4.7 Article

The alternatively spliced αEC domain of human fibrinogen-420 is a novel ligand for leukocyte integrins αMβ2 and αXβ2

期刊

BLOOD
卷 98, 期 8, 页码 2448-2455

出版社

AMER SOC HEMATOLOGY
DOI: 10.1182/blood.V98.8.2448

关键词

-

资金

  1. NHLBI NIH HHS [HL-51050, HL-63199] Funding Source: Medline

向作者/读者索取更多资源

The interaction of human plasma fibrinogen with leukocyte integrins alpha (M)beta (2) (CD11b/ CD18, Mac-1) and alpha (X)beta (2) (CD11c/CD18, p150,95) is an important component of the inflammatory response. Previously, it was demonstrated that binding of fibrinogen to these integrins is mediated by gammaC, the globular C-terminal domain of the gamma chain. In this study, evidence was found of another fibrinogen domain that can serve as a ligand for the 2 leukocyte integrins: alpha C-E, a homologous domain that extends the a chains in a recently discovered subclass of fibrinogen known as fibrinogen-420. Recombinant alpha C-E supported strong adhesion and migration of cells expressing alpha (M)beta (2) and alpha (x)beta (2), including nonactivated and activated U937 and THP-1 monocytoid cells, and neutrophils. Cells transfected with complementary DNA for these integrins also bound alpha C-E. The specificity of interaction was substantiated by inhibition of cell adhesion with antibodies against alpha (M), alpha (x), and beta (2) subunits. Also, neutrophil inhibitory factor, a specific inhibitor of alpha (M)beta (2) and alpha (x)beta (2) function, efficiently blocked cell adhesion to alpha C-E. In alpha (M)beta (2) and alpha (x)beta (2), the I domain is the binding site for alpha C-E, since alpha C-E bound to recombinant alpha (M) I and alpha I-x domains in a dose-dependent and saturable manner. Synthetic peptides that duplicated sequences gamma 190 to 202 and gamma 377 to 395, previously considered putative binding sites in gammaC, effectively inhibited alpha (M)beta (2)- and alpha (x)beta (2)-mediated adhesion to alpha C-E, suggesting that recognition of alpha C-E by the I domain involves structural features in common with those of gammaC. These findings identify alpha C-E as a second domain in fibrinogen-420 that binds alpha (M)beta (2) and alpha (x)beta (2) and can mediate leukocyte adhesion and migration. (C) 2001 by The American Society of Hematology.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据