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崖爬藤属植物根中的黄酮类化合物通过抑制TLR4/MD-2介导的JNK和NF-κB信号通路发挥抗炎作用。

Flavonoids from Radix Tetrastigmae inhibit TLR4/MD-2 mediated JNK and NF-κB pathway with anti-inflammatory properties.

作者信息

Liu Dandan, Cao Gang, Han Likai, Ye Yilu, SiMa Yuhan, Ge Weihong

机构信息

Pharmaceutical College, Zhejiang Chinese Medical University, 546 Binwen Road, Hangzhou 310053, China; Department of Basic medicine, Hangzhou Medical College, 481 Binwen Road, Hangzhou 310053, China.

Pharmaceutical College, Zhejiang Chinese Medical University, 546 Binwen Road, Hangzhou 310053, China.

出版信息

Cytokine. 2016 Aug;84:29-36. doi: 10.1016/j.cyto.2015.08.003. Epub 2016 May 25.

Abstract

Radix Tetrastigmae (RT) has immunomodulatory activity, particularly on inflammation and the flavonoids from RT (RTFs) are one of the main components. In this study, we detected the anti-inflammation potential of RTFs in LPS-induced RAW264.7 cells and tried to uncover the underlying mechanism. Results demonstrated that RTFs (10-160μg/ml) treatment significantly decreased LPS-induced production of pro-inflammatory mediators, including NO, IL-1β, TNF-α, IL-6, IL-12p40, sTNF-R1 and increased anti-inflammatory cytokine IL-10 expression in macrophages in a dose-dependent manner. Molecular research showed the up-regulated expression of TLR4, MD-2, MyD88 and TLR4/MD-2 complex induced by LPS were attenuated after RTFs treatment. Furthermore, phosphorylation and activity of JNK and NF-κB, two important downstream signaling molecules of TLR4/MD-2 pathway, were also changed along with TLR4/MD-2 complex. But no significant phosphorylation was observed on p38 and ERK. In conclusion, RTFs contribute to the regulation of LPS-induced inflammatory response in RAW264.7 cells through TLR4/MD-2 mediated NF-κB and JNK pathway. It may be a potential choice for the treatment of inflammation diseases.

摘要

四棱豆根(RT)具有免疫调节活性,尤其是对炎症的调节作用,且RT中的黄酮类化合物(RTFs)是主要成分之一。在本研究中,我们检测了RTFs在脂多糖(LPS)诱导的RAW264.7细胞中的抗炎潜力,并试图揭示其潜在机制。结果表明,RTFs(10 - 160μg/ml)处理可显著降低LPS诱导的促炎介质的产生,包括一氧化氮(NO)、白细胞介素-1β(IL-1β)、肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)、白细胞介素-12p40、可溶性肿瘤坏死因子受体1(sTNF-R1),并以剂量依赖的方式增加巨噬细胞中抗炎细胞因子白细胞介素-10(IL-10)的表达。分子研究表明,RTFs处理后,LPS诱导的Toll样受体4(TLR4)、髓样分化蛋白2(MD-2)、髓样分化因子88(MyD88)和TLR4/MD-2复合物的表达上调受到抑制。此外,TLR4/MD-2途径的两个重要下游信号分子JNK和核因子κB(NF-κB)的磷酸化和活性也随TLR4/MD-2复合物的变化而改变。但未观察到p38和细胞外信号调节激酶(ERK)有明显的磷酸化。总之,RTFs通过TLR4/MD-2介导的NF-κB和JNK途径参与调节LPS诱导的RAW264.7细胞炎症反应。它可能是治疗炎症性疾病的一个潜在选择。

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