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FNDC5 通过 AMPK 介导的巨噬细胞极化减轻肥胖中的脂肪组织炎症和胰岛素抵抗。

FNDC5 attenuates adipose tissue inflammation and insulin resistance via AMPK-mediated macrophage polarization in obesity.

机构信息

Key Laboratory of Targeted Intervention of Cardiovascular Disease, Collaborative Innovation Center of Translational Medicine for Cardiovascular Disease, and Department of Physiology, Nanjing Medical University, Nanjing, Jiangsu 211166, China.

Department of Cardiac Surgery, The Second Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu 211166, China.

出版信息

Metabolism. 2018 Jun;83:31-41. doi: 10.1016/j.metabol.2018.01.013. Epub 2018 Jan 31.

Abstract

BACKGROUND

Obesity-induced chronic inflammation is critical in the pathogenesis of insulin resistance, and the recruitment and proinflammatory activation of adipose tissue macrophages (ATMs) is important for the development of this process. Here, we examined the effects of fibronectin type III domain-containing 5 (FNDC5) on inflammation and insulin resistance in high-fat diet-induced obese mice.

MATERIALS AND METHODS

Male wild-type (WT) and FNDC5 mice were fed with standard chow (Ctrl) or high fat diet (HFD) for 20 weeks to induce obesity and insulin resistance. Firstly, effects of FNDC5 gene deletion on obesity, insulin resistance, macrophage accumulation and polarization and adipose tissue inflammation were determined in mice. Secondly, the macrophage polarity shift was further examined with flow cytometry in isolated stromal vascular fraction (SVF). Thirdly, the effects of exogenous FNDC5 on lipopolysaccharide (LPS)-induced macrophage polarization, inflammation and the underlying signaling mechanism were investigated in RAW264.7 macrophages and primary mouse peritoneal cavity macrophages (PMs). Finally, the therapeutic effects of FNDC5 overexpression were examined in HFD-induced obese WT and FNDC5 mice.

RESULTS

FNDC5 gene deletion aggravated obesity, insulin resistance, fat accumulation and inflammation accompanied with enhanced AMPK inhibition, macrophages recruitment and M1 polarization in mice fed with HFD. Exogenous FNDC5 inhibited LPS-induced M1 macrophage polarization and inflammatory cytokine production via AMPK phosphorylation in both RAW264.7 macrophages and PMs. FNDC5 overexpression attenuated insulin resistance, AMPK inhibition, M1 macrophage polarization and inflammatory cytokine production in adipose tissue of obese WT and FNDC5 mice.

CONCLUSIONS

FNDC5 attenuates adipose tissue inflammation and insulin resistance via AMPK-mediated macrophage polarization in HFD-induced obesity. FNDC5 plays several beneficial roles in obesity and may be used as a therapeutic regimen for preventing inflammation and insulin resistance in obesity and diabetes.

摘要

背景

肥胖引起的慢性炎症在胰岛素抵抗的发病机制中至关重要,脂肪组织巨噬细胞(ATMs)的募集和促炎激活对于这一过程的发展很重要。在这里,我们研究了纤维连接蛋白 III 型结构域 5(FNDC5)对高脂肪饮食诱导肥胖小鼠炎症和胰岛素抵抗的影响。

材料和方法

雄性野生型(WT)和 FNDC5 小鼠分别用标准饲料(Ctrl)或高脂肪饮食(HFD)喂养 20 周,以诱导肥胖和胰岛素抵抗。首先,研究 FNDC5 基因缺失对肥胖、胰岛素抵抗、巨噬细胞积累和极化以及脂肪组织炎症的影响。其次,通过分离基质血管部分(SVF)中的流式细胞术进一步研究巨噬细胞极性变化。然后,研究外源性 FNDC5 对脂多糖(LPS)诱导的巨噬细胞极化、炎症及潜在信号机制的影响。最后,研究 FNDC5 过表达在 HFD 诱导的肥胖 WT 和 FNDC5 小鼠中的治疗效果。

结果

FNDC5 基因缺失加剧了 HFD 喂养小鼠的肥胖、胰岛素抵抗、脂肪堆积和炎症,同时增强了 AMPK 抑制、巨噬细胞募集和 M1 极化。外源性 FNDC5 通过 LPS 诱导的 RAW264.7 巨噬细胞和 PMs 中 AMPK 磷酸化抑制 M1 巨噬细胞极化和炎症细胞因子的产生。FNDC5 过表达减轻了肥胖 WT 和 FNDC5 小鼠脂肪组织中的胰岛素抵抗、AMPK 抑制、M1 巨噬细胞极化和炎症细胞因子的产生。

结论

FNDC5 通过 AMPK 介导的巨噬细胞极化减轻 HFD 诱导肥胖中的脂肪组织炎症和胰岛素抵抗。FNDC5 在肥胖中发挥了多种有益作用,可作为预防肥胖和糖尿病中炎症和胰岛素抵抗的治疗方案。

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