Aghajanian A, Wittchen E S, Allingham M J, Garrett T A, Burridge K
Department of Cell and Developmental Biology and Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
J Thromb Haemost. 2008 Sep;6(9):1453-60. doi: 10.1111/j.1538-7836.2008.03087.x. Epub 2008 Jul 19.
The endothelial lining of the vasculature forms the physical barrier between the blood and underlying tissues. Junctions between adjacent endothelial cells are dynamically modulated to sustain vascular homeostasis and to support the transendothelial migration of leukocytes during inflammation. A variety of factors initiate intracellular signaling pathways that regulate the opening and resealing of junctional complexes. This review focuses on three primary signaling pathways initiated within endothelial cells by the binding of vasoactive factors and leukocyte adhesion: Rho GTPases, reactive oxygen species, and tyrosine phosphorylation of junctional proteins. These pathways converge to regulate junctional permeability, either by affecting the stability of junctional proteins or by modulating their interactions. Although much progress has been made in understanding the relationships of these pathways, many questions remain to be answered. A full understanding of the signaling cascades that affect endothelial junctions should identify novel therapeutic targets for diseases that involve excessive permeability or inappropriate leukocyte infiltration into tissues.
血管的内皮衬里形成了血液与下方组织之间的物理屏障。相邻内皮细胞之间的连接会动态调节,以维持血管稳态,并在炎症期间支持白细胞的跨内皮迁移。多种因素启动细胞内信号通路,调节连接复合体的开放和重新封闭。本综述重点关注由血管活性因子结合和白细胞黏附在内皮细胞内引发的三种主要信号通路:Rho GTP酶、活性氧以及连接蛋白的酪氨酸磷酸化。这些通路通过影响连接蛋白的稳定性或调节其相互作用来共同调节连接通透性。尽管在理解这些通路的关系方面已经取得了很大进展,但仍有许多问题有待解答。全面了解影响内皮连接的信号级联反应,应能为涉及通透性过高或白细胞不适当浸润组织的疾病确定新的治疗靶点。