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Polarized cells display asymmetric release of extracellular vesicles.
Colombo, Federico; Casella, Giacomo; Podini, Paola; Finardi, Annamaria; Racchetti, Gabriella; Norton, Erienne Grace; Cocucci, Emanuele; Furlan, Roberto.
Afiliação
  • Colombo F; Institute of Experimental Neurology, Division of Neuroscience, San Raffaele Scientific Institute, Milan, Italy.
  • Casella G; Institute of Experimental Neurology, Division of Neuroscience, San Raffaele Scientific Institute, Milan, Italy.
  • Podini P; Institute of Experimental Neurology, Division of Neuroscience, San Raffaele Scientific Institute, Milan, Italy.
  • Finardi A; Institute of Experimental Neurology, Division of Neuroscience, San Raffaele Scientific Institute, Milan, Italy.
  • Racchetti G; Division of Neuroscience, San Raffaele Scientific Institute, Milan, Italy.
  • Norton EG; Division of Pharmaceutics and Pharmacology, College of Pharmacy, The Ohio State University, Columbus, Ohio, USA.
  • Cocucci E; Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio, USA.
  • Furlan R; Division of Pharmaceutics and Pharmacology, College of Pharmacy, The Ohio State University, Columbus, Ohio, USA.
Traffic ; 22(4): 98-110, 2021 04.
Article em En | MEDLINE | ID: mdl-33314523
ABSTRACT
Extracellular vesicles (EVs), a broad term for the lipid microparticles known as microvesicles and exosomes, are discharged by cells into their surrounding space. Microvesicles are discharged upon outward plasma membrane budding, while exosomes are secreted after multivesicular body (MVB) fusion with the plasma membrane. The majority of information regarding EV biology comes from studies performed in non-polarized cells. Here we characterize EV release in polarized cells. We found a substantial asymmetry in the number and composition of EVs produced and released from the apical membrane of epithelial cells as compared to the basolateral membrane. We showed that the quantitative difference is related to the polarized distribution of two phosphoinositide species between the two cell surfaces and that the peculiar biochemical composition of resultant EVs reflects their site of origin. In particular, apical and basolateral exosomes may derive from distinct classes of MVBs originating from and fusing with the same plasma membrane. We identify VAMP8/Endobrevin as a regulator of the basolateral release of exosomes, whereas the mechanism responsible for apical EV release requires further study.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Micropartículas Derivadas de Células / Exossomos / Vesículas Extracelulares Idioma: En Revista: Traffic Assunto da revista: FISIOLOGIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Micropartículas Derivadas de Células / Exossomos / Vesículas Extracelulares Idioma: En Revista: Traffic Assunto da revista: FISIOLOGIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Itália