Koopman G, van Kooyk Y, de Graaff M, Meyer C J, Figdor C G, Pals S T
Department of Pathology, Free University, Amsterdam, The Netherlands.
J Immunol. 1990 Dec 1;145(11):3589-93.
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.
CD44分子,一种先前被称为Hermes、Pgp-1、细胞外基质受体III和In(Lu)相关p80的分子,目前被认为参与正常免疫细胞功能的多个步骤,包括淋巴细胞与高内皮微静脉和细胞外基质的黏附以及T细胞活化。我们现在证明,抗CD44单克隆抗体触发T淋巴细胞上的CD44可促进细胞黏附。诱导的同型黏附由淋巴细胞功能相关抗原-1(LFA-1)介导,因为它被抗LFA-1抗体抑制而不被抗LFA-3抗体抑制。这一观点得到了LFA-1介导黏附所特有的温度和Mg2+依赖性的支持。此外,CD44诱导的黏附对均能阻止蛋白激酶C活化的AMG和H7以及抑制微丝形成的细胞松弛素B的敏感性表明,通过CD44激活LFA-1途径涉及蛋白激酶C活化且需要完整的细胞骨架。