首页> 美国卫生研究院文献>Biochemistry and Biophysics Reports >Tetracyclines downregulate the production of LPS-induced cytokines and chemokines in THP-1 cells via ERK p38 and nuclear factor-κB signaling pathways
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Tetracyclines downregulate the production of LPS-induced cytokines and chemokines in THP-1 cells via ERK p38 and nuclear factor-κB signaling pathways

机译:四环素通过ERKp38和核因子-κB信号通路下调THP-1细胞中LPS诱导的细胞因子和趋化因子的产生

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摘要

Recent reports have shown that antibiotics such as macrolide, aminoglycoside, and tetracyclines have immunomodulatory effects in addition to essential antibiotic effects. These agents may have important effects on the regulation of cytokine and chemokine production. However, the precise mechanism is unknown. This time, we used Multi Plex to measure the production of cytokines and chemokines following tetracycline treatment of lipopolysaccharide (LPS)-induced THP-1 cells. The signaling pathways were investigated with Western blotting analysis. Three tetracyclines significantly suppressed the expression of cytokines and chemokines induced by LPS. Minocycline (50 μg/ml), tigecycline (50 μg/ml), or doxycycline (50 μg/ml) were added after treatment with LPS (10 μg/ml). Tumor necrosis factor-α was downregulated to 16%, 14%, and 8%, respectively, after 60 min compared to treatment with LPS without agents. Interleukin-8 was downregulated to 43%, 32%, and 26% at 60 min. Macrophage inflammatory protein (MIP)-1α was downregulated to 23%, 33%, and 16% at 120 min. MIP-1β was downregulated to 21%, 11%, and 2% at 120 min. Concerning about signaling pathways, the mechanisms of the three tetracyclines might not be the same. Although the three tetracyclines showed some differences in the time course, tetracyclines modulated phosphorylation of the NF-κB pathway, p38 and ERK1/2/MAPK pathways, resulting in inhibition of cytokine and chemokine production. In addition, SB203580 (p38 inhibitor) and U0126 (ERK1/2 inhibitor) significantly suppressed the expression of TNF-α and IL-8 in LPS-stimulated THP-1 cells. And further, the NF-κB inhibitor, BAY11-7082, almost completely suppressed LPS-induced these two cytokines production. Thus, more than one signaling pathway may be involved in tetracyclines downregulation of the expression of LPS-induced cytokines and chemokines in THP-1 cells. And among the three signaling pathways, NF-κB pathway might be the dominant pathway on tetracyclines modification the LPS-induced cytokines production in THP-1 cells. In general, minocycline and doxycycline suppressed the production of cytokines and chemokines in LPS-stimulated THP-1 cell lines via mainly the inhibition of phosphorylation of NF-κB pathways. Tigecycline has the same structure as the other tetracyclines, however, it showed the different properties of cytokine modulation in the experimental time course.
机译:最近的报道表明,除必需的抗生素作用外,大环内酯,氨基糖苷和四环素等抗生素还具有免疫调节作用。这些试剂可能对细胞因子和趋化因子产生的调节具有重要作用。但是,确切的机制尚不清楚。这次,我们使用Multi Plex来测量四环素处理脂多糖(LPS)诱导的THP-1细胞后细胞因子和趋化因子的产生。用蛋白质印迹分析研究信号传导途径。三个四环素显着抑制LPS诱导的细胞因子和趋化因子的表达。用LPS(10μg/ ml)处理后,添加了米诺环素(50μg/ ml),替加环素(50μg/ ml)或强力霉素(50μg/ ml)。与未使用LPS的LPS治疗相比,在60分钟后,肿瘤坏死因子-α分别下调至16%,14%和8%。在60分钟时,白介素8被下调至43%,32%和26%。 120分钟时巨噬细胞炎症蛋白(MIP)-1α被下调至23%,33%和16%。 MIP-1β在120分钟时下调至21%,11%和2%。关于信号传导途径,三种四环素的机制可能不相同。尽管三个四环素在时间上显示出一些差异,但四环素可调节NF-κB途径,p38和ERK1 / 2 / MAPK途径的磷酸化,从而抑制细胞因子和趋化因子的产生。此外,SB203580(p38抑制剂)和U0126(ERK1 / 2抑制剂)可显着抑制LPS刺激的THP-1细胞中TNF-α和IL-8的表达。此外,NF-κB抑制剂BAY11-7082几乎完全抑制LPS诱导的这两种细胞因子的产生。因此,四环素下调THP-1细胞中LPS诱导的细胞因子和趋化因子的表达可能涉及一个以上的信号通路。在这三种信号通路中,NF-κB通路可能是四环素修饰LPS诱导的THP-1细胞中细胞因子产生的主要途径。通常,米诺环素和强力霉素主要通过抑制NF-κB途径的磷酸化来抑制LPS刺激的THP-1细胞系中细胞因子和趋化因子的产生。替加环素与其他四环素具有相同的结构,但是在实验过程中它显示出不同的细胞因子调节特性。

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