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Functional Recovery Caused by Human Adipose Tissue Mesenchymal Stem Cell-Derived Extracellular Vesicles Administered 24 h after Stroke in Rats
Ischemic stroke is a major cause of death and disability, intensely demanding innovative and accessible therapeutic strategies. Approaches presenting a prolonged period for therapeutic intervention and new treatment administration routes are promising tools for stroke treatment. Here, we evaluated t...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8657917/ https://www.ncbi.nlm.nih.gov/pubmed/34884665 http://dx.doi.org/10.3390/ijms222312860 |
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author | Rohden, Francieli Teixeira, Luciele Varaschini Bernardi, Luis Pedro Ferreira, Pamela Cristina Lukasewicz Colombo, Mariana Teixeira, Geciele Rodrigues de Oliveira, Fernanda dos Santos Cirne Lima, Elizabeth Obino Guma, Fátima Costa Rodrigues Souza, Diogo Onofre |
author_facet | Rohden, Francieli Teixeira, Luciele Varaschini Bernardi, Luis Pedro Ferreira, Pamela Cristina Lukasewicz Colombo, Mariana Teixeira, Geciele Rodrigues de Oliveira, Fernanda dos Santos Cirne Lima, Elizabeth Obino Guma, Fátima Costa Rodrigues Souza, Diogo Onofre |
author_sort | Rohden, Francieli |
collection | PubMed |
description | Ischemic stroke is a major cause of death and disability, intensely demanding innovative and accessible therapeutic strategies. Approaches presenting a prolonged period for therapeutic intervention and new treatment administration routes are promising tools for stroke treatment. Here, we evaluated the potential neuroprotective properties of nasally administered human adipose tissue mesenchymal stem cell (hAT-MSC)-derived extracellular vesicles (EVs) obtained from healthy individuals who underwent liposuction. After a single intranasal EV (200 µg/kg) administered 24 h after a focal permanent ischemic stroke in rats, a higher number of EVs, improvement of the blood–brain barrier, and re-stabilization of vascularization were observed in the recoverable peri-infarct zone, as well as a significant decrease in infarct volume. In addition, EV treatment recovered long-term motor (front paws symmetry) and behavioral impairment (short- and long-term memory and anxiety-like behavior) induced by ischemic stroke. In line with these findings, our work highlights hAT-MSC-derived EVs as a promising therapeutic strategy for stroke. |
format | Online Article Text |
id | pubmed-8657917 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-86579172021-12-10 Functional Recovery Caused by Human Adipose Tissue Mesenchymal Stem Cell-Derived Extracellular Vesicles Administered 24 h after Stroke in Rats Rohden, Francieli Teixeira, Luciele Varaschini Bernardi, Luis Pedro Ferreira, Pamela Cristina Lukasewicz Colombo, Mariana Teixeira, Geciele Rodrigues de Oliveira, Fernanda dos Santos Cirne Lima, Elizabeth Obino Guma, Fátima Costa Rodrigues Souza, Diogo Onofre Int J Mol Sci Article Ischemic stroke is a major cause of death and disability, intensely demanding innovative and accessible therapeutic strategies. Approaches presenting a prolonged period for therapeutic intervention and new treatment administration routes are promising tools for stroke treatment. Here, we evaluated the potential neuroprotective properties of nasally administered human adipose tissue mesenchymal stem cell (hAT-MSC)-derived extracellular vesicles (EVs) obtained from healthy individuals who underwent liposuction. After a single intranasal EV (200 µg/kg) administered 24 h after a focal permanent ischemic stroke in rats, a higher number of EVs, improvement of the blood–brain barrier, and re-stabilization of vascularization were observed in the recoverable peri-infarct zone, as well as a significant decrease in infarct volume. In addition, EV treatment recovered long-term motor (front paws symmetry) and behavioral impairment (short- and long-term memory and anxiety-like behavior) induced by ischemic stroke. In line with these findings, our work highlights hAT-MSC-derived EVs as a promising therapeutic strategy for stroke. MDPI 2021-11-28 /pmc/articles/PMC8657917/ /pubmed/34884665 http://dx.doi.org/10.3390/ijms222312860 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Rohden, Francieli Teixeira, Luciele Varaschini Bernardi, Luis Pedro Ferreira, Pamela Cristina Lukasewicz Colombo, Mariana Teixeira, Geciele Rodrigues de Oliveira, Fernanda dos Santos Cirne Lima, Elizabeth Obino Guma, Fátima Costa Rodrigues Souza, Diogo Onofre Functional Recovery Caused by Human Adipose Tissue Mesenchymal Stem Cell-Derived Extracellular Vesicles Administered 24 h after Stroke in Rats |
title | Functional Recovery Caused by Human Adipose Tissue Mesenchymal Stem Cell-Derived Extracellular Vesicles Administered 24 h after Stroke in Rats |
title_full | Functional Recovery Caused by Human Adipose Tissue Mesenchymal Stem Cell-Derived Extracellular Vesicles Administered 24 h after Stroke in Rats |
title_fullStr | Functional Recovery Caused by Human Adipose Tissue Mesenchymal Stem Cell-Derived Extracellular Vesicles Administered 24 h after Stroke in Rats |
title_full_unstemmed | Functional Recovery Caused by Human Adipose Tissue Mesenchymal Stem Cell-Derived Extracellular Vesicles Administered 24 h after Stroke in Rats |
title_short | Functional Recovery Caused by Human Adipose Tissue Mesenchymal Stem Cell-Derived Extracellular Vesicles Administered 24 h after Stroke in Rats |
title_sort | functional recovery caused by human adipose tissue mesenchymal stem cell-derived extracellular vesicles administered 24 h after stroke in rats |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8657917/ https://www.ncbi.nlm.nih.gov/pubmed/34884665 http://dx.doi.org/10.3390/ijms222312860 |
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