实验动物与比较医学 ›› 2018, Vol. 38 ›› Issue (6): 434-439.DOI: 10.3969/j.issn.1674-5817.2018.06.006

• 论著 • 上一篇    下一篇

灵芝多糖对脂多糖诱导的巨噬细胞TLR4/NF-κB通路调控及下游炎症因子的影响

杨燕燕, 谢金东, 周建华, 林玮, 王训立   

  1. 福建中医药大学,福州 350122
  • 收稿日期:2018-06-25 出版日期:2018-12-25 发布日期:2021-03-01
  • 作者简介:杨燕燕(1985-),女,助理研究员,硕士研究生。E-mail:yanfjtcm@163.com
  • 基金资助:
    福建省科技计划引导性项目(2015Y0062)

Effects of Ganoderma Lucidum Polysaccharides on TLR4/NF-κB and Downstream Signal Transduction Pathway Activated by Lipopolysaccharide in Macrophage

YANG Yan-yan, XIE Jin-dong, ZHOU Jian-hua, LIN Wei, WANG Xun-Ii   

  1. Fujian University of Traditional Chinese Medicine,Fuzhou 350122,China
  • Received:2018-06-25 Online:2018-12-25 Published:2021-03-01

摘要: 目的 探讨灵芝多糖(GLPs)对脂多糖(LPS)刺激的RAW264.7巨噬细胞Toll样受体4(TLR4)核因子-κB(NF-κB)信号通路及炎症因子的影响机制。方法 体外实验分为5组,分别为对照组,LPS组及GLPs药物低、中、高剂量组。除对照组外,其余均用l µg/mL LPS刺激16 h,药物组分别同时给予GLPs 40 µg/mL、80 µg/mL、160 µg/mL干预2 h,收集细胞。采用实时荧光定量PCR和Western blotting方法测定TLR4、髓样分化因子88(MyD88)、NF-κB、肿瘤坏死因子受体相关因子-6(TRAF-6)、肿瘤坏死因子-α(TNF-α)及植物血凝素样氧化低密度脂蛋白受体-1(LOX-1)的mRNA和蛋白表达情况。结果 与对照组相比,LPS组小鼠RAW264.7细胞TLR4、MyD88、NF-κB及TRAF-6 mRNA表达明显升高(P<0.05)。采用GLPs干预后显著抑制TLR4、MyD88、NF-κB及TRAF-6的表达,与LPS组相比,GLPs中、高剂量组TLR4、MyD88、TRAF-6 mRNA及GLPs低、中、高剂量组NF-κB mRNA均具有显著性差异(P<0.05)。各组的TLR4、MyD88、NF-κB及TRAF-6蛋白表达趋势与mRNA基本一致。与对照组相比,LPS组小鼠RAW264.7细胞TNF-α、LOX-1 mRNA水平显著升高(P<0.01),采用GLPs干预后TNF-α、LOX-1 mRNA均显著低于LPS组(P<0.05)。各组的TNF-α、LOX-1蛋白表达趋势与mRNA基本一致。结论 GLPs可阻断TLR4高表达及下游MyD88依赖性途径,还可明显抑制TNF-α、LOX-1等炎症因子的表达。

关键词: 灵芝多糖(GLPs), 巨噬细胞, Toll样受体4(TLR4), 核因子-κB(NF-κB), 炎性细胞因子

Abstract: Objective To investigate the inhibitory effects of ganoderma lucidum polysaccharides (GLPs) on toll like receptor 4 (TLR4) signal transduction pathways and inflammatory cytokines regulating mechanism activateby lipopolysaccharide (LPS) in macrophage. Method Macrophage was stimulated with LPS for 16 hours and treated with the GLPs (low dose group 40 µg/mL, mid dose group 80 µg/mL, high dose group 160 µg/mL) for 2 hours simultaneously. In basis of this, the real-time fluorescent quantitative PCR and Western blotting methods were used to respectively detecting mRNA and protein of all groups of TLR4, myeloid differentiation factor 88 (MyD88), nuclear factor-kappa B (NF-κB), tumor necrosis factor receptor-associated factor 6 (TRAF-6), tumor necrosis factor alpha (TNF-α) and lectin-like oxidized low-density lipoprotein receptor-1 (LOX-1). Result (1) The mRNA relative expression were activated of TLR4 and primary element of downstream MyD88 dependent signal transduction pathway in LPS group, such as TLR4, MyD88, NF-κB and TRAF-6, which had significant differences compared with normal group (P<0.05). The GLPs could restrain in a degree the mRNA expression of TLR4, MyD88, NF-κB and TRAF-6 after being interfered in. The TLR4, MyD88 and TRAF-6 mRNA of GLPs-Mid and GLPs-High dose group had significant differences compared with LPS group (P<0.05). The NF-κB mRNA of all GLPs groups had significant differences compared with LPS group (P<0.05). And then, the relative expression of TLR4, MyD88, NF-κB and TRAF-6 protein in each group was consistent with the expression of mRNA. (2) Compared with normal group, the mRNA expression of TNF-α and LOX-1 were significantly increased in LPS group (P<0.05). The GLPs could restrain in a degree the mRNA expression of TNF-α and LOX-1 after being interfered in, which had significant differences compared with LPS group (P<0.05). And then, the expression of TNF-α and LOX-1 protein in each group was consistent with the expression of mRNA. Conclusion It was speculated that GLPs might restrain the expression of TLR4 and primary element of downstream MyD88 dependent signal transduction pathway. It was also illustrated that GLPs might restrain the expression of inflammatory cytokines such as TNF-α and LOX-1.

Key words: Ganoderma lucidum polysaccharides (GLPs), Macrophage, Toll like receptor 4 (TLR4), Nuclear factor-kappa B (NF-кB), Inflammatory cytokines

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