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Expression of miRNAs and Their Cooperative Regulation of the Pathophysiology in Traumatic Brain Injury
Traumatic brain injury (TBI) is a leading cause of injury-related death and disability worldwide. Effective treatment for TBI is limited and many TBI patients suffer from neuropsychiatric sequelae. The molecular and cellular mechanisms underlying the neuronal damage and impairment of mental abilitie...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3382215/ https://www.ncbi.nlm.nih.gov/pubmed/22761770 http://dx.doi.org/10.1371/journal.pone.0039357 |
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author | Hu, Zhonghua Yu, Danni Almeida-Suhett, Camila Tu, Kang Marini, Ann M. Eiden, Lee Braga, Maria F. Zhu, Jun Li, Zheng |
author_facet | Hu, Zhonghua Yu, Danni Almeida-Suhett, Camila Tu, Kang Marini, Ann M. Eiden, Lee Braga, Maria F. Zhu, Jun Li, Zheng |
author_sort | Hu, Zhonghua |
collection | PubMed |
description | Traumatic brain injury (TBI) is a leading cause of injury-related death and disability worldwide. Effective treatment for TBI is limited and many TBI patients suffer from neuropsychiatric sequelae. The molecular and cellular mechanisms underlying the neuronal damage and impairment of mental abilities following TBI are largely unknown. Here we used the next generation sequencing platform to delineate miRNA transcriptome changes in the hippocampus at 24 hours and 7 days following TBI in the rat controlled cortical impact injury (CCI) model, and developed a bioinformatic analysis to identify cellular activities that are regulated by miRNAs differentially expressed in the CCI brains. The results of our study indicate that distinct sets of miRNAs are regulated at different post-traumatic times, and suggest that multiple miRNA species cooperatively regulate cellular pathways for the pathological changes and management of brain injury. The distinctive miRNAs expression profiles at different post-CCI times may be used as molecular signatures to assess TBI progression. In addition to known pathophysiological changes, our study identifies many other cellular pathways that are subjected to modification by differentially expressed miRNAs in TBI brains. These pathways can potentially be targeted for development of novel TBI treatment. |
format | Online Article Text |
id | pubmed-3382215 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-33822152012-07-03 Expression of miRNAs and Their Cooperative Regulation of the Pathophysiology in Traumatic Brain Injury Hu, Zhonghua Yu, Danni Almeida-Suhett, Camila Tu, Kang Marini, Ann M. Eiden, Lee Braga, Maria F. Zhu, Jun Li, Zheng PLoS One Research Article Traumatic brain injury (TBI) is a leading cause of injury-related death and disability worldwide. Effective treatment for TBI is limited and many TBI patients suffer from neuropsychiatric sequelae. The molecular and cellular mechanisms underlying the neuronal damage and impairment of mental abilities following TBI are largely unknown. Here we used the next generation sequencing platform to delineate miRNA transcriptome changes in the hippocampus at 24 hours and 7 days following TBI in the rat controlled cortical impact injury (CCI) model, and developed a bioinformatic analysis to identify cellular activities that are regulated by miRNAs differentially expressed in the CCI brains. The results of our study indicate that distinct sets of miRNAs are regulated at different post-traumatic times, and suggest that multiple miRNA species cooperatively regulate cellular pathways for the pathological changes and management of brain injury. The distinctive miRNAs expression profiles at different post-CCI times may be used as molecular signatures to assess TBI progression. In addition to known pathophysiological changes, our study identifies many other cellular pathways that are subjected to modification by differentially expressed miRNAs in TBI brains. These pathways can potentially be targeted for development of novel TBI treatment. Public Library of Science 2012-06-22 /pmc/articles/PMC3382215/ /pubmed/22761770 http://dx.doi.org/10.1371/journal.pone.0039357 Text en This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication. https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. |
spellingShingle | Research Article Hu, Zhonghua Yu, Danni Almeida-Suhett, Camila Tu, Kang Marini, Ann M. Eiden, Lee Braga, Maria F. Zhu, Jun Li, Zheng Expression of miRNAs and Their Cooperative Regulation of the Pathophysiology in Traumatic Brain Injury |
title | Expression of miRNAs and Their Cooperative Regulation of the Pathophysiology in Traumatic Brain Injury |
title_full | Expression of miRNAs and Their Cooperative Regulation of the Pathophysiology in Traumatic Brain Injury |
title_fullStr | Expression of miRNAs and Their Cooperative Regulation of the Pathophysiology in Traumatic Brain Injury |
title_full_unstemmed | Expression of miRNAs and Their Cooperative Regulation of the Pathophysiology in Traumatic Brain Injury |
title_short | Expression of miRNAs and Their Cooperative Regulation of the Pathophysiology in Traumatic Brain Injury |
title_sort | expression of mirnas and their cooperative regulation of the pathophysiology in traumatic brain injury |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3382215/ https://www.ncbi.nlm.nih.gov/pubmed/22761770 http://dx.doi.org/10.1371/journal.pone.0039357 |
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