Neural Regeneration Research ›› 2015, Vol. 10 ›› Issue (11): 1799-1808.doi: 10.4103/1673-5374.170302

Previous Articles     Next Articles

MicroRNAs: a novel promising therapeutic target for cerebral ischemia/reperfusion injury?

Xiao-li Min1, 2, Ting-yong Wang3, Yi Cao4, Jia Liu1, Jin-tao Li1, #, Ting-hua Wang1, * , #   

  1. 1 Institute of Neuroscience, Kunming Medical University, Kunming, Yunnan Province, China
    2 Faculty of Clinical Medicine, Yunnan University of Traditional Chinese Medicine; the First Affiliated Hospital of Yunnan University of Traditional Chinese Medicine, Kunming, Yunnan Province, China
    3 School of Economics of Sichuan University, Chengdu, Sichuan Province, China
    4 Department of Neurosurgery, the Second Affiliated Hospital of Kunming Medical University, Kunming, Yunnan Province, China
  • Received:2015-07-10 Online:2015-12-07 Published:2015-12-07
  • Contact: Ting-hua Wang, M.D., Ph.D.,tinghua_neuron@263.net.
  • Supported by:

    This work was supported by grants from the National Natural Science Foundation of China, No. 81271358; Yunnan Science Foundation of China, No. 2013FZ199.

Abstract:

To determine the molecular mechanism of cerebral ischemia/reperfusion injury, we examined the microRNA (miRNA) expression profile in rat cortex after focal cerebral ischemia/reperfusion
injury using miRNA microarrays and bioinformatic tools to systematically analyze Gene Ontology (GO) function classifications, as well as the signaling pathways of genes targeted by these differentially expressed miRNAs. Our results show significantly changed miRNA expression profiles in the reperfusion period after focal cerebral ischemia, with a total of 15 miRNAs up-regulated
and 44 miRNAs down-regulated. Target genes of these differentially expressed miRNAs were mainly involved in metabolic and cellular processes, which were identified as hub nodes of a miRNA-GO-network. The most correlated pathways included D-glutamine and D-glutamate metabolism, the renin-angiotensin system, peroxisomes, the PPAR signaling pathway, SNARE interactions in vesicular transport, and the calcium signaling pathway. Our study suggests that miRNAs play an important role in the pathological process of cerebral ischemia/reperfusion injury. Understanding miRNA expression and function may shed light on the molecular mechanism
of cerebral ischemia/reperfusion injury.

Key words: nerve regeneration, microRNA, therapeutic target, cerebral ischemia/reperfusion injury, miRNA expression profiles, bioinformatics analysis, Gene Ontology analysis, molecular mechanism, KEGG pathway, neural regeneration