Journal
MUCOSAL IMMUNOLOGY
Volume 4, Issue 1, Pages 66-82Publisher
NATURE PUBLISHING GROUP
DOI: 10.1038/mi.2010.42
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Funding
- NIH [1R01AI074745, 1R56AI080769, 1R01DK076616]
- Crohn's and Colitis Foundation of America
- NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [R56AI080769, R01AI080769, R01AI074745] Funding Source: NIH RePORTER
- NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [R01DK076616] Funding Source: NIH RePORTER
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alpha(4) and beta(7) integrins, such as alpha(4)beta(1), alpha(4)beta(7), and alpha(E)beta(7), are major integrins required for migration of leukocytes into mucosal tissues. The mechanisms responsible for coordinated expression of these three integrins have been poorly elucidated to date. We report that expression of the Itg-alpha(4) subunit by both CD4(+) and CD8(+) T cells requires the retinoic acid signal. In contrast, transcription of Itg-alpha(E) genes is induced by the transforming growth factor-beta 1 (TGF beta 1) signal. Expression of Itg-beta(7) is constitutive but can be further increased by TGF beta 1. Consistently, expression of alpha(4)-containing integrins is severely suppressed in vitamin A deficiency with a compensatory increase of alpha(E)beta(7), whereas expression of Itg-alpha(E) and Itg-beta(7) is decreased in TGF beta-signal deficiency with a compensatory increase in alpha(4)beta(1). The retinoic acid-mediated regulation of alpha(4) integrins is required for specific migration of T cells in vitro and in vivo. These results provide central regulatory mechanisms for coordinated expression of the major mucosal integrins.
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