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TRPC6 is the endothelial calcium channel that regulates leukocyte transendothelial migration during the inflammatory response.瞬时受体电位通道6(TRPC6)是一种内皮钙通道,在炎症反应过程中调节白细胞跨内皮迁移。
J Exp Med. 2015 Oct 19;212(11):1883-99. doi: 10.1084/jem.20150353. Epub 2015 Sep 21.
2
Endothelial CD99 signals through soluble adenylyl cyclase and PKA to regulate leukocyte transendothelial migration.内皮细胞CD99通过可溶性腺苷酸环化酶和蛋白激酶A发出信号,以调节白细胞跨内皮迁移。
J Exp Med. 2015 Jun 29;212(7):1021-41. doi: 10.1084/jem.20150354. Epub 2015 Jun 22.
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The regulation of transendothelial migration: new knowledge and new questions.跨内皮迁移的调控:新知识与新问题
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How endothelial cells regulate transmigration of leukocytes in the inflammatory response.内皮细胞如何调节炎症反应中白细胞的迁移。
Am J Pathol. 2014 Apr;184(4):886-96. doi: 10.1016/j.ajpath.2013.12.033.
5
CD47 plays a critical role in T-cell recruitment by regulation of LFA-1 and VLA-4 integrin adhesive functions.CD47 在 T 细胞募集中发挥关键作用,通过调节 LFA-1 和 VLA-4 整合素黏附功能。
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Nat Methods. 2012 Jul;9(7):671-5. doi: 10.1038/nmeth.2089.
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Pericytes support neutrophil subendothelial cell crawling and breaching of venular walls in vivo.周细胞支持中性粒细胞在内皮细胞下的爬行和活体静脉壁的突破。
J Exp Med. 2012 Jun 4;209(6):1219-34. doi: 10.1084/jem.20111622. Epub 2012 May 21.
8
The junctional adhesion molecule JAM-C regulates polarized transendothelial migration of neutrophils in vivo.连接黏附分子 JAM-C 调控体内中性粒细胞的极化跨内皮迁移。
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9
Leukocyte rolling and adhesion both contribute to regulation of microvascular permeability to albumin via ligation of ICAM-1.白细胞滚动和黏附均通过 ICAM-1 的连接作用有助于调节白蛋白通过微血管的通透性。
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Mechanisms of leukocyte transendothelial migration.白细胞跨内皮迁移的机制。
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四维活体显微镜揭示了PECAM和CD99在白细胞渗出过程中作用的关键应变差异。

4D intravital microscopy uncovers critical strain differences for the roles of PECAM and CD99 in leukocyte diapedesis.

作者信息

Sullivan David P, Watson Richard L, Muller William A

机构信息

Department of Pathology, Feinberg School of Medicine, Chicago, Illinois.

Department of Pathology, Feinberg School of Medicine, Chicago, Illinois

出版信息

Am J Physiol Heart Circ Physiol. 2016 Sep 1;311(3):H621-32. doi: 10.1152/ajpheart.00289.2016. Epub 2016 Jul 15.

DOI:10.1152/ajpheart.00289.2016
PMID:27422987
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5142183/
Abstract

Leukocyte transendothelial migration (TEM) is an essential component of the inflammatory response. In vitro studies with human cells have demonstrated that platelet/endothelial cell adhesion molecule (PECAM) functions upstream of CD99 during TEM; however, results in vivo with mice have been apparently contradictory. In this study we use four-dimensional (4D) intravital microscopy to demonstrate that the site and order of function of PECAM and CD99 in vivo are dependent on the strain of mice. In FVB/n mice, PECAM functions upstream of CD99, as in human cells in vitro, and blocking antibodies against either molecule arrest neutrophils before they traverse the endothelium. However, in C57BL/6 mice, PECAM and CD99 appear to function at a different step, as the same antibodies arrest leukocyte migration through the endothelial basement membrane. These results are the first direct comparison of PECAM and CD99 function in different murine strains as well as the first demonstration of the sequential function of PECAM and CD99 in vivo.

摘要

白细胞跨内皮迁移(TEM)是炎症反应的一个重要组成部分。对人类细胞的体外研究表明,在TEM过程中血小板/内皮细胞黏附分子(PECAM)在CD99的上游发挥作用;然而,在小鼠体内的研究结果显然相互矛盾。在本研究中,我们使用四维(4D)活体显微镜来证明体内PECAM和CD99的功能位点和顺序取决于小鼠品系。在FVB/n小鼠中,PECAM在CD99的上游发挥作用,就像在体外人类细胞中一样,针对这两种分子的阻断抗体在中性粒细胞穿过内皮之前就会阻止它们。然而,在C57BL/6小鼠中,PECAM和CD99似乎在不同步骤发挥作用,因为相同的抗体可阻止白细胞穿过内皮基底膜。这些结果首次直接比较了不同小鼠品系中PECAM和CD99的功能,也是首次证明体内PECAM和CD99的顺序功能。