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A novel therapeutic approach using peripheral blood mononuclear cells preconditioned by oxygen-glucose deprivation
Cell therapies that invoke pleiotropic mechanisms may facilitate functional recovery in patients with stroke. Based on previous experiments using microglia preconditioned by oxygen-glucose deprivation, we hypothesized that the administration of peripheral blood mononuclear cells (PBMCs) precondition...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6856386/ https://www.ncbi.nlm.nih.gov/pubmed/31728010 http://dx.doi.org/10.1038/s41598-019-53418-5 |
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author | Hatakeyama, Masahiro Kanazawa, Masato Ninomiya, Itaru Omae, Kaoru Kimura, Yasuko Takahashi, Tetsuya Onodera, Osamu Fukushima, Masanori Shimohata, Takayoshi |
author_facet | Hatakeyama, Masahiro Kanazawa, Masato Ninomiya, Itaru Omae, Kaoru Kimura, Yasuko Takahashi, Tetsuya Onodera, Osamu Fukushima, Masanori Shimohata, Takayoshi |
author_sort | Hatakeyama, Masahiro |
collection | PubMed |
description | Cell therapies that invoke pleiotropic mechanisms may facilitate functional recovery in patients with stroke. Based on previous experiments using microglia preconditioned by oxygen-glucose deprivation, we hypothesized that the administration of peripheral blood mononuclear cells (PBMCs) preconditioned by oxygen-glucose deprivation (OGD-PBMCs) to be a therapeutic strategy for ischemic stroke. Here, OGD-PBMCs were identified to secrete remodelling factors, including the vascular endothelial growth factor and transforming growth factor-β in vitro, while intra-arterial administration of OGD-PBMCs at 7 days after focal cerebral ischemia prompted expression of such factors in the brain parenchyma at 28 days following focal cerebral ischemia in vivo. Furthermore, administration of OGD-PBMCs induced an increasing number of stage-specific embryonic antigen-3-positive cells both in vitro and in vivo. Finally, it was found to prompt angiogenesis and axonal outgrowth, and functional recovery after cerebral ischemia. In conclusion, the administration of OGD-PBMCs might be a novel therapeutic strategy against ischemic stroke. |
format | Online Article Text |
id | pubmed-6856386 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-68563862019-12-17 A novel therapeutic approach using peripheral blood mononuclear cells preconditioned by oxygen-glucose deprivation Hatakeyama, Masahiro Kanazawa, Masato Ninomiya, Itaru Omae, Kaoru Kimura, Yasuko Takahashi, Tetsuya Onodera, Osamu Fukushima, Masanori Shimohata, Takayoshi Sci Rep Article Cell therapies that invoke pleiotropic mechanisms may facilitate functional recovery in patients with stroke. Based on previous experiments using microglia preconditioned by oxygen-glucose deprivation, we hypothesized that the administration of peripheral blood mononuclear cells (PBMCs) preconditioned by oxygen-glucose deprivation (OGD-PBMCs) to be a therapeutic strategy for ischemic stroke. Here, OGD-PBMCs were identified to secrete remodelling factors, including the vascular endothelial growth factor and transforming growth factor-β in vitro, while intra-arterial administration of OGD-PBMCs at 7 days after focal cerebral ischemia prompted expression of such factors in the brain parenchyma at 28 days following focal cerebral ischemia in vivo. Furthermore, administration of OGD-PBMCs induced an increasing number of stage-specific embryonic antigen-3-positive cells both in vitro and in vivo. Finally, it was found to prompt angiogenesis and axonal outgrowth, and functional recovery after cerebral ischemia. In conclusion, the administration of OGD-PBMCs might be a novel therapeutic strategy against ischemic stroke. Nature Publishing Group UK 2019-11-14 /pmc/articles/PMC6856386/ /pubmed/31728010 http://dx.doi.org/10.1038/s41598-019-53418-5 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Hatakeyama, Masahiro Kanazawa, Masato Ninomiya, Itaru Omae, Kaoru Kimura, Yasuko Takahashi, Tetsuya Onodera, Osamu Fukushima, Masanori Shimohata, Takayoshi A novel therapeutic approach using peripheral blood mononuclear cells preconditioned by oxygen-glucose deprivation |
title | A novel therapeutic approach using peripheral blood mononuclear cells preconditioned by oxygen-glucose deprivation |
title_full | A novel therapeutic approach using peripheral blood mononuclear cells preconditioned by oxygen-glucose deprivation |
title_fullStr | A novel therapeutic approach using peripheral blood mononuclear cells preconditioned by oxygen-glucose deprivation |
title_full_unstemmed | A novel therapeutic approach using peripheral blood mononuclear cells preconditioned by oxygen-glucose deprivation |
title_short | A novel therapeutic approach using peripheral blood mononuclear cells preconditioned by oxygen-glucose deprivation |
title_sort | novel therapeutic approach using peripheral blood mononuclear cells preconditioned by oxygen-glucose deprivation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6856386/ https://www.ncbi.nlm.nih.gov/pubmed/31728010 http://dx.doi.org/10.1038/s41598-019-53418-5 |
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