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次要组织相容性抗原 1(HMHA1)/ArhGAP45 是 RacGAP,也是内皮完整性的新型调节因子。

The minor histocompatibility antigen 1 (HMHA1)/ArhGAP45 is a RacGAP and a novel regulator of endothelial integrity.

机构信息

Department of Physiology, Institute for Cardiovascular Research, VU University Medical Center, Amsterdam, The Netherlands.

Department of Molecular Cytology, Swammerdam Institute for Life Sciences, van Leeuwenhoek Centre for Advanced Microscopy, University of Amsterdam, Amsterdam, The Netherlands.

出版信息

Vascul Pharmacol. 2018 Feb;101:38-47. doi: 10.1016/j.vph.2017.11.007. Epub 2017 Nov 21.

Abstract

Endothelial cells line the vasculature and act as gatekeepers that control the passage of plasma, macromolecules and cells from the circulation to the interstitial space. Dysfunction of the endothelial barrier can lead to uncontrolled leak or edema. Vascular leakage is a hallmark of a range of diseases and despite its large impact no specialized therapies are available to prevent or reduce it. RhoGTPases are known key regulators of cellular behavior that are directly involved in the regulation of the endothelial barrier. We recently performed a comprehensive analysis of the effect of all RhoGTPases and their regulators on basal endothelial integrity. In addition to novel positive regulators of endothelial barrier function, we also identified novel negative regulators, of which the ArhGAP45 (also known as HMHA1) was the most significant. We now demonstrate that ArhGAP45 acts as a Rac-GAP (GTPase-Activating Protein) in endothelial cells, which explains its negative effect on endothelial barrier function. Silencing ArhGAP45 not only promotes basal endothelial barrier function, but also increases cellular surface area and induces sprout formation in a 3D-fibrin matrix. Our data further shows that loss of ArhGAP45 promotes migration and shear stress adaptation. In conclusion, we identify ArhGAP45 (HMHA1) as a novel regulator, which contributes to the fine-tuning of the regulation of basal endothelial integrity.

摘要

内皮细胞排列在脉管系统中,充当控制从循环系统到细胞间隙的血浆、大分子和细胞通过的守门员。内皮屏障功能障碍可导致不受控制的渗漏或水肿。血管渗漏是一系列疾病的标志,尽管它的影响很大,但目前还没有专门的治疗方法来预防或减少它。RhoGTPases 是已知的细胞行为的关键调节剂,它们直接参与内皮屏障的调节。我们最近对所有 RhoGTPases 及其调节剂对基础内皮完整性的影响进行了全面分析。除了发现新的内皮屏障功能的正调控因子外,我们还鉴定了新的负调控因子,其中 ArhGAP45(也称为 HMHA1)是最重要的。我们现在证明 ArhGAP45 在血管内皮细胞中作为 Rac-GAP(GTPase-Activating Protein)发挥作用,这解释了它对内皮屏障功能的负效应。沉默 ArhGAP45 不仅促进了基础内皮屏障功能,还增加了细胞表面积,并在 3D 纤维蛋白基质中诱导芽形成。我们的数据进一步表明,ArhGAP45 的缺失促进了迁移和切应力适应。总之,我们确定 ArhGAP45(HMHA1)作为一种新的调节剂,有助于精细调节基础内皮完整性的调节。

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