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Global MicroRNA Expression Profiling of Mouse Livers following Ischemia-Reperfusion Injury at Different Stages
Hepatic ischemia-reperfusion injury is a dynamic process consisting of two stages: ischemia and reperfusion, and triggers a cascade of physiological and biochemical events. Given the important role of microRNAs in regulating gene expression, we analyzed gene expression changes in mouse livers at sha...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4747576/ https://www.ncbi.nlm.nih.gov/pubmed/26859886 http://dx.doi.org/10.1371/journal.pone.0148677 |
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author | Zheng, Weisheng Men, Hewei Li, Jing Xing, Yu Wu, Bin Wang, Zhenglu Li, Junjie Teng, Dahong Shi, Yuan Li, Jiang Jiang, Pu Cai, Jinzhen |
author_facet | Zheng, Weisheng Men, Hewei Li, Jing Xing, Yu Wu, Bin Wang, Zhenglu Li, Junjie Teng, Dahong Shi, Yuan Li, Jiang Jiang, Pu Cai, Jinzhen |
author_sort | Zheng, Weisheng |
collection | PubMed |
description | Hepatic ischemia-reperfusion injury is a dynamic process consisting of two stages: ischemia and reperfusion, and triggers a cascade of physiological and biochemical events. Given the important role of microRNAs in regulating gene expression, we analyzed gene expression changes in mouse livers at sham control, ischemia stage, and reperfusion stage. We generated global expression profiles of microRNA and mRNA genes in mouse livers subjected to ischemia-reperfusion injury at the three stages, respectively. Comparison analysis showed that reperfusion injury had a distinct expression profile whereas the ischemia sample and the sham control were clustered together. Consistently, there are 69 differentially expressed microRNAs between the reperfusion sample and the sham control whereas 28 differentially expressed microRNAs between the ischemia sample and the sham control. We further identified two modes of microRNA expression changes in ischemia-reperfusion injury. Functional analysis of both the differentially expressed microRNAs in the two modes and their target mRNAs revealed that ischemia injury impaired mitochondrial function, nutrient consumption, and metabolism process. In contrast, reperfusion injury led to severe tissue inflammation that is predominantly an innate-immune response in the ischemia-reperfusion process. Our staged analysis of gene expression profiles provides new insights into regulatory mechanisms of microRNAs in mouse hepatic IR injury. |
format | Online Article Text |
id | pubmed-4747576 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-47475762016-02-22 Global MicroRNA Expression Profiling of Mouse Livers following Ischemia-Reperfusion Injury at Different Stages Zheng, Weisheng Men, Hewei Li, Jing Xing, Yu Wu, Bin Wang, Zhenglu Li, Junjie Teng, Dahong Shi, Yuan Li, Jiang Jiang, Pu Cai, Jinzhen PLoS One Research Article Hepatic ischemia-reperfusion injury is a dynamic process consisting of two stages: ischemia and reperfusion, and triggers a cascade of physiological and biochemical events. Given the important role of microRNAs in regulating gene expression, we analyzed gene expression changes in mouse livers at sham control, ischemia stage, and reperfusion stage. We generated global expression profiles of microRNA and mRNA genes in mouse livers subjected to ischemia-reperfusion injury at the three stages, respectively. Comparison analysis showed that reperfusion injury had a distinct expression profile whereas the ischemia sample and the sham control were clustered together. Consistently, there are 69 differentially expressed microRNAs between the reperfusion sample and the sham control whereas 28 differentially expressed microRNAs between the ischemia sample and the sham control. We further identified two modes of microRNA expression changes in ischemia-reperfusion injury. Functional analysis of both the differentially expressed microRNAs in the two modes and their target mRNAs revealed that ischemia injury impaired mitochondrial function, nutrient consumption, and metabolism process. In contrast, reperfusion injury led to severe tissue inflammation that is predominantly an innate-immune response in the ischemia-reperfusion process. Our staged analysis of gene expression profiles provides new insights into regulatory mechanisms of microRNAs in mouse hepatic IR injury. Public Library of Science 2016-02-09 /pmc/articles/PMC4747576/ /pubmed/26859886 http://dx.doi.org/10.1371/journal.pone.0148677 Text en © 2016 Zheng et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Zheng, Weisheng Men, Hewei Li, Jing Xing, Yu Wu, Bin Wang, Zhenglu Li, Junjie Teng, Dahong Shi, Yuan Li, Jiang Jiang, Pu Cai, Jinzhen Global MicroRNA Expression Profiling of Mouse Livers following Ischemia-Reperfusion Injury at Different Stages |
title | Global MicroRNA Expression Profiling of Mouse Livers following Ischemia-Reperfusion Injury at Different Stages |
title_full | Global MicroRNA Expression Profiling of Mouse Livers following Ischemia-Reperfusion Injury at Different Stages |
title_fullStr | Global MicroRNA Expression Profiling of Mouse Livers following Ischemia-Reperfusion Injury at Different Stages |
title_full_unstemmed | Global MicroRNA Expression Profiling of Mouse Livers following Ischemia-Reperfusion Injury at Different Stages |
title_short | Global MicroRNA Expression Profiling of Mouse Livers following Ischemia-Reperfusion Injury at Different Stages |
title_sort | global microrna expression profiling of mouse livers following ischemia-reperfusion injury at different stages |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4747576/ https://www.ncbi.nlm.nih.gov/pubmed/26859886 http://dx.doi.org/10.1371/journal.pone.0148677 |
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