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PMID: 11279185 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

CD95 signaling via ceramide-rich membrane rafts.

The Journal of biological chemistry ·Vol. 276 ·No. 23 ·2001-06-08 ·Pages 20589-96

Grassme H, Jekle A, Riehle A, Schwarz H, Berger J, Sandhoff K, Kolesnick R, Gulbins E

Abstract

Clustering seems to be employed by many receptors for transmembrane signaling. Here, we show that acid sphingomyelinase (ASM)-released ceramide is essential for clustering of CD95. In vitro and in vivo, extracellularly orientated ceramide, released upon CD95-triggered translocation of ASM to the plasma membrane outer surface, enabled clustering of CD95 in sphingolipid-rich membrane rafts and apoptosis induction. Whereas ASM deficiency, destruction of rafts, or neutralization of surface ceramide prevented CD95 clustering and apoptosis, natural ceramide only rescued ASM-deficient cells. The data suggest CD95-mediated clustering by ceramide is prerequisite for signaling and death.

MeSH Terms
Apoptosis Cell Membrane/metabolism Cells, Cultured Ceramides/metabolism Humans Signal Transduction Sphingolipids/metabolism fas Receptor/metabolism
Chemicals
Ceramides Sphingolipids fas Receptor
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Grassme H
Department of Immunology, St. Jude Children's Research Hospital, Memphis, Tennessee 38105, USA.
Jekle A
Riehle A
Schwarz H
Berger J
Sandhoff K
Kolesnick R
Gulbins E
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2001-06-08
Epub
2001-00-12
Pages
20589-96
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NCI NIH HHS · CA21765 · United States
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