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Blood, 1 December 2005, Vol. 106, No. 12, pp. 3854-3859. Prepublished online as a Blood First Edition Paper on August 16, 2005; DOI 10.1182/blood-2005-04-1658.
IMMUNOBIOLOGY The extracellular matrix protein mindin serves as an integrin ligand and is critical for inflammatory cell recruitmentFrom the Department of Immunology, Duke University Medical Center, Durham, NC.
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
This article has been cited by other articles:
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| Copyright © 2005 by American Society of Hematology Online ISSN: 1528-0020 | |||||||||
4, anti–integrin 
2 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. 
