Department of Cell Biology, UCL Institute of Ophthalmology, University College London, London, UK.
Neuropathol Appl Neurobiol. 2011 Feb;37(1):24-39. doi: 10.1111/j.1365-2990.2010.01140.x.
Leucocyte migration into the central nervous system is a key stage in the development of multiple sclerosis. While much has been learnt regarding the sequential steps of leucocyte capture, adhesion and migration across the vasculature, the molecular basis of leucocyte extravasation is only just being unravelled. It is now recognized that bidirectional crosstalk between the immune cell and endothelium is an essential element in mediating diapedesis during both normal immune surveillance and under inflammatory conditions. The induction of various signalling networks, through engagement of cell surface molecules such as integrins on the leucocyte and immunoglobulin superfamily cell adhesion molecules on the endothelial cell, play a major role in determining the pattern and route of leucocyte emigration. In this review we discuss the extent of our knowledge regarding leucocyte migration across the blood-brain barrier and in particular the endothelial cell signalling pathways contributing to this process.
白细胞迁移到中枢神经系统是多发性硬化症发展的关键阶段。虽然已经了解了白细胞捕获、黏附和穿过血管迁移的连续步骤,但白细胞渗出的分子基础才刚刚被揭示。现在人们认识到,免疫细胞和内皮细胞之间的双向串扰是在正常免疫监视和炎症条件下介导穿胞作用的重要因素。通过细胞表面分子(如白细胞上的整合素和内皮细胞上的免疫球蛋白超家族细胞黏附分子)的结合,诱导各种信号网络,在决定白细胞迁移的模式和途径方面发挥着重要作用。在这篇综述中,我们讨论了我们对白细胞穿过血脑屏障迁移的了解程度,特别是对内皮细胞信号通路的了解,这些通路有助于这一过程。