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Microglia preconditioned by oxygen-glucose deprivation promote functional recovery in ischemic rats
Cell-therapies that invoke pleiotropic mechanisms may facilitate functional recovery in stroke patients. We hypothesized that a cell therapy using microglia preconditioned by optimal oxygen-glucose deprivation (OGD) is a therapeutic strategy for ischemic stroke because optimal ischemia induces anti-...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5307390/ https://www.ncbi.nlm.nih.gov/pubmed/28195185 http://dx.doi.org/10.1038/srep42582 |
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author | Kanazawa, Masato Miura, Minami Toriyabe, Masafumi Koyama, Misaki Hatakeyama, Masahiro Ishikawa, Masanori Nakajima, Takashi Onodera, Osamu Takahashi, Tetsuya Nishizawa, Masatoyo Shimohata, Takayoshi |
author_facet | Kanazawa, Masato Miura, Minami Toriyabe, Masafumi Koyama, Misaki Hatakeyama, Masahiro Ishikawa, Masanori Nakajima, Takashi Onodera, Osamu Takahashi, Tetsuya Nishizawa, Masatoyo Shimohata, Takayoshi |
author_sort | Kanazawa, Masato |
collection | PubMed |
description | Cell-therapies that invoke pleiotropic mechanisms may facilitate functional recovery in stroke patients. We hypothesized that a cell therapy using microglia preconditioned by optimal oxygen-glucose deprivation (OGD) is a therapeutic strategy for ischemic stroke because optimal ischemia induces anti-inflammatory M2 microglia. We first delineated changes in angiogenesis and axonal outgrowth in the ischemic cortex using rats. We found that slight angiogenesis without axonal outgrowth were activated at the border area within the ischemic core from 7 to 14 days after ischemia. Next, we demonstrated that administration of primary microglia preconditioned by 18 hours of OGD at 7 days prompted functional recovery at 28 days after focal cerebral ischemia compared to control therapies by marked secretion of remodelling factors such as vascular endothelial growth factor, matrix metalloproteinase-9, and transforming growth factor-β polarized to M2 microglia in vitro/vivo. In conclusion, intravascular administration of M2 microglia preconditioned by optimal OGD may be a novel therapeutic strategy against ischemic stroke. |
format | Online Article Text |
id | pubmed-5307390 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53073902017-02-22 Microglia preconditioned by oxygen-glucose deprivation promote functional recovery in ischemic rats Kanazawa, Masato Miura, Minami Toriyabe, Masafumi Koyama, Misaki Hatakeyama, Masahiro Ishikawa, Masanori Nakajima, Takashi Onodera, Osamu Takahashi, Tetsuya Nishizawa, Masatoyo Shimohata, Takayoshi Sci Rep Article Cell-therapies that invoke pleiotropic mechanisms may facilitate functional recovery in stroke patients. We hypothesized that a cell therapy using microglia preconditioned by optimal oxygen-glucose deprivation (OGD) is a therapeutic strategy for ischemic stroke because optimal ischemia induces anti-inflammatory M2 microglia. We first delineated changes in angiogenesis and axonal outgrowth in the ischemic cortex using rats. We found that slight angiogenesis without axonal outgrowth were activated at the border area within the ischemic core from 7 to 14 days after ischemia. Next, we demonstrated that administration of primary microglia preconditioned by 18 hours of OGD at 7 days prompted functional recovery at 28 days after focal cerebral ischemia compared to control therapies by marked secretion of remodelling factors such as vascular endothelial growth factor, matrix metalloproteinase-9, and transforming growth factor-β polarized to M2 microglia in vitro/vivo. In conclusion, intravascular administration of M2 microglia preconditioned by optimal OGD may be a novel therapeutic strategy against ischemic stroke. Nature Publishing Group 2017-02-14 /pmc/articles/PMC5307390/ /pubmed/28195185 http://dx.doi.org/10.1038/srep42582 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 Kanazawa, Masato Miura, Minami Toriyabe, Masafumi Koyama, Misaki Hatakeyama, Masahiro Ishikawa, Masanori Nakajima, Takashi Onodera, Osamu Takahashi, Tetsuya Nishizawa, Masatoyo Shimohata, Takayoshi Microglia preconditioned by oxygen-glucose deprivation promote functional recovery in ischemic rats |
title | Microglia preconditioned by oxygen-glucose deprivation promote functional recovery in ischemic rats |
title_full | Microglia preconditioned by oxygen-glucose deprivation promote functional recovery in ischemic rats |
title_fullStr | Microglia preconditioned by oxygen-glucose deprivation promote functional recovery in ischemic rats |
title_full_unstemmed | Microglia preconditioned by oxygen-glucose deprivation promote functional recovery in ischemic rats |
title_short | Microglia preconditioned by oxygen-glucose deprivation promote functional recovery in ischemic rats |
title_sort | microglia preconditioned by oxygen-glucose deprivation promote functional recovery in ischemic rats |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5307390/ https://www.ncbi.nlm.nih.gov/pubmed/28195185 http://dx.doi.org/10.1038/srep42582 |
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