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Fisetin Inhibits Lipopolysaccharide-Induced Macrophage Activation and Dendritic Cell Maturation

机译:Fisetin抑制脂多糖诱导的巨噬细胞激活和树突状细胞成熟。

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摘要

Macrophages and dendritic cells are required for initiating innate immunity and adaptive immunity. Aberrant activation of macrophages and dendritic cells can cause detrimental immune responses; thus, agents effectively modulating their functions are of great clinical value. We herein investigated whether fisetin, a flavonoid prevalently present in fruits and vegetables, could inhibit macrophage activation and dendritic cell maturation. Fisetin suppressed LPS-induced NF-κB activation, expression of pro-inflammatory proteins (TNF-α and iNOS), MMP-9 activity, and phagocytic activity in macrophages. Furthermore, upon LPS-induced dendritic cell maturation, fisetin at nontoxic concentrations suppressed the expression of costimulatory molecules (CD80 and CD86), the production of cytokines (IL-12, IL-6, and TNF-α), and the endocytic activity of dendritic cells. Fisetin treatment significantly attenuated migration of dendritic cells into spleens and dendritic cell-mediated T cell activation in LPS-treated mice. Collectively, our data reveal that fisetin inhibits macrophage activation and impairs functional maturation of dendritic cells.
机译:巨噬细胞和树突状细胞是启动先天免疫和适应性免疫所必需的。巨噬细胞和树突状细胞的异常激活会引起有害的免疫反应。因此,有效调节其功能的药物具有很大的临床价值。我们在本文中研究了非瑟酮(一种普遍存在于水果和蔬菜中的类黄酮)是否可以抑制巨噬细胞的活化和树突状细胞的成熟。 Fisetin抑制巨噬细胞中LPS诱导的NF-κB活化,促炎蛋白(TNF-α和iNOS)的表达,MMP-9活性和吞噬活性。此外,在LPS诱导的树突状细胞成熟后,非毒性浓度的非瑟定抑制了共刺激分子(CD80和CD86)的表达,细胞因子(IL-12,IL-6和TNF-α)的产生以及内吞活性。树突状细胞。 Fisetin处理可显着减弱LPS处理的小鼠中树突状细胞向脾脏的迁移以及树突状细胞介导的T细胞活化。总的来说,我们的数据表明,非瑟酮抑制巨噬细胞的活化并损害树突状细胞的功能成熟。

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