Liver-specific p70 S6 Kinase Depletion Protects against Hepatic Steatosis and Systemic Insulin Resistance

被引:56
作者
Bae, Eun Ju
Xu, Jianfeng
Oh, Da Young
Bandyopadhyay, Gautam
Lagakos, William S.
Keshwani, Malik [2 ]
Olefsky, Jerrold M. [1 ]
机构
[1] Univ Calif San Diego, Dept Med, Div Endocrinol & Metab, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Pharmacol, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
DIET-INDUCED OBESITY; MAMMALIAN TARGET; AMINO-ACIDS; RAPAMYCIN PATHWAY; RAT HEPATOCYTES; LIPOGENESIS; ACTIVATION; MICE; AKT; SENSITIVITY;
D O I
10.1074/jbc.M112.365544
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:18769 / 18780
页数:12
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