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Article
Nature Structural Biology  10, 995 - 1001 (2003)
Published online: 9 November 2003; | doi:10.1038/nsb1011

Bistable regulation of integrin adhesiveness by a bipolar metal ion cluster

JianFeng Chen, Azucena Salas & Timothy A Springer

The CBR Institute of Biomedical Research and Department of Pathology, Harvard Medical School, Boston, Massachusetts 02115, USA.

Correspondence should be addressed to Timothy A Springer springeroffice@cbr.med.harvard.edu
Integrin alpha4beta7 mediates rolling adhesion in Ca2+ and Ca2+ + Mg2+, and firm adhesion in Mg2+ and Mn2+, mimicking the two key steps in leukocyte accumulation in inflamed vasculature. We mutated an interlinked linear array of three divalent cation-binding sites present in integrin beta-subunit I-like domains. The middle, metal ion−dependent adhesion site (MIDAS) is required for both rolling and firm adhesion. One polar site, that adjacent to MIDAS (ADMIDAS), is required for rolling because its mutation results in firm adhesion. The other polar site, the ligand-induced metal binding site (LIMBS), is required for firm adhesion because its mutation results in rolling. The LIMBS mediates the positive regulatory effects of low Ca2+ concentrations, whereas the ADMIDAS mediates the negative regulatory effects of higher Ca2+ concentrations, which are competed by Mn2+. The bipolar sites thus stabilize two alternative phases of adhesion.

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REFERENCE
Immunological Adhesion and Homing Molecules
Nature Encyclopaedia of Life Sciences
 See all 6 matches for Reference

REVIEWS
Therapeutic antagonists and conformational regulation of integrin function
Nature Reviews Drug Discovery Review (01 Sep 2003)
 See all 4 matches for Reviews

NEWS AND VIEWS
From crystal clear ligand binding to designer I domains
Nature Structural Biology News and Views (01 Aug 2000)

RESEARCH
Chemokine Induction of Integrin Adhesiveness on Rolling and Arrested Leukocytes Local Signaling Events or Global Stepwise Activation?
Microcirculation Original Article (20 Jun 2003)
Arrest Chemokines
Microcirculation Original Article (20 Jun 2003)
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Nature Structural & Molecular Biology
ISSN: 1545-9993
EISSN: 1545-9985
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