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Interleukin-4 inhibition of interleukin-1-induced expression of matrix metalloproteinase-3 (MMP-3) is independent of lipoxygenase and PPARγ activation in human gingival fibroblasts

机译:白细胞介素4抑制白细胞介素1诱导的基质金属蛋白酶3(MMP-3)表达与人牙龈成纤维细胞中的脂氧合酶和PPARγ活化无关

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摘要

BackgroundInterleukin 4 (IL-4) has been shown to suppress interleukin-1 (IL-1) induced expression of matrix metalloproteinase-3 (MMP-3) in human synovial and gingival fibroblasts, but the mechanism of suppression has not been determined. Activators of peroxisome proliferator-activated receptor-γ (PPARγ) have been shown to inhibit cytokine induced expression of MMPs in other cell types, and IL-4 has been shown to activate PPARγ by stimulating production of ligands through the lipoxygenase pathway. It has been suggested that PPARγ may inhibit expression of MMPs by competing with transcription factor AP-1 for binding to a putative composite binding element in the promoters. The objective of this study was to determine whether the suppressive effects of IL-4 on the IL-1 induced expression of MMP-3 involve activation of lipoxygenase and/or PPARγ.
机译:背景已显示白介素4(IL-4)抑制白细胞介素1(IL-1)诱导的人滑膜和牙龈成纤维细胞中基质金属蛋白酶-3(MMP-3)的表达,但尚未确定其抑制机制。过氧化物酶体增殖物激活受体-γ(PPARγ)的激活物已显示抑制细胞因子诱导的MMP在其他细胞类型中的表达,IL-4已显示通过刺激脂氧合酶途径的配体产生而激活PPARγ。已经提出PPARγ可通过与转录因子AP-1竞争结合启动子中假定的复合结合元件来抑制MMP的表达。这项研究的目的是确定IL-4对IL-1诱导的MMP-3表达的抑制作用是否涉及脂氧合酶和/或PPARγ的激活。

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