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本文引用的文献

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mTOR complex 1 regulates lipin 1 localization to control the SREBP pathway.mTOR 复合物 1 调节脂滴包被蛋白 1 的定位以控制 SREBP 通路。
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Akt stimulates hepatic SREBP1c and lipogenesis through parallel mTORC1-dependent and independent pathways.Akt 通过平行的 mTORC1 依赖性和非依赖性途径刺激肝 SREBP1c 和脂肪生成。
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GPR120 is an omega-3 fatty acid receptor mediating potent anti-inflammatory and insulin-sensitizing effects.GPR120 是一种 omega-3 脂肪酸受体,具有强大的抗炎和胰岛素增敏作用。
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Bifurcation of insulin signaling pathway in rat liver: mTORC1 required for stimulation of lipogenesis, but not inhibition of gluconeogenesis.胰岛素信号通路在大鼠肝脏中的分支:mTORC1 促进脂肪生成,而不是抑制糖异生。
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Akt2 is required for hepatic lipid accumulation in models of insulin resistance.Akt2 是胰岛素抵抗模型中肝脂质积累所必需的。
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SIRT1 exerts anti-inflammatory effects and improves insulin sensitivity in adipocytes.沉默调节蛋白1(SIRT1)发挥抗炎作用并改善脂肪细胞中的胰岛素敏感性。
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SREBP activity is regulated by mTORC1 and contributes to Akt-dependent cell growth.固醇调节元件结合蛋白(SREBP)的活性受哺乳动物雷帕霉素靶蛋白复合物1(mTORC1)调控,并促进Akt依赖的细胞生长。
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肝特异性 p70 S6 激酶缺失可预防肝脂肪变性和全身胰岛素抵抗。

Liver-specific p70 S6 kinase depletion protects against hepatic steatosis and systemic insulin resistance.

机构信息

Department of Medicine, University of California, San Diego, California 92093, USA.

出版信息

J Biol Chem. 2012 May 25;287(22):18769-80. doi: 10.1074/jbc.M112.365544. Epub 2012 Apr 9.

DOI:10.1074/jbc.M112.365544
PMID:22493495
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3365775/
Abstract

Obesity-associated hepatic steatosis is a manifestation of selective insulin resistance whereby lipogenesis remains sensitive to insulin but the ability of insulin to suppress glucose production is impaired. We created a mouse model of liver-specific knockdown of p70 S6 kinase (S6K) (L-S6K-KD) by systemic delivery of an adeno-associated virus carrying a shRNA for S6K and examined the effects on steatosis and insulin resistance. High fat diet (HFD) fed L-S6K-KD mice showed improved glucose tolerance and systemic insulin sensitivity compared with controls, with no changes in food intake or body weight. The induction of lipogenic gene expression was attenuated in the L-S6K-KD mice with decreased sterol regulatory element-binding protein (SREBP)-1c expression and mature SREBP-1c protein, as well as decreased steatosis on HFD. Our results demonstrate the importance of S6K: 1) as a modulator of the hepatic response to fasting/refeeding, 2) in the development of steatosis, and 3) as a key node in selective hepatic insulin resistance in obese mice.

摘要

肥胖相关性肝脂肪变性是胰岛素抵抗的一种表现形式,其特征是脂肪生成仍然对胰岛素敏感,但胰岛素抑制葡萄糖生成的能力受损。我们通过系统递送携带 S6K 短发夹 RNA 的腺相关病毒,创建了一种肝脏特异性敲低 p70 S6 激酶 (S6K) 的小鼠模型 (L-S6K-KD),并研究了其对肝脂肪变性和胰岛素抵抗的影响。与对照组相比,高脂肪饮食 (HFD) 喂养的 L-S6K-KD 小鼠表现出改善的葡萄糖耐量和全身胰岛素敏感性,而食物摄入量或体重没有变化。L-S6K-KD 小鼠的脂肪生成基因表达诱导减弱,固醇调节元件结合蛋白 (SREBP)-1c 表达和成熟 SREBP-1c 蛋白减少,HFD 上的脂肪变性减少。我们的结果表明 S6K 的重要性:1) 作为对禁食/再喂养的肝脏反应的调节剂,2) 在脂肪变性的发展中,以及 3) 在肥胖小鼠的选择性肝胰岛素抵抗中的关键节点。