Signals regulating L-selectin-dependent leucocyte adhesion and transmigration

被引:52
作者
Ivetic, Aleksandar [1 ]
机构
[1] Kings Coll London, Ctr Res Excellence, British Heart Fdn, Membrane Cytoskeleton Signalling Grp,Cardiovasc D, London SE5 9NU, England
关键词
Calmodulin; Ezrin-Radixin-Moesin; Inflammation; L-selectin; Leucocyte; CYTOPLASMIC DOMAIN; ERM PROTEINS; IN-VIVO; RECEPTOR; NEUTROPHILS; CALMODULIN; MIGRATION; LYMPHOCYTES; ACTIVATION; ALPHA;
D O I
10.1016/j.biocel.2012.12.023
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
L-selectin is a type I transmembrane cell adhesion molecule that is expressed on the surface of most circulating leukocytes. Studies in L-selectin knockout mice reveal a prominent role for this glycoprotein in health and disease, regulating leucocyte recruitment to peripheral lymph nodes (e.g. naive T-cells) and sites of acute and chronic inflammation (e.g. monocytes and neutrophils). Clinical trials have revealed L-selectin as a promising target in some acute and chronic inflammatory diseases. Unearthing the intracellular signals that act directly downstream of L-selectin may also expose novel therapeutic targets in a cell type/disease-specific manner. This review will focus on L-selectin-dependent signalling - exploring the different signals that potentially arise from distinct phases of the multi-step adhesion cascade and the contribution of known binding partners of L-selectin in this response. (c) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:550 / 555
页数:6
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