Kohka H, Yoshino T, Iwagaki H, Sakuma I, Tanimoto T, Matsuo Y, Kurimoto M, Orita K, Akagi T, Tanaka N
First Department of Surgery, Okayama University School of Medicine, Shikata, Japan.
J Leukoc Biol. 1998 Oct;64(4):519-27. doi: 10.1002/jlb.64.4.519.
Intercellular adhesion molecule-1 (ICAM-1, CD54) is a membrane glycoprotein and a member of the immunoglobulin superfamily. It plays a central role in cell to cell-mediated immune responses and is a ligand for leukocyte function-associated antigen-1 (LFA-1). We report here that a newly discovered cytokine, interferon-gamma-inducing factor (IGIF) [H. Okamura et al. (1995) Nature 378, 88] recently proposed to be designated as IL-18, selectively up-regulates ICAM-1 expression in KG-1 cells, a human myelomonocytic cell line, in which IL-18 also enhances interferon-gamma production. IL-18 induced heterotypic aggregation between KG-1 and Peer T cells, which was blocked by anti-ICAM-1 and/or LFA-1 antibodies. Anti-interferon-gamma antibody did not block the IL-18-induced up-regulation of ICAM-1 on KG-1 cells. These results thus show that IGIF/IL-18, enhances ICAM-1 expression in KG-1 cells in an interferon-gamma-independent pathway, up-regulates ICAM-1 functions, and that IL-18 might play a potential role in immunoregulation by mediating immune cell infiltration into the tissues.
细胞间黏附分子-1(ICAM-1,CD54)是一种膜糖蛋白,属于免疫球蛋白超家族成员。它在细胞间介导的免疫反应中起核心作用,是白细胞功能相关抗原-1(LFA-1)的配体。我们在此报告,一种新发现的细胞因子,即干扰素-γ诱导因子(IGIF)[H. Okamura等人(1995年)《自然》378, 88],最近提议将其命名为IL-18,可选择性地上调人骨髓单核细胞系KG-1细胞中ICAM-1的表达,在该细胞系中IL-18还可增强干扰素-γ的产生。IL-18诱导KG-1细胞与Peer T细胞之间的异型聚集,这可被抗ICAM-1和/或LFA-1抗体阻断。抗干扰素-γ抗体不能阻断IL-18诱导的KG-1细胞上ICAM-1的上调。因此,这些结果表明,IGIF/IL-18以一种不依赖干扰素-γ的途径增强KG-1细胞中ICAM-1的表达,上调ICAM-1的功能,并且IL-18可能通过介导免疫细胞向组织内浸润在免疫调节中发挥潜在作用。