Muller William A
Department of Pathology, Northwestern University Feinberg School of Medicine, Ward Building 3-140, 303 East Chicago Avenue, Chicago, IL 60611, USA
Cardiovasc Res. 2015 Aug 1;107(3):310-20. doi: 10.1093/cvr/cvv145. Epub 2015 May 17.
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.
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。