内体
ESCRT公司
细胞生物学
外体
神经酰胺
小泡
微泡
胞吐
膜泡运输蛋白质类
生物
TSG101型
化学
分泌物
膜
细胞内
生物化学
液泡蛋白分选
细胞凋亡
小RNA
基因
作者
Katarina Trajković,Chieh Hsu,Salvatore Chiantia,Lawrence Rajendran,Dirk Wenzel,Felix Wieland,Petra Schwille,Britta Brügger,Mikael Simons
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2008-02-28
卷期号:319 (5867): 1244-1247
被引量:3205
标识
DOI:10.1126/science.1153124
摘要
Intraluminal vesicles of multivesicular endosomes are either sorted for cargo degradation into lysosomes or secreted as exosomes into the extracellular milieu. The mechanisms underlying the sorting of membrane into the different populations of intraluminal vesicles are unknown. Here, we find that cargo is segregated into distinct subdomains on the endosomal membrane and that the transfer of exosome-associated domains into the lumen of the endosome did not depend on the function of the ESCRT (endosomal sorting complex required for transport) machinery, but required the sphingolipid ceramide. Purified exosomes were enriched in ceramide, and the release of exosomes was reduced after the inhibition of neutral sphingomyelinases. These results establish a pathway in intraendosomal membrane transport and exosome formation.
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