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Specificities of exosome versus small ectosome secretion revealed by live intracellular tracking of CD63 and CD9.

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Jouve, Mabel 
Valenzuela, José Ignacio 
Maurin, Mathieu 


Despite their roles in intercellular communications, the different populations of extracellular vesicles (EVs) and their secretion mechanisms are not fully characterized: how and to what extent EVs form as intraluminal vesicles of endocytic compartments (exosomes), or at the plasma membrane (PM) (ectosomes) remains unclear. Here we follow intracellular trafficking of the EV markers CD9 and CD63 from the endoplasmic reticulum to their residency compartment, respectively PM and late endosomes. We observe transient co-localization at both places, before they finally segregate. CD9 and a mutant CD63 stabilized at the PM are more abundantly released in EVs than CD63. Thus, in HeLa cells, ectosomes are more prominent than exosomes. By comparative proteomic analysis and differential response to neutralization of endosomal pH, we identify a few surface proteins likely specific of either exosomes (LAMP1) or ectosomes (BSG, SLC3A2). Our work sets the path for molecular and functional discrimination of exosomes and small ectosomes in any cell type.



Cell Communication, Cell Membrane, Endosomes, Exosomes, Extracellular Vesicles, Fusion Regulatory Protein 1, Heavy Chain, Gene Knockout Techniques, HeLa Cells, Humans, Membrane Proteins, Protein Transport, Proteomics, Tetraspanin 29, Tetraspanin 30

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Nat Commun

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Springer Science and Business Media LLC