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The P2X4 receptor is required for neuroprotection via ischemic preconditioning
Ischemic preconditioning (IPC), a procedure consisting of transient ischemia and subsequent reperfusion, provides ischemic tolerance against prolonged ischemia in the brain. Although the blood flow changes mediated by IPC are primarily perceived by vascular endothelial cells, the role of these cells...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4865734/ https://www.ncbi.nlm.nih.gov/pubmed/27173846 http://dx.doi.org/10.1038/srep25893 |
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author | Ozaki, Tomohiko Muramatsu, Rieko Sasai, Miwa Yamamoto, Masahiro Kubota, Yoshiaki Fujinaka, Toshiyuki Yoshimine, Toshiki Yamashita, Toshihide |
author_facet | Ozaki, Tomohiko Muramatsu, Rieko Sasai, Miwa Yamamoto, Masahiro Kubota, Yoshiaki Fujinaka, Toshiyuki Yoshimine, Toshiki Yamashita, Toshihide |
author_sort | Ozaki, Tomohiko |
collection | PubMed |
description | Ischemic preconditioning (IPC), a procedure consisting of transient ischemia and subsequent reperfusion, provides ischemic tolerance against prolonged ischemia in the brain. Although the blood flow changes mediated by IPC are primarily perceived by vascular endothelial cells, the role of these cells in ischemic tolerance has not been fully clarified. In this study, we found that the P2X4 receptor, which is abundantly expressed in vascular endothelial cells, is required for ischemic tolerance following middle artery occlusion (MCAO) in mice. Mechanistically, the P2X4 receptor was stimulated by fluid shear stress, which mimics reperfusion, thus promoting the increased expression of osteopontin, a neuroprotective molecule. Furthermore, we found that the intracerebroventricular administration of osteopontin was sufficient to exert a neuroprotective effect mediated by preconditioning-stimulated P2X4 receptor activation. These results demonstrate a novel mechanism whereby vascular endothelial cells are involved in ischemic tolerance. |
format | Online Article Text |
id | pubmed-4865734 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48657342016-05-23 The P2X4 receptor is required for neuroprotection via ischemic preconditioning Ozaki, Tomohiko Muramatsu, Rieko Sasai, Miwa Yamamoto, Masahiro Kubota, Yoshiaki Fujinaka, Toshiyuki Yoshimine, Toshiki Yamashita, Toshihide Sci Rep Article Ischemic preconditioning (IPC), a procedure consisting of transient ischemia and subsequent reperfusion, provides ischemic tolerance against prolonged ischemia in the brain. Although the blood flow changes mediated by IPC are primarily perceived by vascular endothelial cells, the role of these cells in ischemic tolerance has not been fully clarified. In this study, we found that the P2X4 receptor, which is abundantly expressed in vascular endothelial cells, is required for ischemic tolerance following middle artery occlusion (MCAO) in mice. Mechanistically, the P2X4 receptor was stimulated by fluid shear stress, which mimics reperfusion, thus promoting the increased expression of osteopontin, a neuroprotective molecule. Furthermore, we found that the intracerebroventricular administration of osteopontin was sufficient to exert a neuroprotective effect mediated by preconditioning-stimulated P2X4 receptor activation. These results demonstrate a novel mechanism whereby vascular endothelial cells are involved in ischemic tolerance. Nature Publishing Group 2016-05-13 /pmc/articles/PMC4865734/ /pubmed/27173846 http://dx.doi.org/10.1038/srep25893 Text en Copyright © 2016, Macmillan Publishers Limited 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 Ozaki, Tomohiko Muramatsu, Rieko Sasai, Miwa Yamamoto, Masahiro Kubota, Yoshiaki Fujinaka, Toshiyuki Yoshimine, Toshiki Yamashita, Toshihide The P2X4 receptor is required for neuroprotection via ischemic preconditioning |
title | The P2X4 receptor is required for neuroprotection via ischemic preconditioning |
title_full | The P2X4 receptor is required for neuroprotection via ischemic preconditioning |
title_fullStr | The P2X4 receptor is required for neuroprotection via ischemic preconditioning |
title_full_unstemmed | The P2X4 receptor is required for neuroprotection via ischemic preconditioning |
title_short | The P2X4 receptor is required for neuroprotection via ischemic preconditioning |
title_sort | p2x4 receptor is required for neuroprotection via ischemic preconditioning |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4865734/ https://www.ncbi.nlm.nih.gov/pubmed/27173846 http://dx.doi.org/10.1038/srep25893 |
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