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...

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Main Authors: Weisheng Zheng, Hewei Men, Jing Li, Yu Xing, Bin Wu, Zhenglu Wang, Junjie Li, Dahong Teng, Yuan Shi, Jiang Li, Pu Jiang, Jinzhen Cai
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2016-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4747576?pdf=render
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author Weisheng Zheng
Hewei Men
Jing Li
Yu Xing
Bin Wu
Zhenglu Wang
Junjie Li
Dahong Teng
Yuan Shi
Jiang Li
Pu Jiang
Jinzhen Cai
author_facet Weisheng Zheng
Hewei Men
Jing Li
Yu Xing
Bin Wu
Zhenglu Wang
Junjie Li
Dahong Teng
Yuan Shi
Jiang Li
Pu Jiang
Jinzhen Cai
author_sort Weisheng Zheng
collection DOAJ
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.
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spelling doaj.art-1017fd12a7ad4258b78d18f4665b7d232022-12-22T01:57:59ZengPublic Library of Science (PLoS)PLoS ONE1932-62032016-01-01112e014867710.1371/journal.pone.0148677Global MicroRNA Expression Profiling of Mouse Livers following Ischemia-Reperfusion Injury at Different Stages.Weisheng ZhengHewei MenJing LiYu XingBin WuZhenglu WangJunjie LiDahong TengYuan ShiJiang LiPu JiangJinzhen CaiHepatic 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.http://europepmc.org/articles/PMC4747576?pdf=render
spellingShingle Weisheng Zheng
Hewei Men
Jing Li
Yu Xing
Bin Wu
Zhenglu Wang
Junjie Li
Dahong Teng
Yuan Shi
Jiang Li
Pu Jiang
Jinzhen Cai
Global MicroRNA Expression Profiling of Mouse Livers following Ischemia-Reperfusion Injury at Different Stages.
PLoS ONE
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
url http://europepmc.org/articles/PMC4747576?pdf=render
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