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2
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本文引用的文献

1
Segregation of VE-cadherin from the LBRC depends on the ectodomain sequence required for homophilic adhesion.血管内皮钙黏蛋白与低密度脂蛋白受体相关蛋白复合物的分离取决于同源性黏附所需的胞外域序列。
J Cell Sci. 2015 Feb 1;128(3):576-88. doi: 10.1242/jcs.159053.
2
Rapid remodeling of tight junctions during paracellular diapedesis in a human model of the blood-brain barrier.在血脑屏障的人类模型中,细胞旁渗出过程中紧密连接的快速重塑。
J Immunol. 2014 Sep 1;193(5):2427-37. doi: 10.4049/jimmunol.1400700. Epub 2014 Jul 25.
3
Probing the biomechanical contribution of the endothelium to lymphocyte migration: diapedesis by the path of least resistance.探究内皮细胞对淋巴细胞迁移的生物力学贡献:通过阻力最小路径的跨内皮迁移。
J Cell Sci. 2014 Sep 1;127(Pt 17):3720-34. doi: 10.1242/jcs.148619. Epub 2014 Jul 7.
4
Isolation of the lateral border recycling compartment using a diaminobenzidine-induced density shift.使用二氨基联苯胺诱导的密度转移分离外侧边界循环区室
Traffic. 2014 Sep;15(9):1016-29. doi: 10.1111/tra.12184. Epub 2014 Jul 1.
5
The RhoA guanine nucleotide exchange factor, LARG, mediates ICAM-1-dependent mechanotransduction in endothelial cells to stimulate transendothelial migration.RhoA 鸟嘌呤核苷酸交换因子 LARG 通过介导内皮细胞中细胞间黏附分子-1 依赖的机械转导来刺激跨内皮迁移。
J Immunol. 2014 Apr 1;192(7):3390-8. doi: 10.4049/jimmunol.1302525. Epub 2014 Feb 28.
6
Leukocyte extravasation and vascular permeability are each controlled in vivo by different tyrosine residues of VE-cadherin.白细胞渗出和血管通透性在体内分别受 VE-钙黏蛋白不同的酪氨酸残基控制。
Nat Immunol. 2014 Mar;15(3):223-30. doi: 10.1038/ni.2824. Epub 2014 Feb 9.
7
Neutrophil and monocyte recruitment by PECAM, CD99, and other molecules via the LBRC.PECAM、CD99和其他分子通过LBRC招募中性粒细胞和单核细胞。
Semin Immunopathol. 2014 Mar;36(2):193-209. doi: 10.1007/s00281-013-0412-6. Epub 2013 Dec 12.
8
How T cells trigger the dissociation of the endothelial receptor phosphatase VE-PTP from VE-cadherin.T 细胞如何触发内皮受体磷酸酶 VE-PTP 与 VE-钙黏蛋白的解离。
Blood. 2013 Oct 3;122(14):2512-22. doi: 10.1182/blood-2013-04-499228. Epub 2013 Aug 1.
9
Release of cellular tension signals self-restorative ventral lamellipodia to heal barrier micro-wounds.细胞张力信号的释放使自我修复的腹侧片状伪足能够修复屏障微创伤。
J Cell Biol. 2013 Apr 29;201(3):449-65. doi: 10.1083/jcb.201209077.
10
Neutrophil transmigration: emergence of an adhesive cascade within venular walls.中性粒细胞迁移:血管壁内黏附级联反应的出现。
J Innate Immun. 2013;5(4):336-47. doi: 10.1159/000346659. Epub 2013 Mar 2.

跨内皮迁移的调控:新知识与新问题

The regulation of transendothelial migration: new knowledge and new questions.

作者信息

Muller William A

机构信息

Department of Pathology, Northwestern University Feinberg School of Medicine, Ward Building 3-140, 303 East Chicago Avenue, Chicago, IL 60611, USA

出版信息

Cardiovasc Res. 2015 Aug 1;107(3):310-20. doi: 10.1093/cvr/cvv145. Epub 2015 May 17.

DOI:10.1093/cvr/cvv145
PMID:25987544
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4592322/
Abstract

Leucocyte transendothelial migration (TEM) involves a co-operative series of interactions between surface molecules on the leucocyte and cognate counter-ligands on the endothelial cell. These interactions set up a cascade of signalling events inside the endothelial cell that both allow for the junctions to loosen and for membrane to be recruited from the lateral border recycling compartment (LBRC). The LBRC is thought to provide an increased surface area and unligated receptors to the leucocyte to continue the process. The relative importance of the individual adhesion/signalling molecules that promote transmigration may vary depending on the type of leucocyte, the vascular bed, the inflammatory stimulus, and the stage of the inflammatory response. However, the molecular interactions between leucocyte and endothelial cell activate signalling pathways that disengage the adherens and tight junctions and recruit the LBRC to the site of transmigration. With the exception of disengaging the junctions, similar molecules and mechanisms promote transcellular migration as paracellular migration of leucocytes. This review will discuss the molecular interactions and signalling pathways that regulate transmigration, and the common themes that emerge from studying TEM of different leucocyte subsets under different inflammatory conditions. We will also raise some unanswered questions in need of future research.

摘要

白细胞跨内皮迁移(TEM)涉及白细胞表面分子与内皮细胞上同源反配体之间一系列协同相互作用。这些相互作用在内皮细胞内引发一系列信号事件,既使连接变得松弛,又能从侧向边界回收区(LBRC)募集膜。LBRC被认为可为白细胞提供增加的表面积和未结合的受体,以继续这一过程。促进迁移的各个黏附/信号分子的相对重要性可能因白细胞类型、血管床、炎症刺激以及炎症反应阶段而异。然而,白细胞与内皮细胞之间的分子相互作用激活信号通路,使黏附连接和紧密连接分离,并将LBRC募集到迁移部位。除了使连接分离外,相似的分子和机制促进白细胞的跨细胞迁移和平行细胞迁移。本综述将讨论调节迁移的分子相互作用和信号通路,以及在不同炎症条件下研究不同白细胞亚群的TEM所呈现出的共同主题。我们还将提出一些有待未来研究解答的问题。