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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2022
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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. |
format | Online Article Text |
id | pubmed-8952828 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Rockefeller University Press |
record_format | MEDLINE/PubMed |
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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