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Analysis of miRNAs Involved in Mouse Brain Damage upon Enterovirus 71 Infection
Enterovirus 71 (EV71) infects the central nervous system (CNS) and causes brainstem encephalitis in children. MiRNAs have been found to play various functions in EV71 infection in human cell lines. To identify potential miRNAs involved in the inflammatory injury in CNS, our study, for the first time...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5395563/ https://www.ncbi.nlm.nih.gov/pubmed/28469998 http://dx.doi.org/10.3389/fcimb.2017.00133 |
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author | Yang, Xiaoxia Xie, Jing Jia, Leili Liu, Nan Liang, Yuan Wu, Fuli Liang, Beibei Li, Yongrui Wang, Jinyan Sheng, Chunyu Li, Hao Liu, Hongbo Ma, Qiuxia Yang, Chaojie Du, Xinying Qiu, Shaofu Song, Hongbin |
author_facet | Yang, Xiaoxia Xie, Jing Jia, Leili Liu, Nan Liang, Yuan Wu, Fuli Liang, Beibei Li, Yongrui Wang, Jinyan Sheng, Chunyu Li, Hao Liu, Hongbo Ma, Qiuxia Yang, Chaojie Du, Xinying Qiu, Shaofu Song, Hongbin |
author_sort | Yang, Xiaoxia |
collection | PubMed |
description | Enterovirus 71 (EV71) infects the central nervous system (CNS) and causes brainstem encephalitis in children. MiRNAs have been found to play various functions in EV71 infection in human cell lines. To identify potential miRNAs involved in the inflammatory injury in CNS, our study, for the first time, performed a miRNA microarray assay in vivo using EV71 infected mice brains. Twenty differentially expressed miRNAs were identified (four up- and 16 down-regulated) and confirmed by qRT-PCR. The target genes of these miRNAs were analyzed using KEGG (Kyoto Encyclopedia of Genes and Genomes) analysis, revealing that the miRNAs were mainly involved in the regulation of inflammation and neural system function. MiR-150-5p, -3082-5p, -3473a, -468-3p, -669n, -721, -709, and -5107-5p that regulate MAPK and chemokine signaling were all down-regulated, which might result in increased cytokine production. In addition, miR-3473a could also regulate focal adhesion and leukocyte trans-endothelial migration, suggesting a role in virus-induced blood-brain barrier disruption. The miRNAs and pathways identified in this study could help to understand the intricate interactions between EV71 and the brain injury, offering new insight for the future research of the molecular mechanism of EV71 induced brainstem encephalitis. |
format | Online Article Text |
id | pubmed-5395563 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53955632017-05-03 Analysis of miRNAs Involved in Mouse Brain Damage upon Enterovirus 71 Infection Yang, Xiaoxia Xie, Jing Jia, Leili Liu, Nan Liang, Yuan Wu, Fuli Liang, Beibei Li, Yongrui Wang, Jinyan Sheng, Chunyu Li, Hao Liu, Hongbo Ma, Qiuxia Yang, Chaojie Du, Xinying Qiu, Shaofu Song, Hongbin Front Cell Infect Microbiol Microbiology Enterovirus 71 (EV71) infects the central nervous system (CNS) and causes brainstem encephalitis in children. MiRNAs have been found to play various functions in EV71 infection in human cell lines. To identify potential miRNAs involved in the inflammatory injury in CNS, our study, for the first time, performed a miRNA microarray assay in vivo using EV71 infected mice brains. Twenty differentially expressed miRNAs were identified (four up- and 16 down-regulated) and confirmed by qRT-PCR. The target genes of these miRNAs were analyzed using KEGG (Kyoto Encyclopedia of Genes and Genomes) analysis, revealing that the miRNAs were mainly involved in the regulation of inflammation and neural system function. MiR-150-5p, -3082-5p, -3473a, -468-3p, -669n, -721, -709, and -5107-5p that regulate MAPK and chemokine signaling were all down-regulated, which might result in increased cytokine production. In addition, miR-3473a could also regulate focal adhesion and leukocyte trans-endothelial migration, suggesting a role in virus-induced blood-brain barrier disruption. The miRNAs and pathways identified in this study could help to understand the intricate interactions between EV71 and the brain injury, offering new insight for the future research of the molecular mechanism of EV71 induced brainstem encephalitis. Frontiers Media S.A. 2017-04-19 /pmc/articles/PMC5395563/ /pubmed/28469998 http://dx.doi.org/10.3389/fcimb.2017.00133 Text en Copyright © 2017 Yang, Xie, Jia, Liu, Liang, Wu, Liang, Li, Wang, Sheng, Li, Liu, Ma, Yang, Du, Qiu and Song. 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 | Microbiology Yang, Xiaoxia Xie, Jing Jia, Leili Liu, Nan Liang, Yuan Wu, Fuli Liang, Beibei Li, Yongrui Wang, Jinyan Sheng, Chunyu Li, Hao Liu, Hongbo Ma, Qiuxia Yang, Chaojie Du, Xinying Qiu, Shaofu Song, Hongbin Analysis of miRNAs Involved in Mouse Brain Damage upon Enterovirus 71 Infection |
title | Analysis of miRNAs Involved in Mouse Brain Damage upon Enterovirus 71 Infection |
title_full | Analysis of miRNAs Involved in Mouse Brain Damage upon Enterovirus 71 Infection |
title_fullStr | Analysis of miRNAs Involved in Mouse Brain Damage upon Enterovirus 71 Infection |
title_full_unstemmed | Analysis of miRNAs Involved in Mouse Brain Damage upon Enterovirus 71 Infection |
title_short | Analysis of miRNAs Involved in Mouse Brain Damage upon Enterovirus 71 Infection |
title_sort | analysis of mirnas involved in mouse brain damage upon enterovirus 71 infection |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5395563/ https://www.ncbi.nlm.nih.gov/pubmed/28469998 http://dx.doi.org/10.3389/fcimb.2017.00133 |
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