Lymphocyte migration into the central nervous system: Implication of ICAM-1 signalling at them blood-brain barrier

被引:103
作者
Greenwood, J
Etienne-Manneville, S
Adamson, P
Couraud, PO
机构
[1] CNRS, UPR 415, Inst Cochin Genet Mol, F-75014 Paris, France
[2] UCL, Inst Ophthalmol, London EC1V 9EL, England
关键词
D O I
10.1016/S1537-1891(02)00199-4
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Lymphocyte recruitment to the central nervous system (CNS) is a critical step in the pathogenesis of diseases such as multiple sclerosis (MS), meningitis and posterior uveitis. The principle sequential stages that control lymphocyte emigration from the blood have been widely reported, but only recently has attention been directed towards the role of the vascular endothelium in actively supporting transvascular migration. It has now been shown that adhesion molecules, particularly those of the immunoglobulin super family (eg ICAM-1, VCAM-1 and PECAM-1), not only act as ligands for leucocyte receptors but can also serve as signal transducers. Engagement of these receptors initiates endothelial signalling cascades that result in downstream effector mechanisms which in turn influence the progression of neuroinflammation. In particular, it has been shown that ICAM-1-mediated signalling in brain endothelial cells is a crucial regulatory step in the process of lymphocyte migration through the blood-brain barrier and as such represents an additional phase in the multistep paradigm of leucocyte recruitment. In this article we review current understanding of endothelial cell ICAM-I signalling and discuss the importance of these findings in relation to leucocyte trafficking to the CNS. (C) 2002 Elsevier Science Inc. All rights reserved.
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收藏
页码:315 / 322
页数:8
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