The multilevel regulation of CD95 signaling outcome

CD95, also called Fas or APO-1, was the first death receptor (DR) identified and characterized. Studies on CD95 receptor signaling revealed the versatile principles of cell fate regulation via DR. DRs could exert both pro- and anti-apoptotic effects depending on clustering, internalization or signal...

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Published in:Experimental Oncology
Date:2012
Main Authors: Yurchenko, M., Shlapatska, L.M., Sidorenko, S.P.
Format: Article
Language:English
Published: Інститут експериментальної патології, онкології і радіобіології ім. Р.Є. Кавецького НАН України 2012
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Online Access:https://nasplib.isofts.kiev.ua/handle/123456789/138726
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Journal Title:Digital Library of Periodicals of National Academy of Sciences of Ukraine
Cite this:The multilevel regulation of CD95 signaling outcome / M. Yurchenko, L.M. Shlapatska, S.P. Sidorenko // Experimental Oncology. — 2012. — Т. 34, № 3. — С. 153-159. — Бібліогр.: 71 назв. — англ.

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Digital Library of Periodicals of National Academy of Sciences of Ukraine
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Summary:CD95, also called Fas or APO-1, was the first death receptor (DR) identified and characterized. Studies on CD95 receptor signaling revealed the versatile principles of cell fate regulation via DR. DRs could exert both pro- and anti-apoptotic effects depending on clustering, internalization or signaling thresholds and other extracellular signals. It became clear that molecular network regulating cell death and survival is under the multilevel control. In this Review we focus on the regulation of CD95 signaling and provide brief analysis of molecular switches of its pro- and antiapoptotic functions. At least five levels of life-death cell regulation via CD95 could be tracked: extracellular, membrane, DISC, mitochondrial, and miRNA. The cellular outcome of signaling via DRs depends on other extracellular signals and availability of different intracellular components of signal transduction pathways. This article is part of a Special Issue entitled “Apoptosis: Four Decades Later”.
ISSN:1812-9269