. [BMB Reports 2012; 45(9): 496-508]
引用
收藏
页码:496 / 508
页数:13
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