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血管内皮(VE)钙黏蛋白、内皮细胞黏附连接和血管疾病。

Vascular Endothelial (VE)-Cadherin, Endothelial Adherens Junctions, and Vascular Disease.

机构信息

Fondazione Italiana per la Ricerca sul Cancro (FIRC) Institute of Molecular Oncology, 20139 Milan, Italy.

Mario Negri Institute for Pharmacological Research, 20156 Milan, Italy.

出版信息

Cold Spring Harb Perspect Biol. 2018 Oct 1;10(10):a029322. doi: 10.1101/cshperspect.a029322.

DOI:10.1101/cshperspect.a029322
PMID:28851747
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6169812/
Abstract

Endothelial cell-cell adherens junctions (AJs) supervise fundamental vascular functions, such as the control of permeability and transmigration of circulating leukocytes, and the maintenance of existing vessels and formation of new ones. These processes are often dysregulated in pathologies. However, the evidence that links dysfunction of endothelial AJs to human pathologies is mostly correlative. In this review, we present an update of the molecular organization of AJ complexes in endothelial cells (ECs) that is mainly based on observations from experimental models. Furthermore, we report in detail on a human pathology, cerebral cavernous malformation (CCM), which is initiated by loss-of-function mutations in the genes that encode the three cytoplasmic components of AJs (CCM1, CCM2, and CCM3). At present, these represent a unique example of mutations in components of endothelial AJs that cause human disease. We describe also how studies into the defects of AJs in CCM are shedding light on the crucial regulatory mechanisms and signaling activities of these endothelial structures. Although these observations are specific for CCM, they support the concept that dysfunction of endothelial AJs can directly contribute to human pathologies.

摘要

内皮细胞-细胞黏附连接(AJs)调控着基本的血管功能,如对循环白细胞的通透性和迁移的控制,以及现有血管的维持和新血管的形成。这些过程在病理状态下常常失调。然而,将内皮 AJs 功能障碍与人类疾病联系起来的证据大多是相关性的。在这篇综述中,我们主要基于实验模型的观察,介绍了内皮细胞(ECs)中 AJ 复合物的分子组织的最新进展。此外,我们详细报告了一种人类病理学,即脑海绵状血管畸形(CCM),它是由编码 AJ 三个细胞质成分(CCM1、CCM2 和 CCM3)的基因突变引起的。目前,这些代表了内皮 AJ 成分突变导致人类疾病的独特范例。我们还描述了 CCM 中 AJ 缺陷的研究如何揭示了这些内皮结构的关键调节机制和信号活性。尽管这些观察结果是 CCM 特有的,但它们支持了内皮 AJs 功能障碍可能直接导致人类疾病的概念。

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J Biol Chem. 2017 Feb 3;292(5):1884-1898. doi: 10.1074/jbc.M116.762393. Epub 2016 Dec 21.
2
RhoA Kinase Inhibition With Fasudil Versus Simvastatin in Murine Models of Cerebral Cavernous Malformations.在脑海绵状血管畸形小鼠模型中,法舒地尔与辛伐他汀对RhoA激酶的抑制作用比较
Stroke. 2017 Jan;48(1):187-194. doi: 10.1161/STROKEAHA.116.015013. Epub 2016 Nov 22.
3
Transendothelial migration: unifying principles from the endothelial perspective.跨内皮迁移:从内皮细胞角度看统一的原理
Immunol Rev. 2016 Sep;273(1):61-75. doi: 10.1111/imr.12443.
4
Endothelial exocytosis of angiopoietin-2 resulting from CCM3 deficiency contributes to cerebral cavernous malformation.CCM3缺乏导致的血管生成素-2内皮细胞胞吐作用促成脑海绵状血管畸形。
Nat Med. 2016 Sep;22(9):1033-1042. doi: 10.1038/nm.4169. Epub 2016 Aug 22.
5
Cell-cell junctional mechanotransduction in endothelial remodeling.内皮重塑中的细胞间连接机械转导
Cell Mol Life Sci. 2017 Jan;74(2):279-292. doi: 10.1007/s00018-016-2325-8. Epub 2016 Aug 9.
6
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Sci Signal. 2016 Jul 19;9(437):ra72. doi: 10.1126/scisignal.aad9256.
7
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Elife. 2016 May 24;5:e14847. doi: 10.7554/eLife.14847.
8
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Nature. 2016 Apr 7;532(7597):122-6. doi: 10.1038/nature17178. Epub 2016 Mar 30.
9
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Nat Commun. 2016 Mar 23;7:11017. doi: 10.1038/ncomms11017.
10
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Circ Res. 2016 Mar 4;118(5):881-97. doi: 10.1161/CIRCRESAHA.115.306529.