The roles of FADD in extrinsic apoptosis and necroptosis

Eun Woo Lee, Jinho Seo, Manhyung Jeong, Sangsik Lee, Jaewhan Song

Research output: Contribution to journalReview article

64 Citations (Scopus)

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.

Original languageEnglish
Pages (from-to)496-508
Number of pages13
JournalBMB reports
Volume45
Issue number9
DOIs
Publication statusPublished - 2012 Dec 27

Fingerprint

Fas-Associated Death Domain Protein
Apoptosis
Proteins
Death Domain Receptors
Defects
Autophagy
Cell death
Caspases
Transgenic Mice
Cell Cycle
Cell Death
Necrosis
Cells

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Molecular Biology

Cite this

Lee, Eun Woo ; Seo, Jinho ; Jeong, Manhyung ; Lee, Sangsik ; Song, Jaewhan. / The roles of FADD in extrinsic apoptosis and necroptosis. In: BMB reports. 2012 ; Vol. 45, No. 9. pp. 496-508.
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The roles of FADD in extrinsic apoptosis and necroptosis. / Lee, Eun Woo; Seo, Jinho; Jeong, Manhyung; Lee, Sangsik; Song, Jaewhan.

In: BMB reports, Vol. 45, No. 9, 27.12.2012, p. 496-508.

Research output: Contribution to journalReview article

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