Triggering of the CD44 antigen on T lymphocytes promotes T cell adhesion through the LFA-1 pathway

The CD44 molecule, a molecule which has been previously known as Hermes, Pgp-1, extracellular matrix receptor III, and In(Lu)-related p80, is currently thought to be involved in several steps of normal immune cell function, including lymphocyte adhesion to high endothelial venules and to the extrace...

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Published inThe Journal of immunology (1950) Vol. 145; no. 11; pp. 3589 - 3592
Main Authors Koopman, G, van Kooyk, Y, de Graaff, M, Meyer, CJ, Figdor, CG, Pals, ST
Format Journal Article
LanguageEnglish
Published Bethesda, MD Am Assoc Immnol 01.12.1990
American Association of Immunologists
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Summary:The CD44 molecule, a molecule which has been previously known as Hermes, Pgp-1, extracellular matrix receptor III, and In(Lu)-related p80, is currently thought to be involved in several steps of normal immune cell function, including lymphocyte adhesion to high endothelial venules and to the extracellular matrix and T cell activation. We now demonstrate that triggering of CD44 on T lymphocytes by anti-CD44 mAb promotes cell adhesion. The induced homotypic adhesion is mediated by lymphocyte function-associated antigen-1 (LFA-1), because it was inhibited by anti-LFA-1 antibodies and not by anti-LFA-3 antibodies. This notion is supported by the temperature and Mg2+ dependence which is characteristic of LFA-1-mediated adhesion. Moreover, the sensitivity of CD44-induced adhesion to AMG and H7, which both prevent the activation of protein kinase C, and to cytochalasin B, which inhibits microfilament formation, suggests that the activation of the LFA-1 pathway via CD44 involves protein kinase C activation and requires an intact cytoskeleton.
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ISSN:0022-1767
1550-6606
DOI:10.4049/jimmunol.145.11.3589