MiR-375 attenuates injury of cerebral ischemia/reperfusion via targetting Ctgf
Author(s) -
Jianying Ou,
Li Kou,
Lingyan Liang,
Chaogang Tang
Publication year - 2017
Publication title -
bioscience reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.938
H-Index - 77
eISSN - 1573-4935
pISSN - 0144-8463
DOI - 10.1042/bsr20171242
Subject(s) - ctgf , microrna , ischemia , pi3k/akt/mtor pathway , pathogenesis , stroke (engine) , apoptosis , reperfusion injury , protein kinase b , medicine , mechanism (biology) , neuroprotection , neuroscience , signal transduction , in vivo , cerebral infarction , microbiology and biotechnology , biology , pharmacology , pathology , growth factor , gene , receptor , genetics , physics , quantum mechanics , thermodynamics
Ischemic stroke is the leading cause of disability and deaths worldwide. MiRNAs have been shown to play an important role in development and pathogenesis of the nervous system. However, the precise function and mechanism of miRNAs are not fully understood in the brain injury induced by ischemia/reperfusion (I/R). Herein, our study showed that miR-375 expression was significantly down-regulated in the rat I/R brain. With the in vivo and in vitro I/R stroke models, we found that miR-375 mimic provides significant protection from injury to cerebral I/R, which is reflected by reduced infarct volumes and cell apoptosis, and increased proliferation and migration of PC12 cells. Mechanistically, our findings showed that miR-375 binds to 3'-UTR region of Ctgf mRNA, subsequently leading to the decreased expression of Ctgf in the I/R brain. Furthermore, we showed that miR-375 /Ctgf-mediated protective effects are associated with p21/PI3K/Akt signaling pathways. Our findings thus provide a new insight into the mechanism of cerebral I/R injury and pave a potential new way for the therapy of cerebral I/R injury.
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