首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Protective Effect of Resveratrol against IL-1β-Induced Inflammatory Response on Human Osteoarthritic Chondrocytes Partly via the TLR4/MyD88/NF-κB Signaling Pathway: An in Vitro Study
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Protective Effect of Resveratrol against IL-1β-Induced Inflammatory Response on Human Osteoarthritic Chondrocytes Partly via the TLR4/MyD88/NF-κB Signaling Pathway: An in Vitro Study

机译:白藜芦醇对IL-1β诱导的人骨关节炎软骨细胞炎症反应的保护作用部分通过TLR4 / MyD88 /NF-κB信号传导途径进行:体外研究

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摘要

Resveratrol is a natural polyphenolic compound that prevents inflammation in chondrocytes and animal models of osteoarthritis (OA) via yet to be defined mechanisms. The purpose of this study was to determine whether the protective effect of resveratrol on IL-1β-induced human articular chondrocytes was associated with the TLR4/MyD88/NF-κB signaling pathway by incubating human articular chondrocytes (harvested from osteoarthritis patients) with IL-1β before treatment with resveratrol. Cell viability was evaluated using the MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay and TNFα levels in culture supernatants were measured by ELISA(Enzymelinked immunosorbent assay). The levels of TLR4 and its downstream signaling targets (MyD88 and TRAF6) and IL-1β were assessed by measuring the levels of mRNA and protein expression by real-time RT-PCR and western blot analysis, respectively, in addition to assessing NF-κB activation. In addition, TLR4 siRNA was used to block TLR4 expression in chondrocytes further demonstrating that resveratrol prevented IL-1β-mediated inflammation by TLR4 inhibition. We found that resveratrol prevented IL-1β-induced reduction in cell viability. Stimulation of chondrocytes with IL-1β caused a significant up-regulation of TLR4 and its downstream targets MyD88 and TRAF6 resulting in NF-κB activation associated with the synthesis of IL-1β and TNFα. These IL-1β-induced inflammatory responses were all effectively reversed by resveratrol. Furthermore, activation of NF-κB in chondrocytes treated with TLR4 siRNA was significantly attenuated, but not abolished, and exposure to resveratrol further reduced NF-κB translocation. These data suggested that resveratrol prevented IL-1β-induced inflammation in human articular chondrocytes at least in part by inhibiting the TLR4/MyD88/NF-κB signaling pathway suggesting that resveratrol has the potential to be used as a nutritional supplement to counteract OA symptoms.
机译:白藜芦醇是一种天然多酚化合物,可通过尚待确定的机制防止软骨细胞和骨关节炎(OA)动物模型的炎症。这项研究的目的是确定白藜芦醇对IL-1β诱导的人软骨细胞的保护作用是否与TLR4 / MyD88 /NF-κB信号通路相关联,方法是将人关节软骨细胞(从骨关节炎患者身上采集)与IL-白藜芦醇治疗前为1β。使用MTT(3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑鎓溴化物)测定法评估细胞生存力,并通过ELISA(酶联免疫吸附测定法)测量培养上清液中的TNFα水平。除了评估NF-κB外,还通过实时RT-PCR和蛋白质印迹分析分别测量mRNA和蛋白质表达水平,从而评估TLR4及其下游信号传导靶标(MyD88和TRAF6)和IL-1β的水平激活。此外,TLR4 siRNA用于阻断软骨细胞中TLR4的表达,进一步证明白藜芦醇通过抑制TLR4阻止了IL-1β介导的炎症。我们发现白藜芦醇可以阻止IL-1β诱导的细胞活力降低。用IL-1β刺激软骨细胞会导致TLR4及其下游靶点MyD88和TRAF6明显上调,从而导致与IL-1β和TNFα合成相关的NF-κB活化。白藜芦醇可有效逆转这些IL-1β诱导的炎症反应。此外,用TLR4 siRNA处理的软骨细胞中NF-κB的激活显着减弱,但没有消除,暴露于白藜芦醇可进一步减少NF-κB的移位。这些数据表明白藜芦醇至少部分地通过抑制TLR4 / MyD88 /NF-κB信号传导通路来预防IL-1β诱导的人关节软骨细胞炎症,这表明白藜芦醇具有用作抵抗OA症状的营养补充剂的潜力。

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