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Human placental mesenchymal stem cells improve stroke outcomes via extracellular vesicles-mediated preservation of cerebral blood flow
BACKGROUND: Besides long-term trans-differentiation into neural cells, benefits of stem cell therapy (SCT) in ischemic stroke may include secretion of protective factors, which partly reflects extracellular vesicle (EVs) released by stem cell. However, the mechanism(s) by which stem cells/EVs limit...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7753936/ https://www.ncbi.nlm.nih.gov/pubmed/33348090 http://dx.doi.org/10.1016/j.ebiom.2020.103161 |
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author | Barzegar, Mansoureh Wang, Yuping Eshaq, Randa S. Yun, J. Winny Boyer, Christen J. Cananzi, Sergio G. White, Luke A. Chernyshev, Oleg Kelley, Roger E. Minagar, Alireza Stokes, Karen Y. Lu, Xiao-Hong Alexander, Jonathan S. |
author_facet | Barzegar, Mansoureh Wang, Yuping Eshaq, Randa S. Yun, J. Winny Boyer, Christen J. Cananzi, Sergio G. White, Luke A. Chernyshev, Oleg Kelley, Roger E. Minagar, Alireza Stokes, Karen Y. Lu, Xiao-Hong Alexander, Jonathan S. |
author_sort | Barzegar, Mansoureh |
collection | PubMed |
description | BACKGROUND: Besides long-term trans-differentiation into neural cells, benefits of stem cell therapy (SCT) in ischemic stroke may include secretion of protective factors, which partly reflects extracellular vesicle (EVs) released by stem cell. However, the mechanism(s) by which stem cells/EVs limit stroke injury have yet to be fully defined. METHODS: We evaluated the protection effect of human placenta mesenchymal stem cells (hPMSC) as a potential form of SCT in experimental ischemic stroke ‘transient middle cerebral artery occusion (MCAO)/reperfusion’ mice model. FINDINGS: We found for the first time that intraperitoneal administration of hPMSCs or intravenous hPMSC-derived EVs, given at the time of reperfusion, significantly protected the ipsilateral hemisphere from ischemic injury. This protection was associated with significant restoration of normal blood flow to the post-MCAO brain. More importantly, EVs derived from hPMSC promote paracrine-based protection of SCT in the MCAO model in a cholesterol/lipid-dependent manner. INTERPRETATION: Together, our results demonstrated beneficial effects of hPMSC/EVs in experimental stroke models which could permit the rapid “translation” of these cells into clinical trials in the near-term. |
format | Online Article Text |
id | pubmed-7753936 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-77539362020-12-23 Human placental mesenchymal stem cells improve stroke outcomes via extracellular vesicles-mediated preservation of cerebral blood flow Barzegar, Mansoureh Wang, Yuping Eshaq, Randa S. Yun, J. Winny Boyer, Christen J. Cananzi, Sergio G. White, Luke A. Chernyshev, Oleg Kelley, Roger E. Minagar, Alireza Stokes, Karen Y. Lu, Xiao-Hong Alexander, Jonathan S. EBioMedicine Research Paper BACKGROUND: Besides long-term trans-differentiation into neural cells, benefits of stem cell therapy (SCT) in ischemic stroke may include secretion of protective factors, which partly reflects extracellular vesicle (EVs) released by stem cell. However, the mechanism(s) by which stem cells/EVs limit stroke injury have yet to be fully defined. METHODS: We evaluated the protection effect of human placenta mesenchymal stem cells (hPMSC) as a potential form of SCT in experimental ischemic stroke ‘transient middle cerebral artery occusion (MCAO)/reperfusion’ mice model. FINDINGS: We found for the first time that intraperitoneal administration of hPMSCs or intravenous hPMSC-derived EVs, given at the time of reperfusion, significantly protected the ipsilateral hemisphere from ischemic injury. This protection was associated with significant restoration of normal blood flow to the post-MCAO brain. More importantly, EVs derived from hPMSC promote paracrine-based protection of SCT in the MCAO model in a cholesterol/lipid-dependent manner. INTERPRETATION: Together, our results demonstrated beneficial effects of hPMSC/EVs in experimental stroke models which could permit the rapid “translation” of these cells into clinical trials in the near-term. Elsevier 2020-12-19 /pmc/articles/PMC7753936/ /pubmed/33348090 http://dx.doi.org/10.1016/j.ebiom.2020.103161 Text en © 2020 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Research Paper Barzegar, Mansoureh Wang, Yuping Eshaq, Randa S. Yun, J. Winny Boyer, Christen J. Cananzi, Sergio G. White, Luke A. Chernyshev, Oleg Kelley, Roger E. Minagar, Alireza Stokes, Karen Y. Lu, Xiao-Hong Alexander, Jonathan S. Human placental mesenchymal stem cells improve stroke outcomes via extracellular vesicles-mediated preservation of cerebral blood flow |
title | Human placental mesenchymal stem cells improve stroke outcomes via extracellular vesicles-mediated preservation of cerebral blood flow |
title_full | Human placental mesenchymal stem cells improve stroke outcomes via extracellular vesicles-mediated preservation of cerebral blood flow |
title_fullStr | Human placental mesenchymal stem cells improve stroke outcomes via extracellular vesicles-mediated preservation of cerebral blood flow |
title_full_unstemmed | Human placental mesenchymal stem cells improve stroke outcomes via extracellular vesicles-mediated preservation of cerebral blood flow |
title_short | Human placental mesenchymal stem cells improve stroke outcomes via extracellular vesicles-mediated preservation of cerebral blood flow |
title_sort | human placental mesenchymal stem cells improve stroke outcomes via extracellular vesicles-mediated preservation of cerebral blood flow |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7753936/ https://www.ncbi.nlm.nih.gov/pubmed/33348090 http://dx.doi.org/10.1016/j.ebiom.2020.103161 |
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