S100A9 mediates neutrophil adhesion to fibronectin through activation of β2 integrins

被引：67

作者：

Anceriz, Nadia ^{[1
]}

Vandal, Karen ^{[1
]}

Tessier, Philippe A. ^{[1
]}

机构：

[1] Univ Laval, Ctr Hosp, Infext Dis Res Ctr, Quebec City, PQ G1V 4G2, Canada

来源：

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS | 2007年 / 354卷 / 01期

关键词：

S100; proteins; adhesion molecules; extracellular matrix; inflammation; integrins;

D O I：

10.1016/j.bbrc.2006.12.203

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：

Neutrophil migration from the blood to inflammatory sites follows a cascade of events, in which adhesion to endothelial cells and extracellular matrix proteins is essential. S100A8, S100A9, and S100A12 are small abundant proteins found in human neutrophil cytosol and presumed to be involved in leukocyte migration. Here we investigated the 5100 proteins' activities in neutrophil tissue migration by evaluating their effects on neutrophil adhesion to certain extracellular matrix proteins. S100A9 induced adhesion only to fibronectin and was the only 5100 protein that stimulated neutrophil adhesion to this extracellular matrix protein. Experiments with blocking antibodies revealed that neither beta 1 nor beta 3 integrins were strongly involved in neutrophil adhesion to fibronectin, contrary to what the literature predicted. In contrast, neutrophil adhesion to fibronectin was completely inhibited by anti-beta 2 integrins, suggesting that S100A9-induced specific activation of beta 2 integrin is essential to neutrophil adhesion. (c) 2006 Elsevier Inc. All rights reserved.

引用

页码：84 / 89

页数：6