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Brain immune cell composition and functional outcome after cerebral ischemia: comparison of two mouse strains
Inflammatory cells may contribute to secondary brain injury following cerebral ischemia. The C57Bl/6 mouse strain is known to exhibit a T helper 1-prone, pro-inflammatory type response to injury, whereas the FVB strain is relatively T helper 2-prone, or anti-inflammatory, in its immune response. We...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4237143/ https://www.ncbi.nlm.nih.gov/pubmed/25477780 http://dx.doi.org/10.3389/fncel.2014.00365 |
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author | Kim, Hyun Ah Whittle, Stephanie C. Lee, Seyoung Chu, Hannah X. Zhang, Shenpeng R. Wei, Zihui Arumugam, Thiruma V. Vinh, Anthony Drummond, Grant R. Sobey, Christopher G. |
author_facet | Kim, Hyun Ah Whittle, Stephanie C. Lee, Seyoung Chu, Hannah X. Zhang, Shenpeng R. Wei, Zihui Arumugam, Thiruma V. Vinh, Anthony Drummond, Grant R. Sobey, Christopher G. |
author_sort | Kim, Hyun Ah |
collection | PubMed |
description | Inflammatory cells may contribute to secondary brain injury following cerebral ischemia. The C57Bl/6 mouse strain is known to exhibit a T helper 1-prone, pro-inflammatory type response to injury, whereas the FVB strain is relatively T helper 2-prone, or anti-inflammatory, in its immune response. We tested whether stroke outcome is more severe in C57Bl/6 than FVB mice. Male mice of each strain underwent sham surgery or 1 h occlusion of the middle cerebral artery followed by 23 h of reperfusion. Despite no difference in infarct size, C57Bl/6 mice displayed markedly greater functional deficits than FVB mice after stroke, as assessed by neurological scoring and hanging wire test. Total numbers of CD45(+) leukocytes tended to be larger in the brains of C57Bl/6 than FVB mice after stroke, but there were marked differences in leukocyte composition between the two mouse strains. The inflammatory response in C57Bl/6 mice primarily involved T and B lymphocytes, whereas neutrophils, monocytes and macrophages were more prominent in FVB mice. Our data are consistent with the concept that functional outcome after stroke is dependent on the immune cell composition which develops following ischemic brain injury. |
format | Online Article Text |
id | pubmed-4237143 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-42371432014-12-04 Brain immune cell composition and functional outcome after cerebral ischemia: comparison of two mouse strains Kim, Hyun Ah Whittle, Stephanie C. Lee, Seyoung Chu, Hannah X. Zhang, Shenpeng R. Wei, Zihui Arumugam, Thiruma V. Vinh, Anthony Drummond, Grant R. Sobey, Christopher G. Front Cell Neurosci Neuroscience Inflammatory cells may contribute to secondary brain injury following cerebral ischemia. The C57Bl/6 mouse strain is known to exhibit a T helper 1-prone, pro-inflammatory type response to injury, whereas the FVB strain is relatively T helper 2-prone, or anti-inflammatory, in its immune response. We tested whether stroke outcome is more severe in C57Bl/6 than FVB mice. Male mice of each strain underwent sham surgery or 1 h occlusion of the middle cerebral artery followed by 23 h of reperfusion. Despite no difference in infarct size, C57Bl/6 mice displayed markedly greater functional deficits than FVB mice after stroke, as assessed by neurological scoring and hanging wire test. Total numbers of CD45(+) leukocytes tended to be larger in the brains of C57Bl/6 than FVB mice after stroke, but there were marked differences in leukocyte composition between the two mouse strains. The inflammatory response in C57Bl/6 mice primarily involved T and B lymphocytes, whereas neutrophils, monocytes and macrophages were more prominent in FVB mice. Our data are consistent with the concept that functional outcome after stroke is dependent on the immune cell composition which develops following ischemic brain injury. Frontiers Media S.A. 2014-11-19 /pmc/articles/PMC4237143/ /pubmed/25477780 http://dx.doi.org/10.3389/fncel.2014.00365 Text en Copyright © 2014 Kim, Whittle, Lee, Chu, Zhang, Wei, Arumugam, Vinh, Drummond and Sobey. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Kim, Hyun Ah Whittle, Stephanie C. Lee, Seyoung Chu, Hannah X. Zhang, Shenpeng R. Wei, Zihui Arumugam, Thiruma V. Vinh, Anthony Drummond, Grant R. Sobey, Christopher G. Brain immune cell composition and functional outcome after cerebral ischemia: comparison of two mouse strains |
title | Brain immune cell composition and functional outcome after cerebral ischemia: comparison of two mouse strains |
title_full | Brain immune cell composition and functional outcome after cerebral ischemia: comparison of two mouse strains |
title_fullStr | Brain immune cell composition and functional outcome after cerebral ischemia: comparison of two mouse strains |
title_full_unstemmed | Brain immune cell composition and functional outcome after cerebral ischemia: comparison of two mouse strains |
title_short | Brain immune cell composition and functional outcome after cerebral ischemia: comparison of two mouse strains |
title_sort | brain immune cell composition and functional outcome after cerebral ischemia: comparison of two mouse strains |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4237143/ https://www.ncbi.nlm.nih.gov/pubmed/25477780 http://dx.doi.org/10.3389/fncel.2014.00365 |
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