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Local regulation of extracellular vesicle traffic by the synaptic endocytic machinery

Neuronal extracellular vesicles (EVs) are locally released from presynaptic terminals, carrying cargoes critical for intercellular signaling and disease. EVs are derived from endosomes, but it is unknown how these cargoes are directed to the EV pathway rather than for conventional endolysosomal degr...

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Autores principales: Blanchette, Cassandra R., Scalera, Amy L., Harris, Kathryn P., Zhao, Zechuan, Dresselhaus, Erica C., Koles, Kate, Yeh, Anna, Apiki, Julia K., Stewart, Bryan A., Rodal, Avital A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8952828/
https://www.ncbi.nlm.nih.gov/pubmed/35320349
http://dx.doi.org/10.1083/jcb.202112094
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author Blanchette, Cassandra R.
Scalera, Amy L.
Harris, Kathryn P.
Zhao, Zechuan
Dresselhaus, Erica C.
Koles, Kate
Yeh, Anna
Apiki, Julia K.
Stewart, Bryan A.
Rodal, Avital A.
author_facet Blanchette, Cassandra R.
Scalera, Amy L.
Harris, Kathryn P.
Zhao, Zechuan
Dresselhaus, Erica C.
Koles, Kate
Yeh, Anna
Apiki, Julia K.
Stewart, Bryan A.
Rodal, Avital A.
author_sort Blanchette, Cassandra R.
collection PubMed
description Neuronal extracellular vesicles (EVs) are locally released from presynaptic terminals, carrying cargoes critical for intercellular signaling and disease. EVs are derived from endosomes, but it is unknown how these cargoes are directed to the EV pathway rather than for conventional endolysosomal degradation. Here, we find that endocytic machinery plays an unexpected role in maintaining a release-competent pool of EV cargoes at synapses. Endocytic mutants, including nervous wreck (nwk), shibire/dynamin, and AP-2, unexpectedly exhibit local presynaptic depletion specifically of EV cargoes. Accordingly, nwk mutants phenocopy synaptic plasticity defects associated with loss of the EV cargo synaptotagmin-4 (Syt4) and suppress lethality upon overexpression of the EV cargo amyloid precursor protein (APP). These EV defects are genetically separable from canonical endocytic functions in synaptic vesicle recycling and synaptic growth. Endocytic machinery opposes the endosomal retromer complex to regulate EV cargo levels and acts upstream of synaptic cargo removal by retrograde axonal transport. Our data suggest a novel molecular mechanism that locally promotes cargo loading into synaptic EVs.
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spelling pubmed-89528282022-11-02 Local regulation of extracellular vesicle traffic by the synaptic endocytic machinery Blanchette, Cassandra R. Scalera, Amy L. Harris, Kathryn P. Zhao, Zechuan Dresselhaus, Erica C. Koles, Kate Yeh, Anna Apiki, Julia K. Stewart, Bryan A. Rodal, Avital A. J Cell Biol Article Neuronal extracellular vesicles (EVs) are locally released from presynaptic terminals, carrying cargoes critical for intercellular signaling and disease. EVs are derived from endosomes, but it is unknown how these cargoes are directed to the EV pathway rather than for conventional endolysosomal degradation. Here, we find that endocytic machinery plays an unexpected role in maintaining a release-competent pool of EV cargoes at synapses. Endocytic mutants, including nervous wreck (nwk), shibire/dynamin, and AP-2, unexpectedly exhibit local presynaptic depletion specifically of EV cargoes. Accordingly, nwk mutants phenocopy synaptic plasticity defects associated with loss of the EV cargo synaptotagmin-4 (Syt4) and suppress lethality upon overexpression of the EV cargo amyloid precursor protein (APP). These EV defects are genetically separable from canonical endocytic functions in synaptic vesicle recycling and synaptic growth. Endocytic machinery opposes the endosomal retromer complex to regulate EV cargo levels and acts upstream of synaptic cargo removal by retrograde axonal transport. Our data suggest a novel molecular mechanism that locally promotes cargo loading into synaptic EVs. Rockefeller University Press 2022-03-23 /pmc/articles/PMC8952828/ /pubmed/35320349 http://dx.doi.org/10.1083/jcb.202112094 Text en © 2022 Blanchette et al. https://creativecommons.org/licenses/by-nc-sa/4.0/http://www.rupress.org/terms/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Blanchette, Cassandra R.
Scalera, Amy L.
Harris, Kathryn P.
Zhao, Zechuan
Dresselhaus, Erica C.
Koles, Kate
Yeh, Anna
Apiki, Julia K.
Stewart, Bryan A.
Rodal, Avital A.
Local regulation of extracellular vesicle traffic by the synaptic endocytic machinery
title Local regulation of extracellular vesicle traffic by the synaptic endocytic machinery
title_full Local regulation of extracellular vesicle traffic by the synaptic endocytic machinery
title_fullStr Local regulation of extracellular vesicle traffic by the synaptic endocytic machinery
title_full_unstemmed Local regulation of extracellular vesicle traffic by the synaptic endocytic machinery
title_short Local regulation of extracellular vesicle traffic by the synaptic endocytic machinery
title_sort local regulation of extracellular vesicle traffic by the synaptic endocytic machinery
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8952828/
https://www.ncbi.nlm.nih.gov/pubmed/35320349
http://dx.doi.org/10.1083/jcb.202112094
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