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YAP 通过抑制 STAT3/VEGF 信号促进血管内皮屏障修复。

YAP promotes endothelial barrier repair by repressing STAT3/VEGF signaling.

机构信息

Institute of Hypoxia Medicine, School of Basic Medical Sciences, Wenzhou Medical University, Wenzhou, Zhejiang, China.

Institute of Hypoxia Medicine, School of Basic Medical Sciences, Wenzhou Medical University, Wenzhou, Zhejiang, China.

出版信息

Life Sci. 2020 Sep 1;256:117884. doi: 10.1016/j.lfs.2020.117884. Epub 2020 Jun 2.

Abstract

AIMS

Endothelial barrier dysfunction is associated with multiple diseases, and barrier repair may be a possible therapeutic target. Yes-associated protein and its pathway have been implicated in organ repair after injury. However, the mechanisms underlying barrier repair and any role YAP plays in the process are unclear. This study aimed to explore the role and mechanism of YAP in the repair of endothelial cell permeability after TNF-α-induced injury.

MAIN METHODS

A trans-endothelial electrical resistance assay was performed to investigate changes in endothelial cell permeability. Lentivirus packaging by calcium phosphate transfection was used to construct endothelial cell lines with knocked down or overexpressed YAP. Western blotting, immunofluorescence, CO-IP, and real-time PCR were used to detect related protein and gene expression.

KEY FINDINGS

YAP is involved in the repair process of TNF-α-induced endothelial cell permeability injury; its overexpression promotes repair of endothelial cell permeability, and knockdown weakens repair ability. Moreover, YAP may promote repair by down-regulating STAT3 activity, thereby inhibiting VEGF expression.

SIGNIFICANCE

Elucidating the role of YAP in endothelial cell permeability repair process after injury might reveal mechanisms of endothelial barrier repair and provide therapeutic targets for treatment of vascular hyper-permeability disease.

摘要

目的

内皮细胞屏障功能障碍与多种疾病有关,而屏障修复可能是一种可行的治疗靶点。Yes 相关蛋白及其通路已被牵涉到损伤后器官修复。然而,目前尚不清楚屏障修复的机制以及 YAP 在该过程中所起的作用。本研究旨在探讨 YAP 在 TNF-α诱导的内皮细胞通透性损伤后的修复中的作用及其机制。

主要方法

通过跨内皮电阻抗测定法来研究内皮细胞通透性的变化。采用磷酸钙转染的慢病毒包装构建 YAP 敲低或过表达的内皮细胞系。通过 Western blot、免疫荧光、CO-IP 和实时 PCR 检测相关蛋白和基因的表达。

主要发现

YAP 参与 TNF-α诱导的内皮细胞通透性损伤的修复过程;其过表达促进内皮细胞通透性的修复,而敲低则削弱修复能力。此外,YAP 可能通过下调 STAT3 活性来促进修复,从而抑制 VEGF 的表达。

意义

阐明 YAP 在损伤后内皮细胞通透性修复过程中的作用,可能揭示内皮屏障修复的机制,并为治疗血管高通透性疾病提供治疗靶点。

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