α4β7 integrin mediates lymphocyte binding to the mucosal vascular addressin MAdCAM-1

Cornelia Berlin, Ellen L. Berg, Michael J. Briskin, David P. Andrew, Peter J. Kilshaw, Bernhard Holzmann, Irving L. Weissman, Alf Hamann, Eugene C. Butcher

Research output: Contribution to journalArticlepeer-review

1360 Scopus citations

Abstract

The mucosal vascular addressin, MAdCAM-1, is an immunoglobulin superfamily adhesion molecule for lymphocytes that is expressed by mucosal venules and helps direct lymphocyte traffic into Peyer's patches (PP) and the intestinal lamina propria. We demonstrate that the lymphocyte integrin α4β7, also implicated in homing to PP, is a receptor for MAdCAM-1. Certain antibodies to α4 and β7 integrin chains but not to the β2 integrin LFA-1 inhibit lymphocyte binding to purified MAdCAM-1 and to MAdCAM-1 transfectants. Lymph node lymphocytes, α4β7+ TK1 lymphoma cells, and a β7-transfected variant of an α4+ B cell line, 38C13, bind constitutively to MAdCAM-1. Binding is enhanced by Mn++-induced integrin activation. The related integrin α4β1 supports efficient binding to VCAM-1 but not to MAdCAM-1, even after integrin activation, indicating that MAdCAM-1 is a preferential ligand for α4β7. α4β7 can also bind VCAM-1, but this requires greater integrin activation than binding to MAdCAM-1. The findings imply a selective role for the interaction of α4β7 and MAdCAM-1 lymphocyte in homing to mucosal sites.

Original languageEnglish
Pages (from-to)185-195
Number of pages11
JournalCell
Volume74
Issue number1
DOIs
StatePublished - 16 Jul 1993
Externally publishedYes

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