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PMID: 16226446 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S. Review

Nonapoptotic functions of FADD-binding death receptors and their signaling molecules.

Current opinion in cell biology ·Vol. 17 ·No. 6 ·2005-12-00 ·Pages 610-6

Park SM, Schickel R, Peter ME

Abstract

Death receptors (DRs) are surface receptors that when triggered have the capacity to induce apoptosis in cells by forming the death-inducing signaling complex (DISC). The first protein recruited to form the DISC is the adaptor protein FADD/Mort1. Some members of the DR family, CD95 and the TRAIL receptors DR4 and DR5, directly bind FADD, whereas others, such as TNF receptor I and DR3, initially bind another adaptor protein, TRADD, which then recruits FADD. While all DRs can activate both apoptotic and non-apoptotic pathways, it has been widely assumed that the main physiological role of FADD-binding death receptors is to trigger apoptosis. However, recent work has ascribed multiple non-apoptotic activities to these receptors and/or the signaling components of the DISC.

MeSH Terms
Adaptor Proteins, Signal Transducing/metabolism Animals Apoptosis CASP8 and FADD-Like Apoptosis Regulating Protein Caspase 8 Caspases/physiology Cell Cycle Proteins/physiology Fas-Associated Death Domain Protein Humans Intracellular Signaling Peptides and Proteins/physiology Models, Biological Signal Transduction/physiology fas Receptor/metabolism
Chemicals
Adaptor Proteins, Signal Transducing CASP8 and FADD-Like Apoptosis Regulating Protein CFLAR protein, human Cell Cycle Proteins FADD protein, human Fas-Associated Death Domain Protein Intracellular Signaling Peptides and Proteins fas Receptor CASP8 protein, human Caspase 8 Caspases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Park Sun-Mi
The Ben May Institute for Cancer Research, University of Chicago, 924 E. 57th Street., Chicago, Illinois 60637, USA.
Schickel Robert
Peter Marcus E
Article Info
Journal
Current opinion in cell biology
Abbr.
Curr Opin Cell Biol
ISSN
0955-0674
Published
2005-12-00
Epub
2005-00-13
Pages
610-6
Language
English
Region
England
NLM ID
8913428
Subset
IM
Grants
NCI NIH HHS · CA95319 · United States
NIGMS NIH HHS · GM61712 · United States
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