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Phosphorylation of leukocyte PECAM and its association with detergent-resistant membranes regulate transendothelial migration.白细胞 PECAM 的磷酸化及其与去污剂抗性膜的关联调节跨内皮迁移。
J Immunol. 2010 Aug 1;185(3):1878-86. doi: 10.4049/jimmunol.1001305. Epub 2010 Jun 25.
2
PECAM-1: conflicts of interest in inflammation.PECAM-1:炎症中的利益冲突。
Life Sci. 2010 Jul 17;87(3-4):69-82. doi: 10.1016/j.lfs.2010.06.001. Epub 2010 Jun 10.
3
A novel and critical role for tyrosine 663 in platelet endothelial cell adhesion molecule-1 trafficking and transendothelial migration.酪氨酸663在血小板内皮细胞黏附分子-1的转运和跨内皮迁移中具有全新且关键的作用。
J Immunol. 2009 Apr 15;182(8):5041-51. doi: 10.4049/jimmunol.0803192.
4
Vascular endothelium in atherosclerosis.动脉粥样硬化中的血管内皮
Cell Tissue Res. 2009 Jan;335(1):191-203. doi: 10.1007/s00441-008-0678-5. Epub 2008 Sep 17.
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Endothelial cell PECAM-1 promotes atherosclerotic lesions in areas of disturbed flow in ApoE-deficient mice.内皮细胞PECAM-1促进载脂蛋白E缺陷小鼠血流紊乱区域的动脉粥样硬化病变。
Arterioscler Thromb Vasc Biol. 2008 Nov;28(11):2003-8. doi: 10.1161/ATVBAHA.108.164707. Epub 2008 Aug 7.
6
Site-specific effects of PECAM-1 on atherosclerosis in LDL receptor-deficient mice.PECAM-1对低密度脂蛋白受体缺陷小鼠动脉粥样硬化的位点特异性作用。
Arterioscler Thromb Vasc Biol. 2008 Nov;28(11):1996-2002. doi: 10.1161/ATVBAHA.108.172270. Epub 2008 Jul 31.
7
Sphingosine 1-phosphate induces platelet/endothelial cell adhesion molecule-1 phosphorylation in human endothelial cells through cSrc and Fyn.鞘氨醇-1-磷酸通过cSrc和Fyn诱导人内皮细胞中血小板/内皮细胞黏附分子-1磷酸化。
Cell Signal. 2008 Aug;20(8):1521-7. doi: 10.1016/j.cellsig.2008.04.008. Epub 2008 Apr 18.
8
An alternatively spliced isoform of PECAM-1 is expressed at high levels in human and murine tissues, and suggests a novel role for the C-terminus of PECAM-1 in cytoprotective signaling.PECAM-1的一种可变剪接异构体在人和小鼠组织中高水平表达,提示PECAM-1的C末端在细胞保护信号传导中具有新作用。
J Cell Sci. 2008 Apr 15;121(Pt 8):1235-42. doi: 10.1242/jcs.025163.
9
Regulation of endothelial junctional permeability.内皮细胞连接通透性的调节。
Ann N Y Acad Sci. 2008 Mar;1123:134-45. doi: 10.1196/annals.1420.016.
10
PECAM-1 ligation negatively regulates TLR4 signaling in macrophages.血小板内皮细胞黏附分子-1(PECAM-1)的连接对巨噬细胞中Toll样受体4(TLR4)信号传导起负向调节作用。
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PECAM-1 黏附和信号在维持血管完整性中的相对贡献。

Relative contribution of PECAM-1 adhesion and signaling to the maintenance of vascular integrity.

机构信息

Blood Research Institute, Blood Center of Wisconsin, Milwaukee, WI 53201, USA.

出版信息

J Cell Sci. 2011 May 1;124(Pt 9):1477-85. doi: 10.1242/jcs.082271. Epub 2011 Apr 12.

DOI:10.1242/jcs.082271
PMID:21486942
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3078814/
Abstract

PECAM-1 (CD31) is a cellular adhesion and signaling receptor that is highly expressed at endothelial cell-cell junctions in confluent vascular beds. Previous studies have implicated PECAM-1 in the maintenance of vascular barrier integrity; however, the mechanisms behind PECAM-1-mediated barrier protection are still poorly understood. The goal of the present study, therefore, was to examine the pertinent biological properties of PECAM-1 (i.e. adhesion and/or signaling) that allow it to support barrier integrity. We found that, compared with PECAM-1-deficient endothelial cells, PECAM-1-expressing endothelial cell monolayers exhibit increased steady-state barrier function, as well as more rapid restoration of barrier integrity following thrombin-induced perturbation of the endothelial cell monolayer. The majority of PECAM-1-mediated barrier protection was found to be due to the ability of PECAM-1 to interact homophilically and become localized to cell-cell junctions, because a homophilic binding-crippled mutant form of PECAM-1 was unable to support efficient barrier function when re-expressed in cells. By contrast, cells expressing PECAM-1 variants lacking residues known to be involved in PECAM-1-mediated signal transduction exhibited normal to near-normal barrier integrity. Taken together, these studies suggest that PECAM-1-PECAM-1 homophilic interactions are more important than its signaling function for maintaining the integrity of endothelial cell junctions.

摘要

PECAM-1(CD31)是一种细胞黏附和信号受体,在血管腔中高表达于内皮细胞-细胞连接处。先前的研究表明 PECAM-1 参与维持血管屏障的完整性;然而,PECAM-1 介导的屏障保护的机制仍知之甚少。因此,本研究的目的是研究 PECAM-1(即黏附和/或信号)的相关生物学特性,使其能够支持屏障的完整性。我们发现,与 PECAM-1 缺陷型内皮细胞相比,表达 PECAM-1 的内皮细胞单层具有更高的稳态屏障功能,并且在凝血酶诱导的内皮细胞单层扰动后,屏障完整性的恢复更快。发现 PECAM-1 介导的大部分屏障保护归因于 PECAM-1 能够同型相互作用并定位到细胞-细胞连接处,因为同型结合失活突变体形式的 PECAM-1 无法在细胞中重新表达时支持有效的屏障功能。相比之下,表达缺乏已知参与 PECAM-1 介导的信号转导的残基的 PECAM-1 变体的细胞表现出正常或接近正常的屏障完整性。综上所述,这些研究表明,PECAM-1-PECAM-1 同型相互作用对于维持内皮细胞连接的完整性比其信号转导功能更为重要。