Volume 4, Issue 2 (2023) – 9 articles
Cover Picture: A current view of exosome and ectosome biogenetic mechanisms is shown at the bottom and top half of the image, respectively. The formation and assembly of exosomes begins in a specialized multivesicular endosome (MVE) where intraluminal vesicles (ILV), enriched in cargo carriers (tetraspanins such as CD63) and deliverables, among other generic markers, are formed by the inward vesiculation of a cholesterol, sphingomyelin enriched microdomain. The process is driven by members of the ESCRT family of proteins (ESCRT 0-II; ESCRT3) and/or by the enrichment of ceramide and other membrane bending factors via the action of sphingomyelinase. The V0 subunit of the V-ATPase may also play a role. Ectosomes (top half of the image) are formed at the plasma membrane by a variety of mechanisms including the ESCRTs often interacting with ARRDC1and CD133, the latter shown to be required for small ectosome biogenesis from microvilli in drosophila epithelium. Arf6 plays a role in some forms of ectosome secretion. Recent work also shows that I-Bar domain proteins may play a role in the membrane curvature required for ectosome biogenesis and release。
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