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下调 microRNA-195 通过靶向 VEGFA 促进脑梗死诱导的血管生成。

Downregulation of microRNA-195 promotes angiogenesis induced by cerebral infarction via targeting VEGFA.

机构信息

Department of Neurology, The Affiliated Hospital of Hebei University of Engineering, Handan, Hebei 056002, P.R. China.

Handan Emergency Rescue Command Center, Handan, Hebei 056002, P.R. China.

出版信息

Mol Med Rep. 2017 Oct;16(4):5434-5440. doi: 10.3892/mmr.2017.7230. Epub 2017 Aug 11.

Abstract

Angiogenesis, the formation of new blood vessels from preexisting endothelium, is a process that involves a series of interassociated and mutually interactive pathophysiological processes. It is accepted that microRNAs (miRNAs) regulate endothelial cell behavior, including their involvement in angiogenesis. However, it remains unclear whether miRNAs are involved in the regulation of angiogenesis following cerebral ischemia. Therefore, the present study aimed to investigate the role of miRNAs in angiogenesis and the underlying mechanism following cerebral ischemia. Expression profiles of miRNAs in rat brain samples following middle cerebral artery occlusion (MCAO) were investigated using a miRNA microarray. The expression of candidate miRNA, miR‑195 was further validated using reverse transcription‑quantitative polymerase chain reaction. Then, the effects of miR‑195 on cell migration and tube formation of human umbilical vein vascular endothelial cells (HUVECs) were investigated following miR‑195 silencing, and overexpression. The specific target genes of miR‑195 were predicted using microRNA prediction bioinformatics software (http://www.microrna.org/microrna/home.do), and then confirmed using a dual‑luciferase reporter assay and rescue experiment. It was demonstrated that miR‑195 was significantly downregulated in the brains of rats following MCAO and in hypoxia‑induced HUVECs. Furthermore, it was revealed that miR‑195 overexpression inhibited the invasion ability and tube formation of HUVECs in vitro, while miR‑195 silencing enhanced these functions. In addition, vascular endothelial growth factor A (VEGFA) was identified as a direct target of miR‑195 and was negatively correlated with miR‑195 expression. In addition, the rescue experiment revealed that overexpression of VEGFA reversed the inhibitory effects of miR‑195 overexpression on the invasion ability and tube formation of HUVECs. The present study has provided a novel insight into the promoting roles of miR‑195 downregulation on angiogenesis following cerebral infarction and suggests that the miR‑195/VEGFA signaling pathway is a putative therapeutic target in cerebral ischemia.

摘要

血管生成是指从预先存在的内皮细胞形成新的血管,是一个涉及一系列相互关联和相互作用的病理生理过程。人们普遍认为 microRNAs(miRNAs)调节内皮细胞的行为,包括它们在血管生成中的参与。然而,miRNAs 是否参与脑缺血后血管生成的调节仍不清楚。因此,本研究旨在探讨 miRNAs 在脑缺血后血管生成中的作用及其潜在机制。通过 miRNA 微阵列研究大鼠脑样本在大脑中动脉闭塞(MCAO)后 miRNAs 的表达谱。使用逆转录定量聚合酶链反应进一步验证候选 miRNA,miR-195 的表达。然后,通过 miR-195 沉默和过表达研究 miR-195 对人脐静脉血管内皮细胞(HUVEC)的细胞迁移和管状形成的影响。使用 microRNA 预测生物信息学软件(http://www.microrna.org/microrna/home.do)预测 miR-195 的特异性靶基因,然后使用双荧光素酶报告基因检测和挽救实验进行验证。结果表明,MCAO 后大鼠脑和缺氧诱导的 HUVEC 中 miR-195 表达明显下调。此外,研究表明 miR-195 过表达抑制 HUVEC 在体外的侵袭能力和管状形成,而 miR-195 沉默增强了这些功能。此外,血管内皮生长因子 A(VEGFA)被鉴定为 miR-195 的直接靶基因,与 miR-195 表达呈负相关。此外,挽救实验表明,VEGFA 的过表达逆转了 miR-195 过表达对 HUVEC 侵袭能力和管状形成的抑制作用。本研究为脑梗死后 miR-195 下调促进血管生成提供了新的见解,并表明 miR-195/VEGFA 信号通路可能是脑缺血的潜在治疗靶点。

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