Dynamic Changes in miR-126 Expression in the Hippocampus and Penumbra Following Experimental Transient Global and Focal Cerebral Ischemia-Reperfusion

被引:20
|
作者
Xiao, Zhang Hong [1 ]
Wang, Li [2 ]
Gan, Ping [1 ]
He, Jing [1 ]
Yan, Bing Chun [2 ]
Ding, Li Dong [1 ]
机构
[1] Taizhou Second Peoples Hosp, Dept Neurol, Taizhou 225500, Peoples R China
[2] Yangzhou Univ, Affiliated Hosp, Dept Neurol, Jiangsu Key Lab Integrated Tradit Chinese & Weste, Yangzhou 225001, Jiangsu, Peoples R China
基金
中国博士后科学基金;
关键词
Cerebral ischemia; miR-126; Vascular; VEGFA; SPRED1; raf-1 signaling pathway; Neuronal damage; PROMOTES ANGIOGENESIS; NEURONAL DAMAGE; BRAIN; VEGF; MICRORNAS; INJURY; CELLS; NEUROGENESIS; GROWTH; MOUSE;
D O I
10.1007/s11064-020-02986-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
miR-126 which is considered one of the most important miRNAs for maintaining vascular integrity, plays an important role in neuroprotection after cerebral ischemia-reperfusion (I-R). Moreover, vascular endothelial growth factor A (VEGFA), sprouty-related EVH1 domain-containing protein 1 (SPRED1), and Raf-1 are also involved in physiological processes of vascular endothelial cells (ECs). This study investigated how miR-126 changes with reperfusion time in different brain tissues after global cerebral ischemia and focal cerebral ischemia and examined the underlying mechanism miR-126 involving VEGFA, SPRED1, and Raf-1 after I-R. The results indicated decreases in the levels of miR-126-3p and miR-126-5p expression in mice and gerbils after I-R, consistent with the results after oxygen and glucose deprivation and reperfusion (OGD/R) in PC12 cells. Glial cells were activated as neuronal damage gradually increased after I-R. Inhibition of miR-126-3p exacerbated the OGD/R-induced cell death and reduced cell viability. After miR-126-3p inhibition, the levels of SPRED1 and VEGFA expression were increased, and p-Raf-1 expression was decreased after OGD/R. Moreover, based on the intervention of miR-126-3p inhibition, we found that the expression of p-Raf-1 was significantly increased after the intervention of siSPRED1, while it was not statistically significant after intervention of siVEGFA. The reduction of miR-126 expression after global and focal cerebral ischemia exacerbated neuronal death, which was closely related to increasing the SPRED1 activation and inhibiting the Raf-1 expression.
引用
收藏
页码:1107 / 1119
页数:13
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