Let-7i attenuates human brain microvascular endothelial cell damage in oxygen glucose deprivation model by decreasing toll-like receptor 4 expression

被引:28
作者
Xiang, Wei [1 ,3 ]
Tian, Canhui [1 ]
Peng, Shunli [2 ]
Zhou, Liang [1 ]
Pan, Suyue [1 ]
Deng, Zhen [1 ]
机构
[1] Southern Med Univ, Nanfang Hosp, Dept Neurol, Guangzhou, Guangdong, Peoples R China
[2] Southern Med Univ, Nanfang Hosp, Dept Radiat Oncol, Guangzhou, Guangdong, Peoples R China
[3] Guangzhou Militray Command, Dept Neurol, Guangzhou Gen Hosp, Guangzhou, Guangdong, Peoples R China
关键词
Oxygen glucose deprivation (OGD); Human brain microvascular endothelial cell (HBMEC); Let-7i; Toll-like receptor 4 (TLR4); MICRORNA; BARRIER;
D O I
10.1016/j.bbrc.2017.08.093
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
The let-7 family of microRNAs (miRNAs) plays an important role on endothelial cell function. However, there have been few studies on their role under ischemic conditions. In this study, we demonstrate that let-7i, belonging to the let-7 family, rescues human brain microvascular endothelial cells (HBMECs) in an oxygen-glucose deprivation (OGD) model. Our data show that the expression of let-7 family miRNAs was downregulated after OGD. Overexpression of let-7i significantly alleviated cell death and improved survival of OGD-treated HBMECs. Let-7i also protected permeability in an in vitro blood brain barrier (BBB) model. Further, let-7i downregulated the expression of toll-like receptor 4 (TLR4), an inflammation trigger. Moreover, overexpression of let-7i decreased matrix metallopeptidase 9 (MMP9) and inducible nitric oxide synthase (iNOS) expression under OGD. Upon silencing TLR4 expression in HBMECs, the anti-inflammatory effect of let-7i was abolished. Our research suggests that let-7i promotes OGD-induced inflammation via downregulating TLR4 expression. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:788 / 793
页数:6
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