枫叶黄酮抑制脂多糖诱导破骨前体细胞Raw264.7细胞激活的作用
Flavonoid Isolated from the Leaves of Acer Truncatum Bunge Inhibits Lipopolysaccharide-induced Activation of Raw264.7 Cells
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摘要: [摘要]目的 探讨枫叶黄酮对脂多糖 (lipopolysaccharide,LPS)诱导破骨前体细胞Raw264.7细胞炎性因子释放的抑制作用.方法 用LPS (5 mg/mL)刺激Raw264.7细胞构建炎症模型,采用四甲基偶氮唑蓝比色法 (MTT)检测Raw264.7细胞的活力影响;酶联免疫吸附试验(ELISA)检测一氧化氮 (NO)和前列腺素E2 , PGE2表达;运用免疫荧光染色方法检测诱导型一氧化氮合酶和环氧合酶-2,COX-2、子肿瘤坏死因子-αTNF-α和白介素-1β,IL-1β、核因子-κB,NF-κB蛋白与mRNA的表达变化. 结果 不同浓度的枫叶黄酮明显抑制了LPS诱导的Row246.7细胞NO、PGE2,iNOS和COX-2,TNF-α和IL-1β与NF-κB的上调,并且NO、PGE2、iNOS、COX-2和NF-κB蛋白的表达呈剂量依赖性. 结论 枫叶黄酮可抑制LPS诱导的破骨前体细胞Raw264.7细胞iNOS、COX-2和NF-κB/P65蛋白表达和炎性因子释放从而抑制破骨细胞的激活
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关键词:
- [关键词]枫叶黄酮 /
- 脂多糖 /
- 炎性因子 /
- Raw264.7细胞 /
- 免疫荧光染色
Abstract: [Abstract]Objective To investigate the inhibitory effects of flavonoid isolated from the leaves of Acer truncatum Bunge on the expression of pro-inflammatory cytokines in Raw264.7 cells stimulated with lipopolysaccharide (LPS).Methods Inflammatory cell model was structured by LPS-stimulated Raw264.7 cells,the cells were treated with flavonoid(10 μM, 30 μM and 60 μM) prior to LPS(5 mg/mL)exposure and the effects of flavonoid on viability of Raw264.7 cells were measured by MTT assay,Nitric oxide(NO)and prostaglandin E2 (PGE2)were measured by ELISA,the effects on the protein levels of pro-inflammatory enzymes,cyclooxygenase-2(COX-2)and inducible nitric oxide synthase(iNOS),and pro-inflammatory cytokines,tumor necrosis factor-α(TNF-α),and interleukin-1β(IL-1β),inflammatory signaling proteins nuclear factor-κB (NF-κB)were analysed by immunofl uorescence staining assay.Results LPS-induced NO,PGE2,iNOS, COX-2 and NF-κB protein expression levels were significantly decreased by flavonoid in a concentration-dependent manner and flavonoid also had an effect on the expression of TNF-α,IL-1β through translational inhibition. Conclusion Flavonoid isolated from the leaves of Acer truncatum Bunge can inhibit LPS-induced activation of Raw264.7 cells through inhibiting the release of pro-infl ammatory mediators,then exerts its anti-osteoporosis activities.
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