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Ceramide Triggers Budding of Exosome Vesicles into Multivesicular Endosomes
Katarina Trajkovic,1,2*Chieh Hsu,1,2*Salvatore Chiantia,5Lawrence Rajendran,6Dirk Wenzel,3Felix Wieland,4Petra Schwille,5Britta Brügger,4Mikael Simons1,2,7
Intraluminal vesicles of multivesicular endosomes are eithersorted for cargo degradation into lysosomes or secreted as exosomesinto the extracellular milieu. The mechanisms underlying thesorting of membrane into the different populations of intraluminalvesicles are unknown. Here, we find that cargo is segregatedinto distinct subdomains on the endosomal membrane and thatthe transfer of exosome-associated domains into the lumen ofthe endosome did not depend on the function of the ESCRT (endosomalsorting complex required for transport) machinery, but requiredthe sphingolipid ceramide. Purified exosomes were enriched inceramide, and the release of exosomes was reduced after theinhibition of neutral sphingomyelinases. These results establisha pathway in intraendosomal membrane transport and exosome formation.
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. 6 Max-Planck-Institute of Cell Biology and Genetics, 01307 Dresden, Germany. 7 Department of Neurology, University of Göttingen, 37073 Göttingen, Germany.
* These authors contributed equally to this work.
To whom correspondence should be addressed. E-mail: msimons{at}gwdg.de
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