CD95 signaling via ceramide-rich membrane rafts

被引:514
作者
Grassmé, H
Jekle, A
Riehle, A
Schwarz, H
Berger, J
Sandhoff, K
Kolesnick, R
Gulbins, E
机构
[1] St Jude Childrens Res Hosp, Dept Immunol, Memphis, TN 38105 USA
[2] Univ Bonn, Kekule Inst Organ Chem & Biochem, D-53121 Bonn, Germany
[3] Max Planck Inst Dev Biol, D-72076 Teubingen, Germany
[4] Mem Sloan Kettering Canc Ctr, Lab Signal Transduct, New York, NY 10021 USA
关键词
D O I
10.1074/jbc.M101207200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 sphingo lipid-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.
引用
收藏
页码:20589 / 20596
页数:8
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