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DR-region of Na(+)/K(+) ATPase is a target to treat excitotoxicity and stroke
Na(+)/K(+) ATPase (NKA) is important in maintaining cellular functions. We found that loss of NKA activities in NKAα1(+/−) mice is associated with increased susceptibility to ischemic injuries following transient middle cerebral artery occlusion (tMCAO). This is corroborated by the neuroprotective e...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6315034/ https://www.ncbi.nlm.nih.gov/pubmed/30584244 http://dx.doi.org/10.1038/s41419-018-1230-5 |
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author | Shi, Meimei Cao, Lei Cao, Xu Zhu, Mengyuan Zhang, Xingzhou Wu, Zhiyuan Xiong, Siping Xie, Zhizhong Yang, Yong Chen, Jingyu Wong, Peter T. H. Bian, Jin-Song |
author_facet | Shi, Meimei Cao, Lei Cao, Xu Zhu, Mengyuan Zhang, Xingzhou Wu, Zhiyuan Xiong, Siping Xie, Zhizhong Yang, Yong Chen, Jingyu Wong, Peter T. H. Bian, Jin-Song |
author_sort | Shi, Meimei |
collection | PubMed |
description | Na(+)/K(+) ATPase (NKA) is important in maintaining cellular functions. We found that loss of NKA activities in NKAα1(+/−) mice is associated with increased susceptibility to ischemic injuries following transient middle cerebral artery occlusion (tMCAO). This is corroborated by the neuroprotective effects of an antibody raised against an extracellular DR region ((897)DVEDSYGQQWTYEQR(911), sequence number as in rat) of NKAα subunit (DR-Ab) in both preventive and therapeutic settings. DR-Ab protects cortical neurons against glutamate-induced toxicity by stimulating activities of NKA and Na(+)/Ca(2+) exchanger (NCX), which resulted in accelerated Ca(2+) extrusion. DR-Ab also enhanced the association between NKA and GluR2 and therefore reduced the internalization of both proteins from membrane induced by glutamate toxicity. The mechanism appears to involve suppression of GluR2 phosphorylation through PKCα/PICK pathway. Our data indicate that DR-region of NKA may be a novel therapeutic target for drug development for the treatment of ischemic stroke. |
format | Online Article Text |
id | pubmed-6315034 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63150342019-01-03 DR-region of Na(+)/K(+) ATPase is a target to treat excitotoxicity and stroke Shi, Meimei Cao, Lei Cao, Xu Zhu, Mengyuan Zhang, Xingzhou Wu, Zhiyuan Xiong, Siping Xie, Zhizhong Yang, Yong Chen, Jingyu Wong, Peter T. H. Bian, Jin-Song Cell Death Dis Article Na(+)/K(+) ATPase (NKA) is important in maintaining cellular functions. We found that loss of NKA activities in NKAα1(+/−) mice is associated with increased susceptibility to ischemic injuries following transient middle cerebral artery occlusion (tMCAO). This is corroborated by the neuroprotective effects of an antibody raised against an extracellular DR region ((897)DVEDSYGQQWTYEQR(911), sequence number as in rat) of NKAα subunit (DR-Ab) in both preventive and therapeutic settings. DR-Ab protects cortical neurons against glutamate-induced toxicity by stimulating activities of NKA and Na(+)/Ca(2+) exchanger (NCX), which resulted in accelerated Ca(2+) extrusion. DR-Ab also enhanced the association between NKA and GluR2 and therefore reduced the internalization of both proteins from membrane induced by glutamate toxicity. The mechanism appears to involve suppression of GluR2 phosphorylation through PKCα/PICK pathway. Our data indicate that DR-region of NKA may be a novel therapeutic target for drug development for the treatment of ischemic stroke. Nature Publishing Group UK 2018-12-18 /pmc/articles/PMC6315034/ /pubmed/30584244 http://dx.doi.org/10.1038/s41419-018-1230-5 Text en © The Author(s) 2018 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 Shi, Meimei Cao, Lei Cao, Xu Zhu, Mengyuan Zhang, Xingzhou Wu, Zhiyuan Xiong, Siping Xie, Zhizhong Yang, Yong Chen, Jingyu Wong, Peter T. H. Bian, Jin-Song DR-region of Na(+)/K(+) ATPase is a target to treat excitotoxicity and stroke |
title | DR-region of Na(+)/K(+) ATPase is a target to treat excitotoxicity and stroke |
title_full | DR-region of Na(+)/K(+) ATPase is a target to treat excitotoxicity and stroke |
title_fullStr | DR-region of Na(+)/K(+) ATPase is a target to treat excitotoxicity and stroke |
title_full_unstemmed | DR-region of Na(+)/K(+) ATPase is a target to treat excitotoxicity and stroke |
title_short | DR-region of Na(+)/K(+) ATPase is a target to treat excitotoxicity and stroke |
title_sort | dr-region of na(+)/k(+) atpase is a target to treat excitotoxicity and stroke |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6315034/ https://www.ncbi.nlm.nih.gov/pubmed/30584244 http://dx.doi.org/10.1038/s41419-018-1230-5 |
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