辛烷酰化Ghrelin抑制THP-1巨噬细胞中棕榈酸诱导的TLR4/NF-κB信号通路的激活

ISRN endocrinology Pub Date : 2012-01-01 Epub Date: 2012-11-26 DOI:10.5402/2012/237613
S P Liu, X Y Li, Z Li, L N He, Y Xiao, K Yan, Z G Zhou
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引用次数: 18

摘要

为了研究酰化ghrelin对棕榈酸诱导的人单核细胞源性(THP-1)巨噬细胞TLR4/NF-κB信号通路激活的影响,采用不同浓度的棕榈酸培养THP-1巨噬细胞12 h。用不同剂量的酰化胃饥饿素预处理THP-1巨噬细胞4 h,再用棕榈酸(200 μmol/L)培养12 h。观察THP-1巨噬细胞中TLR4、NF-κB p65磷酸化水平及培养上清中TNF-α、IL-1β水平。实时荧光定量PCR检测TLR4 mRNA表达。western blotting检测TLR4蛋白表达和NF-κB p65磷酸化水平。ELISA法检测TNF-α、IL-1β的表达。与未加棕榈酸处理的THP-1巨噬细胞相比,棕榈酸处理后TLR4 mRNA蛋白水平、NF-κB p65磷酸化水平及TNF-α、IL-1β表达呈剂量依赖性升高(P < 0.05)。与棕榈酸(200 μmol/L)处理的THP-1巨噬细胞相比,乙酰化胃饥饿素预处理后THP-1巨噬细胞的通透性物质水平呈剂量依赖性降低。因此,我们得出结论,酰化ghrelin可以调节TLR4/NF-κB信号通路的激活,抑制棕榈酸刺激的THP-1巨噬细胞炎症因子的释放,并呈剂量依赖性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Octanoylated Ghrelin Inhibits the Activation of the Palmitic Acid-Induced TLR4/NF-κB Signaling Pathway in THP-1 Macrophages.

To investigate the effect of acylated ghrelin on the activation of TLR4/NF-κB signaling pathway induced by palmitic acid in human monocyte-derived (THP-1) macrophages, THP-1 macrophages were cultured for 12 h by palmitic acid with various concentrations. The THP-1 macrophages was pretreated by acylated ghrelin at different doses for 4 h before cultivated by palmitic acid (200 μmol/L) for 12 h. We observed the level of TLR4, NF-κB p65 phosphorylation in THP-1 macrophages and TNF-α, IL-1β in culture supernatant. TLR4 mRNA was measured by real-time PCR. TLR4 protein and NF-κB p65 phosphorylation was measured by western blotting. The expression of TNF-α and IL-1β was detected by ELISA. Compared to the THP-1 macrophages without palmitic acid, the level of TLR4 mRNA protein and NF-κB p65 phosphorylation and the expression of TNF-α and IL-1β increased after treatment by palmitic acid in a dose-dependent fashion (P < 0.05). Compared to the THP-1 macrophages with palmitic acid (200 μmol/L), the level of the pervious substances decreased after preadministration by acylated ghrelin in a dose-dependent fashion. So, we make a conclusion that acylated ghrelin can regulate the activation of TLR4/NF-κB signaling pathway and inhibit the release of inflammatory cytokines in THP-1 macrophages which are stimulated by palmitic acid in a dose-dependent fashion.

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