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Astrocytes‐derived extracellular vesicles in motion at the neuron surface: Involvement of the prion protein
Astrocytes‐derived extracellular vesicles (EVs) are key players in glia‐neuron communication. However, whether EVs interact with neurons at preferential sites and how EVs reach these sites on neurons remains elusive. Using optical manipulation to study single EV‐neuron dynamics, we here show that la...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8275823/ https://www.ncbi.nlm.nih.gov/pubmed/34276899 http://dx.doi.org/10.1002/jev2.12114 |
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author | D'Arrigo, Giulia Gabrielli, Martina Scaroni, Federica Swuec, Paolo Amin, Ladan Pegoraro, Anna Adinolfi, Elena Di Virgilio, Francesco Cojoc, Dan Legname, Giuseppe Verderio, Claudia |
author_facet | D'Arrigo, Giulia Gabrielli, Martina Scaroni, Federica Swuec, Paolo Amin, Ladan Pegoraro, Anna Adinolfi, Elena Di Virgilio, Francesco Cojoc, Dan Legname, Giuseppe Verderio, Claudia |
author_sort | D'Arrigo, Giulia |
collection | PubMed |
description | Astrocytes‐derived extracellular vesicles (EVs) are key players in glia‐neuron communication. However, whether EVs interact with neurons at preferential sites and how EVs reach these sites on neurons remains elusive. Using optical manipulation to study single EV‐neuron dynamics, we here show that large EVs scan the neuron surface and use neuronal processes as highways to move extracellularly. Large EV motion on neurites is driven by the binding of EV to a surface receptor that slides on neuronal membrane, thanks to actin cytoskeleton rearrangements. The use of prion protein (PrP)‐coated synthetic beads and PrP knock out EVs/neurons points at vesicular PrP and its receptor(s) on neurons in the control of EV motion. Surprisingly, a fraction of large EVs contains actin filaments and has an independent capacity to move in an actin‐mediated way, through intermittent contacts with the plasma membrane. Our results unveil, for the first time, a dual mechanism exploited by astrocytic large EVs to passively/actively reach target sites on neurons moving on the neuron surface. |
format | Online Article Text |
id | pubmed-8275823 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82758232021-07-15 Astrocytes‐derived extracellular vesicles in motion at the neuron surface: Involvement of the prion protein D'Arrigo, Giulia Gabrielli, Martina Scaroni, Federica Swuec, Paolo Amin, Ladan Pegoraro, Anna Adinolfi, Elena Di Virgilio, Francesco Cojoc, Dan Legname, Giuseppe Verderio, Claudia J Extracell Vesicles Research Articles Astrocytes‐derived extracellular vesicles (EVs) are key players in glia‐neuron communication. However, whether EVs interact with neurons at preferential sites and how EVs reach these sites on neurons remains elusive. Using optical manipulation to study single EV‐neuron dynamics, we here show that large EVs scan the neuron surface and use neuronal processes as highways to move extracellularly. Large EV motion on neurites is driven by the binding of EV to a surface receptor that slides on neuronal membrane, thanks to actin cytoskeleton rearrangements. The use of prion protein (PrP)‐coated synthetic beads and PrP knock out EVs/neurons points at vesicular PrP and its receptor(s) on neurons in the control of EV motion. Surprisingly, a fraction of large EVs contains actin filaments and has an independent capacity to move in an actin‐mediated way, through intermittent contacts with the plasma membrane. Our results unveil, for the first time, a dual mechanism exploited by astrocytic large EVs to passively/actively reach target sites on neurons moving on the neuron surface. John Wiley and Sons Inc. 2021-07-12 2021-07 /pmc/articles/PMC8275823/ /pubmed/34276899 http://dx.doi.org/10.1002/jev2.12114 Text en © 2021 The Authors. Journal of Extracellular Vesicles published by Wiley Periodicals, LLC on behalf of the International Society for Extracellular Vesicles https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles D'Arrigo, Giulia Gabrielli, Martina Scaroni, Federica Swuec, Paolo Amin, Ladan Pegoraro, Anna Adinolfi, Elena Di Virgilio, Francesco Cojoc, Dan Legname, Giuseppe Verderio, Claudia Astrocytes‐derived extracellular vesicles in motion at the neuron surface: Involvement of the prion protein |
title | Astrocytes‐derived extracellular vesicles in motion at the neuron surface: Involvement of the prion protein |
title_full | Astrocytes‐derived extracellular vesicles in motion at the neuron surface: Involvement of the prion protein |
title_fullStr | Astrocytes‐derived extracellular vesicles in motion at the neuron surface: Involvement of the prion protein |
title_full_unstemmed | Astrocytes‐derived extracellular vesicles in motion at the neuron surface: Involvement of the prion protein |
title_short | Astrocytes‐derived extracellular vesicles in motion at the neuron surface: Involvement of the prion protein |
title_sort | astrocytes‐derived extracellular vesicles in motion at the neuron surface: involvement of the prion protein |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8275823/ https://www.ncbi.nlm.nih.gov/pubmed/34276899 http://dx.doi.org/10.1002/jev2.12114 |
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