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调节 L-选择素依赖性白细胞黏附和迁移的信号。

Signals regulating L-selectin-dependent leucocyte adhesion and transmigration.

机构信息

Membrane/Cytoskeleton Signalling Group, Cardiovascular Division, British Heart Foundation, Centre of Research Excellence, King's College London, London SE5 9NU, United Kingdom.

出版信息

Int J Biochem Cell Biol. 2013 Mar;45(3):550-5. doi: 10.1016/j.biocel.2012.12.023. Epub 2013 Jan 5.

DOI:10.1016/j.biocel.2012.12.023
PMID:23299028
Abstract

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. naïve 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.

摘要

L-选择素是一种 I 型跨膜细胞黏附分子,存在于大多数循环白细胞的表面。L-选择素敲除小鼠的研究表明,这种糖蛋白在健康和疾病中起着重要作用,调节白细胞向周围淋巴结(如幼稚 T 细胞)和急性及慢性炎症部位(如单核细胞和中性粒细胞)的募集。临床试验表明,L-选择素是某些急性和慢性炎症性疾病有前途的治疗靶点。揭示 L-选择素下游的细胞内信号也可能以细胞类型/疾病特异性的方式揭示新的治疗靶点。这篇综述将重点介绍 L-选择素依赖的信号转导——探讨多步骤黏附级联反应的不同阶段可能产生的不同信号,以及 L-选择素已知结合伙伴在这一反应中的作用。

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