邵葵阳, 张璇, 焦文君, 张斯琳, 张学武. 珍珠梅黄酮纳米粒抑制脂多糖诱发肝癌细胞的炎性作用J. 药学学报, 2017,52(10): 1549-1553. doi: 10.16438/j.0513-4870.2017-0432
引用本文: 邵葵阳, 张璇, 焦文君, 张斯琳, 张学武. 珍珠梅黄酮纳米粒抑制脂多糖诱发肝癌细胞的炎性作用J. 药学学报, 2017,52(10): 1549-1553. doi: 10.16438/j.0513-4870.2017-0432
SHAO Kui-yang, ZHANG Xuan, JIAO Wen-jun, ZHANG Si-lin, ZHANG Xue-wu. Anti-inflammatory effect of TTF1-NP on lipopoiysaccharide stimulated human hepatocellular carcinoma cellsJ. Acta Pharmaceutica Sinica, 2017,52(10): 1549-1553. doi: 10.16438/j.0513-4870.2017-0432
Citation: SHAO Kui-yang, ZHANG Xuan, JIAO Wen-jun, ZHANG Si-lin, ZHANG Xue-wu. Anti-inflammatory effect of TTF1-NP on lipopoiysaccharide stimulated human hepatocellular carcinoma cellsJ. Acta Pharmaceutica Sinica, 2017,52(10): 1549-1553. doi: 10.16438/j.0513-4870.2017-0432

珍珠梅黄酮纳米粒抑制脂多糖诱发肝癌细胞的炎性作用

Anti-inflammatory effect of TTF1-NP on lipopoiysaccharide stimulated human hepatocellular carcinoma cells

  • 摘要: 探讨珍珠梅黄酮纳米粒(5,2',4'-trihydroxy-6,7,5'-trimethoxy flavone nanoparticle,TTF1-NP)抑制脂多糖(lipopoiysaccharide,LPS)诱发人肝癌HepG2细胞的炎性作用及调控机制。采用LPS诱发人肝癌HepG2细胞的炎症模型;MTT比色法检测TTF1-NP对人肝癌HepG2细胞增殖作用;Western blot法检测TTF1-NP对LPS诱发的HepG2细胞炎性反应的TLR4和IL-6及AKT/mTOR信号通路关键蛋白的表达作用。结果显示,TTF1-NP能够抑制LPS引起的人肝癌HepG2细胞增殖,抑制TLR4蛋白表达及AKT和mTOR蛋白的磷酸化,抑制炎症因子IL-6和IL-8表达;TTF1-NP抑制胰岛素引起的AKT/mTOR信号通路的活化和TLR4蛋白的表达,从而降低IL-6和IL-8蛋白水平。研究表明,TTF1-NP抑制LPS诱导的人肝癌HepG2细胞的炎性反应,其作用机制可能与AKT/mTOR信号通路有关。

     

    Abstract: The study was designed to test the role of 5,2',4'-trihydroxy-6,7,5'-trimethoxy flavone nanoparticle (TTF1-NP) on lipopoiysaccharide (LPS)-induced inflammatory response, and to explore the anti-inflammatory mechanism in human hepatocellular carcinoma cells. Inflammatory responses were induced in human hepato-cellular carcinoma HepG2 cells with LPS; Proliferation effect of TTF1-NP in LPS-stimulated HepG2 cells were detected by MTT assay; The expression of TLR4, AKT/mTOR signaling related proteins and IL-6 were detected by Western blot assay. The results showed that TTF1-NP inhibited the proliferation of HepG2 cells induced by LPS in a dose-dependent manner; TTF1-NP inhibited the expression of TLR4, the activation of AKT and mTOR, and expression of IL-6 in a dose-dependent manner; TTF1-NP inhibited the activation of AKT/mTOR signaling pathway and TLR4 proteins leading to suppression of IL-6 expression in HepG2 cells stimulated by insulin. These results suggest that TTF1-NP inhibited inflammatory responses from LPS treatment with a potential mechanisms in the inhibition of AKT/mTOR pathway.

     

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