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首页> 外文期刊>Frontiers in Pharmacology >4- O-Carboxymethylascochlorin Inhibits Expression Levels of on Inflammation-Related Cytokines and Matrix Metalloproteinase-9 Through NF–κB/MAPK/TLR4 Signaling Pathway in LPS-Activated RAW264.7 Cells
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4- O-Carboxymethylascochlorin Inhibits Expression Levels of on Inflammation-Related Cytokines and Matrix Metalloproteinase-9 Through NF–κB/MAPK/TLR4 Signaling Pathway in LPS-Activated RAW264.7 Cells

机译:4- O -羧甲基氨氯霉素通过NF-κB/ MAPK / TLR4信号通路抑制炎症相关细胞因子和基质金属蛋白酶-9在脂多糖激活的RAW264.7细胞中的表达水平。

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摘要

Toll-like receptor 4 (TLR4) and matrix metalloproteinase-9 (MMP-9) are known to play important roles in inflammatory diseases such as arteriosclerosis and plaque instability. The purpose of this study was to perform the effect of 4- O -carboxymethylascochlorin (AS-6) on MMP-9 expression in lipopolysaccharide (LPS)-induced murine macrophages and signaling pathway involved in its anti-inflammatory effect. Effect of AS-6 on MAPK/NF-κB/TLR4 signaling pathway in LPS-activated murine macrophages was examined using ELISA, Western blotting, reverse transcription polymerase chain reaction (RT-PCR) and fluorescence immunoassay. MMP-9 enzyme activity was examined by gelatin zymography. AS-6 significantly suppressed MMP-9 and MAPK/NF-κB expression levels in LPS-stimulated murine macrophages. Expression levels of inducible nitric oxide synthase (iNOS), COX2, MMP-9, JNK, ERK, p38 phosphorylation, and NF-κB stimulated by LPS were also decreased by AS-6. Moreover, AS-6 suppressed TLR4 expression and dysregulated LPS-induced activators of transcription signaling pathway. The results of this study showed that AS-6 can inhibit LPS-stimulated inflammatory response by suppressing TLR4/MAPK/NF-κB signals, suggesting that AS-6 can be used to induce the stability of atherosclerotic plaque and prevent inflammatory diseases in an in vitro model.
机译:已知Toll样受体4(TLR4)和基质金属蛋白酶9(MMP-9)在炎症性疾病如动脉硬化和斑块不稳定中起重要作用。这项研究的目的是执行4-O-羧甲基阿古霉素(AS-6)对脂多糖(LPS)诱导的鼠巨噬细胞中MMP-9表达的影响以及涉及其抗炎作用的信号通路。使用ELISA,Western印迹,逆转录聚合酶链反应(RT-PCR)和荧光免疫分析法检测了AS-6对LPS激活的鼠巨噬细胞中MAPK /NF-κB/ TLR4信号通路的影响。通过明胶酶谱检查MMP-9酶活性。 AS-6显着抑制LPS刺激的小鼠巨噬细胞中MMP-9和MAPK /NF-κB的表达水平。 LPS刺激的诱导型一氧化氮合酶(iNOS),COX2,MMP-9,JNK,ERK,p38磷酸化和NF-κB的表达水平也被AS-6降低。此外,AS-6抑制TLR4表达,并失调LPS诱导的转录信号通路激活剂。这项研究的结果表明,AS-6可以通过抑制TLR4 / MAPK /NF-κB信号来抑制LPS刺激的炎症反应,这表明AS-6可以用于诱导动脉粥样硬化斑块的稳定性并预防炎症。体外模型。

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