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α-萘黄酮通过NFκB信号通路调节脂肪细胞与巨噬细胞相互作用中的炎症反应。

α-Naphthoflavone modulates inflammatory response in adipocytes-macrophages interaction through NFκB signaling.

作者信息

Sun Yanmei, Xie Minghua, Huang Tingting, Zhang Xu, Lei Sicong, Shi Qun, Wang Suqing, Fan Cuifang, Zhang Jie

机构信息

Department of Obstetrics and Gynecology, Renmin Hospital, Wuhan University China.

Department of Nutrition and Food Hygiene, School of Public Health, Wuhan University China.

出版信息

Int J Clin Exp Pathol. 2014 Oct 15;7(11):7768-74. eCollection 2014.

Abstract

OBJECTIVE

Our previous study demonstrated that α-naphthoflavone (α-NF) inhibits mouse 3T3-L1 pre-adipocytes differentiation via PPARγ, a key transcription factor in adipogenesis. Due to the critical role of inflammation in adipogenesis, we speculated that the suppression role of α-NF in adipogenesis might involve in modulation of cytokines secretion raised by adipocyte differentiation cocktail. Therefore, the present study aims to investigate the role of α-NF in modulating of inflammatory response during adipocytes differentiation and adipocyte-macrophage interaction.

METHODS

Conditioned medium from different doses of α-NF treated 10-day differentiated 3T3-L1 adipocytes were collected to culture RAW264.7 macrophages. Conditioned medium from activated macrophages and α-NF pre-treated macrophage were used to investigate the effects of α-NF in adipocytes differentiation. Cultured cells and medium were harvested for RT-PCR, Western blot and ELISA.

RESULTS

α-NF dose-dependently decreased TNF-α and IL-6 and increased IL-10 expression induced by IDM (Insulin, dexamethasone, isobutylmethylxanthine) in 3T3-L1 pre-adipocytes. Conditioned medium from α-NF treated 3T3-L1 differentiated cells inhibited inflammatory response in mouse macrophage cell line RAW264.7 in contrast to IDM control medium. NFĸB activation elicited by IDM was suppressed by α-NF in a dose-response manner. Consequently, decreased TNF-α and increased IL-10 secretion, downstream targets of NFĸB signaling pathway, were observed with α-NF in macrophages. Finally, Conditioned medium from α-NF pre-treated, LPS-activated macrophages ameliorated the suppression of 3T3-L1 adipogenesis by LPS activated macrophages.

CONCLUSION

Our results suggest that α-NF regulates inflammation response in both adipocytes and macrophages and adipocyte-macrophage interaction which contributes to pre-adipocyte differentiation.

摘要

目的

我们之前的研究表明,α-萘黄酮(α-NF)通过过氧化物酶体增殖物激活受体γ(PPARγ)抑制小鼠3T3-L1前脂肪细胞分化,PPARγ是脂肪生成中的关键转录因子。由于炎症在脂肪生成中起关键作用,我们推测α-NF在脂肪生成中的抑制作用可能涉及调节脂肪细胞分化混合物引发的细胞因子分泌。因此,本研究旨在探讨α-NF在调节脂肪细胞分化和脂肪细胞-巨噬细胞相互作用过程中炎症反应的作用。

方法

收集不同剂量α-NF处理10天的分化3T3-L1脂肪细胞的条件培养基,用于培养RAW264.7巨噬细胞。用活化巨噬细胞和α-NF预处理巨噬细胞的条件培养基来研究α-NF对脂肪细胞分化的影响。收集培养的细胞和培养基用于逆转录聚合酶链反应(RT-PCR)、蛋白质免疫印迹法(Western blot)和酶联免疫吸附测定(ELISA)。

结果

α-NF以剂量依赖的方式降低3T3-L1前脂肪细胞中由胰岛素、地塞米松、异丁基甲基黄嘌呤(IDM)诱导的肿瘤坏死因子-α(TNF-α)和白细胞介素-6(IL-6)的表达,并增加白细胞介素-10(IL-10)的表达。与IDM对照培养基相比,α-NF处理的3T3-L1分化细胞的条件培养基抑制了小鼠巨噬细胞系RAW264.7中的炎症反应。α-NF以剂量反应方式抑制IDM引起的核因子κB(NFκB)激活。因此,在巨噬细胞中观察到,作为NFκB信号通路下游靶点的TNF-α分泌减少和IL-10分泌增加。最后,α-NF预处理、脂多糖(LPS)激活的巨噬细胞的条件培养基改善了LPS激活的巨噬细胞对3T3-L1脂肪生成的抑制作用 。

结论

我们的结果表明,α-NF调节脂肪细胞和巨噬细胞中的炎症反应以及脂肪细胞-巨噬细胞相互作用,这有助于前脂肪细胞分化。

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