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White Matter Repair After Extracellular Vesicles Administration in an Experimental Animal Model of Subcortical Stroke

Mesenchymal stem cells have previously been shown to mediate brain repair after stroke; they secrete 50–100 nm complexes called extracellular vesicles (EVs), which could be responsible for provoking neurovascular repair and functional recovery. EVs have been observed by electron microscopy and NanoS...

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Autores principales: Otero-Ortega, Laura, Laso-García, Fernando, Gómez-de Frutos, María del Carmen, Rodríguez-Frutos, Berta, Pascual-Guerra, Jorge, Fuentes, Blanca, Díez-Tejedor, Exuperio, Gutiérrez-Fernández, María
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5353554/
https://www.ncbi.nlm.nih.gov/pubmed/28300134
http://dx.doi.org/10.1038/srep44433
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author Otero-Ortega, Laura
Laso-García, Fernando
Gómez-de Frutos, María del Carmen
Rodríguez-Frutos, Berta
Pascual-Guerra, Jorge
Fuentes, Blanca
Díez-Tejedor, Exuperio
Gutiérrez-Fernández, María
author_facet Otero-Ortega, Laura
Laso-García, Fernando
Gómez-de Frutos, María del Carmen
Rodríguez-Frutos, Berta
Pascual-Guerra, Jorge
Fuentes, Blanca
Díez-Tejedor, Exuperio
Gutiérrez-Fernández, María
author_sort Otero-Ortega, Laura
collection PubMed
description Mesenchymal stem cells have previously been shown to mediate brain repair after stroke; they secrete 50–100 nm complexes called extracellular vesicles (EVs), which could be responsible for provoking neurovascular repair and functional recovery. EVs have been observed by electron microscopy and NanoSight, and they contain associated proteins such as CD81 and Alix. This purified, homogeneous population of EVs was administered intravenously after subcortical stroke in rats. To evaluate the EVs effects, we studied the biodistribution, proteomics analysis, functional evaluation, lesion size, fiber tract integrity, axonal sprouting and white matter repair markers. We found that a single administration of EVs improved functional recovery, fiber tract integrity, axonal sprouting and white matter repair markers in an experimental animal model of subcortical stroke. EVs were found in the animals’ brain and peripheral organs after euthanasia. White matter integrity was in part restored by EVs administration mediated by molecular repair factors implicated in axonal sprouting, tract connectivity, remyelination and oligodendrogenesis. These findings are associated with improved functional recovery. This novel role for EVs presents a new perspective in the development of biologics for brain repair.
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spelling pubmed-53535542017-03-20 White Matter Repair After Extracellular Vesicles Administration in an Experimental Animal Model of Subcortical Stroke Otero-Ortega, Laura Laso-García, Fernando Gómez-de Frutos, María del Carmen Rodríguez-Frutos, Berta Pascual-Guerra, Jorge Fuentes, Blanca Díez-Tejedor, Exuperio Gutiérrez-Fernández, María Sci Rep Article Mesenchymal stem cells have previously been shown to mediate brain repair after stroke; they secrete 50–100 nm complexes called extracellular vesicles (EVs), which could be responsible for provoking neurovascular repair and functional recovery. EVs have been observed by electron microscopy and NanoSight, and they contain associated proteins such as CD81 and Alix. This purified, homogeneous population of EVs was administered intravenously after subcortical stroke in rats. To evaluate the EVs effects, we studied the biodistribution, proteomics analysis, functional evaluation, lesion size, fiber tract integrity, axonal sprouting and white matter repair markers. We found that a single administration of EVs improved functional recovery, fiber tract integrity, axonal sprouting and white matter repair markers in an experimental animal model of subcortical stroke. EVs were found in the animals’ brain and peripheral organs after euthanasia. White matter integrity was in part restored by EVs administration mediated by molecular repair factors implicated in axonal sprouting, tract connectivity, remyelination and oligodendrogenesis. These findings are associated with improved functional recovery. This novel role for EVs presents a new perspective in the development of biologics for brain repair. Nature Publishing Group 2017-03-16 /pmc/articles/PMC5353554/ /pubmed/28300134 http://dx.doi.org/10.1038/srep44433 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Otero-Ortega, Laura
Laso-García, Fernando
Gómez-de Frutos, María del Carmen
Rodríguez-Frutos, Berta
Pascual-Guerra, Jorge
Fuentes, Blanca
Díez-Tejedor, Exuperio
Gutiérrez-Fernández, María
White Matter Repair After Extracellular Vesicles Administration in an Experimental Animal Model of Subcortical Stroke
title White Matter Repair After Extracellular Vesicles Administration in an Experimental Animal Model of Subcortical Stroke
title_full White Matter Repair After Extracellular Vesicles Administration in an Experimental Animal Model of Subcortical Stroke
title_fullStr White Matter Repair After Extracellular Vesicles Administration in an Experimental Animal Model of Subcortical Stroke
title_full_unstemmed White Matter Repair After Extracellular Vesicles Administration in an Experimental Animal Model of Subcortical Stroke
title_short White Matter Repair After Extracellular Vesicles Administration in an Experimental Animal Model of Subcortical Stroke
title_sort white matter repair after extracellular vesicles administration in an experimental animal model of subcortical stroke
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5353554/
https://www.ncbi.nlm.nih.gov/pubmed/28300134
http://dx.doi.org/10.1038/srep44433
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