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糙皮侧耳与松口蘑共培养发酵液总黄酮通过 MAPK 信号通路对 LPS 刺激的 RAW264.7 巨噬细胞发挥抗炎作用。

Total flavones of fermentation broth by co-culture of Coprinus comatus and Morchella esculenta induces an anti-inflammatory effect on LPS-stimulated RAW264.7 macrophages cells via the MAPK signaling pathway.

机构信息

College of Life Science and Technology, Dalian University, Liaoning, 116622, China.

Department of Engineering Physics, Institute of Medical Physics, Tsinghua University, Beijing, 100084, China.

出版信息

Microb Pathog. 2018 Dec;125:431-437. doi: 10.1016/j.micpath.2018.10.008. Epub 2018 Oct 10.

DOI:10.1016/j.micpath.2018.10.008
PMID:30316005
Abstract

The inflammatory cellular model of RAW264.7 cells induced by lipopolysaccharide (LPS) has always been used to investigate the effect of anti-inflammatory agents in vitro. In the present study, the anti-inflammatory activity of total flavones extracted from the fermentation broth of the co-culture of Coprinus comatus and Morchella esculenta (MCF-F), and its potential molecular mechanism in LPS-challenged RAW264.7 macrophage cells were investigated. The data revealed that MCF-F exhibited anti-inflammatory activity in LPS-stimulated RAW264.7 cells. At the same time, MCF-F was less cytotoxic under a concentration of 16 μg/ml in RAW264.7 cells. The anti-inflammatory activity of MCF-F was detected using the Griess method and ELISA assay, and the results well-corroborated with the observed decrease in expression in pro-inflammatory mediators, including nitric oxide, tumor necrosis factor-α and inteleukin-1β (IL-1β). In addition, the expression of inducible NO synthase (iNOS) and cyclooxygenase2 (COX-2) were confirmed by RT-PCR and western blot, and it was found that both mRNA and protein levels were downregulated after MCF-F treatment. The data also revealed that MCF-F downregulated the phosphorylation of JNK, ERK and P38 MAPK. Collectively, these results lead to the conclusion that MCF-F exerts an anti-inflammatory effect against LPS-challenged RAW264.7 cells via the MAPK pathway.

摘要

脂多糖(LPS)诱导的 RAW264.7 细胞炎症细胞模型一直被用于体外研究抗炎剂的作用。本研究探讨了毛栓菌和皱盖假芝共培养发酵液总黄酮(MCF-F)对 LPS 刺激的 RAW264.7 巨噬细胞的抗炎活性及其潜在的分子机制。数据表明 MCF-F 对 LPS 刺激的 RAW264.7 细胞具有抗炎活性。同时,在 16μg/ml 的浓度下,MCF-F 在 RAW264.7 细胞中的细胞毒性较小。通过格里斯法和 ELISA 测定法检测 MCF-F 的抗炎活性,结果与观察到的促炎介质表达下降(包括一氧化氮、肿瘤坏死因子-α和白细胞介素-1β)非常吻合。此外,通过 RT-PCR 和 Western blot 证实诱导型一氧化氮合酶(iNOS)和环氧化酶 2(COX-2)的表达,发现 MCF-F 处理后 mRNA 和蛋白水平均下调。数据还表明 MCF-F 下调了 JNK、ERK 和 P38 MAPK 的磷酸化。综上所述,这些结果表明 MCF-F 通过 MAPK 通路对 LPS 刺激的 RAW264.7 细胞发挥抗炎作用。

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