Constantinescu C S, Grygar C, Kappos L, Leppert D
Departments of Neurology and Research, University Hospital, Basle, Switzerland.
Cytokine. 2001 Feb 21;13(4):244-7. doi: 10.1006/cyto.2000.0818.
In peripheral blood mononuclear cells (PBMC), matrix metalloproteinase (MMP)-9 mediates the extravasation of immune cells and may be involved in tissue destruction during inflammation. We investigated the effect of the pro-inflammatory cytokines interleukin (IL-)12 and 15 on the secretion of MMP-9 in PBMC. IL-15, but not IL-12, induces MMP-9 in PBMC and in T cells. Moreover, the combination of IL-15 and IL-2 had an additive effect. In contrast, both IL-12 and IL-15 induced the release of tissue inhibitor of metalloproteinases (TIMP)-1. IL-15 led to a dose-dependent increase of the MMP-9/TIMP-1 ratio as a measure for increased proteolytic capacity. We conclude that IL-15 mediates its effects in inflammation in part through MMP-9.
在外周血单核细胞(PBMC)中,基质金属蛋白酶(MMP)-9介导免疫细胞的外渗,并可能参与炎症过程中的组织破坏。我们研究了促炎细胞因子白细胞介素(IL)-12和15对PBMC中MMP-9分泌的影响。IL-15而非IL-12可诱导PBMC和T细胞中的MMP-9。此外,IL-15和IL-2的组合具有相加作用。相比之下,IL-12和IL-15均可诱导金属蛋白酶组织抑制剂(TIMP)-1的释放。作为蛋白水解能力增强的指标,IL-15导致MMP-9/TIMP-1比值呈剂量依赖性增加。我们得出结论,IL-15部分通过MMP-9介导其在炎症中的作用。