Grassme H, Jekle A, Riehle A, Schwarz H, Berger J, Sandhoff K, Kolesnick R, Gulbins E
Department of Immunology, St. Jude Children's Research Hospital, Memphis, Tennessee 38105, USA.
J Biol Chem. 2001 Jun 8;276(23):20589-96. doi: 10.1074/jbc.M101207200. Epub 2001 Mar 12.
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.
许多跨膜信号传导受体似乎都采用聚集的方式。在此,我们表明酸性鞘磷脂酶(ASM)释放的神经酰胺对于CD95的聚集至关重要。在体外和体内,CD95触发ASM转位至质膜外表面时释放的细胞外定向神经酰胺,可使CD95在富含鞘脂的膜筏中聚集并诱导细胞凋亡。而ASM缺乏、膜筏破坏或表面神经酰胺的中和会阻止CD95聚集和细胞凋亡,天然神经酰胺仅能挽救ASM缺陷细胞。这些数据表明,神经酰胺介导的CD95聚集是信号传导和细胞死亡的先决条件。