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Differential gene expression in the contralateral hemisphere of the rat brain after focal ischemia

Ischemic stroke is one of the most severe polygenic brain diseases. Here, we performed further functional genetic analysis of the processes occurring in the contralateral hemisphere (CH) after ischemia–reperfusion injury in rat brain. Comparison of RNA sequencing data for subcortical samples from th...

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Autores principales: Filippenkov, Ivan B., Remizova, Julia A., Denisova, Alina E., Stavchansky, Vasily V., Golovina, Ksenia D., Gubsky, Leonid V., Limborska, Svetlana A., Dergunova, Lyudmila V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9834327/
https://www.ncbi.nlm.nih.gov/pubmed/36631528
http://dx.doi.org/10.1038/s41598-023-27663-8
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author Filippenkov, Ivan B.
Remizova, Julia A.
Denisova, Alina E.
Stavchansky, Vasily V.
Golovina, Ksenia D.
Gubsky, Leonid V.
Limborska, Svetlana A.
Dergunova, Lyudmila V.
author_facet Filippenkov, Ivan B.
Remizova, Julia A.
Denisova, Alina E.
Stavchansky, Vasily V.
Golovina, Ksenia D.
Gubsky, Leonid V.
Limborska, Svetlana A.
Dergunova, Lyudmila V.
author_sort Filippenkov, Ivan B.
collection PubMed
description Ischemic stroke is one of the most severe polygenic brain diseases. Here, we performed further functional genetic analysis of the processes occurring in the contralateral hemisphere (CH) after ischemia–reperfusion injury in rat brain. Comparison of RNA sequencing data for subcortical samples from the ipsilateral hemisphere (IH) and CH after 90 min of transient middle cerebral artery occlusion (tMCAO) and corresponding sham-operated (SO) controls showed four groups of genes that were associated with ischemic processes in rat brain at 24 h after tMCAO. Among them, 2672 genes were differentially expressed genes (DEGs) for IH but non-DEGs for CH, 34 genes were DEGs for CH but non-DEGs for IH, and 114 genes had codirected changes in expression in both hemispheres. The remaining 16 genes exhibited opposite changes at the mRNA level in the two brain hemispheres after tMCAO. These findings suggest that the ischemic process caused by a focal ischemia induces complex bilateral reactions at the transcriptome level in the rat brain. We believe that specific genome responses in the CH and IH may provide a useful model for the study of the potential for brain repair after stroke.
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spelling pubmed-98343272023-01-13 Differential gene expression in the contralateral hemisphere of the rat brain after focal ischemia Filippenkov, Ivan B. Remizova, Julia A. Denisova, Alina E. Stavchansky, Vasily V. Golovina, Ksenia D. Gubsky, Leonid V. Limborska, Svetlana A. Dergunova, Lyudmila V. Sci Rep Article Ischemic stroke is one of the most severe polygenic brain diseases. Here, we performed further functional genetic analysis of the processes occurring in the contralateral hemisphere (CH) after ischemia–reperfusion injury in rat brain. Comparison of RNA sequencing data for subcortical samples from the ipsilateral hemisphere (IH) and CH after 90 min of transient middle cerebral artery occlusion (tMCAO) and corresponding sham-operated (SO) controls showed four groups of genes that were associated with ischemic processes in rat brain at 24 h after tMCAO. Among them, 2672 genes were differentially expressed genes (DEGs) for IH but non-DEGs for CH, 34 genes were DEGs for CH but non-DEGs for IH, and 114 genes had codirected changes in expression in both hemispheres. The remaining 16 genes exhibited opposite changes at the mRNA level in the two brain hemispheres after tMCAO. These findings suggest that the ischemic process caused by a focal ischemia induces complex bilateral reactions at the transcriptome level in the rat brain. We believe that specific genome responses in the CH and IH may provide a useful model for the study of the potential for brain repair after stroke. Nature Publishing Group UK 2023-01-11 /pmc/articles/PMC9834327/ /pubmed/36631528 http://dx.doi.org/10.1038/s41598-023-27663-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Filippenkov, Ivan B.
Remizova, Julia A.
Denisova, Alina E.
Stavchansky, Vasily V.
Golovina, Ksenia D.
Gubsky, Leonid V.
Limborska, Svetlana A.
Dergunova, Lyudmila V.
Differential gene expression in the contralateral hemisphere of the rat brain after focal ischemia
title Differential gene expression in the contralateral hemisphere of the rat brain after focal ischemia
title_full Differential gene expression in the contralateral hemisphere of the rat brain after focal ischemia
title_fullStr Differential gene expression in the contralateral hemisphere of the rat brain after focal ischemia
title_full_unstemmed Differential gene expression in the contralateral hemisphere of the rat brain after focal ischemia
title_short Differential gene expression in the contralateral hemisphere of the rat brain after focal ischemia
title_sort differential gene expression in the contralateral hemisphere of the rat brain after focal ischemia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9834327/
https://www.ncbi.nlm.nih.gov/pubmed/36631528
http://dx.doi.org/10.1038/s41598-023-27663-8
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