The extracellular matrix protein mindin serves as an integrin ligand and is critical for inflammatory cell recruitment.

Abstract:

:Leukocyte recruitment to inflammation sites depends on interactions between integrins and extracellular matrix (ECM). In this report we show that mice lacking the ECM protein mindin exhibit severely impaired recruitment of neutrophils and macrophages in 4 different inflammation models. Furthermore, neutrophils directly bind to immobilized mindin, and mindin matrix mediates neutrophil migration in vitro. The adhesion of neutrophils to mindin is blocked by anti-integrin alpha4, anti-integrin alpha(M), and anti-integrin beta2 antibodies. We also show that HEK-293 cells transfected with cDNA encoding these integrins exhibit enhanced binding to immobilized mindin matrix and the increased binding can be blocked by anti-integrin antibodies. Our results suggest that mindin serves as a novel ligand for integrins and mindin-integrin interactions are critical for inflammatory cell recruitment in vivo.

journal_name

Blood

journal_title

Blood

authors

Jia W,Li H,He YW

doi

10.1182/blood-2005-04-1658

subject

Has Abstract

pub_date

2005-12-01 00:00:00

pages

3854-9

issue

12

eissn

0006-4971

issn

1528-0020

pii

2005-04-1658

journal_volume

106

pub_type

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