Ceramide Triggers Budding of Exosome Vesicles into Multivesicular Endosomes

Author:

Trajkovic Katarina12345,Hsu Chieh12345,Chiantia Salvatore12345,Rajendran Lawrence12345,Wenzel Dirk12345,Wieland Felix12345,Schwille Petra12345,Brügger Britta12345,Simons Mikael12345

Affiliation:

1. Centre for Biochemistry and Molecular Cell Biology, University of Göttingen, 37073 Göttingen, Germany.

2. Max-Planck-Institute for Experimental Medicine, 37075 Göttingen, Germany.

3. Max-Planck-Institute for Biophysical Chemistry, 37077 Göttingen, Germany.

4. Heidelberg University Biochemistry Center, 69120 Heidelberg, Germany.

5. BioTec, TU Dresden, 01307 Dresden, Germany.

Abstract

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.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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