TABLE 1.
Feature | Exosomes | References |
Size | 40–200 nm | Shao et al., 2018 |
Markers | ESCRT mechanism components (Alix, TSG101), tetraspanins (CD9, CD63, and CD81), heat shock proteins (Hsp70 and Hsp90), Rab GTPases, flotillin | Kalluri and LeBleu, 2020 |
Cargos | Proteins; lipids; DNA, mRNA, microRNA, and other non-coding RNAs | van Niel et al., 2018 |
Mechanism of release | ESCRT-dependent pathways | |
ESCRT-0, I, II, and III: MVBs formation, vesicle budding, and protein cargo sorting | Zhang et al., 2019 | |
ESCRT-independent pathways | ||
Ceramides: RNA sorting in mammalian cells, spontaneous negative curvature of the endosomal membrane and inducing the budding of ILVs | Trajkovic et al., 2008; Kosaka et al., 2010 | |
Tetraspanins such as CD9, CD63, CD82: the sorting of cargos to ILVs | Chairoungdua et al., 2010; van Niel et al., 2011 | |
Rab family proteins such as Rab27A, Rab27B, and Rab35: inducing the transfer of MVBs to the cell surface | Hsu et al., 2010; Ostrowski et al., 2010 | |
Cytoskeleton, molecular switches (small GTPases), membrane fusion associated molecules (SNAREs, tethering factors): the docking and fusion process between MVBs and PM | Raposo and Stoorvogel, 2013 | |
Mechanism of targeting recipient cells | Endocytosis (micropinocytosis, endocytosis mediated by clathrin, caveolin, or lipid rafts, phagocytosis of specialized cells such as macrophages) | van Niel et al., 2018 |
Fusing directly with the PM of the recipient cells | van Niel et al., 2018 | |
Receptor-ligand interactions | Mulcahy et al., 2014 | |
Physiological effect | Removing unnecessary components from cells: Modulating the expression and function of recipient cells by transferring bioactive molecules | Kalluri and LeBleu, 2020 |
ESCRT, endosomal sorting complex required for transport; SNAREs, soluble N-ethyl maleimide-sensitive factor attachment protein receptors.