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阴阳 1 通过抑制肥胖小鼠法尼醇 X 受体促进肝脂肪变性。

Yin Yang 1 promotes hepatic steatosis through repression of farnesoid X receptor in obese mice.

机构信息

Department of Endocrine and Metabolic Diseases, Shanghai Institute of Endocrinology and Metabolism, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, , Shanghai, China.

出版信息

Gut. 2014 Jan;63(1):170-8. doi: 10.1136/gutjnl-2012-303150. Epub 2013 Jan 24.

Abstract

BACKGROUND

Non-alcoholic fatty liver disease (NAFLD) is characterised by accumulation of excessive triglycerides in the liver. Obesity is usually associated with NAFLD through an unknown mechanism.

OBJECTIVE

To investigate the roles of Yin Yang 1 (YY1) in the progression of obesity-associated hepatosteatosis.

METHODS

Expression levels of hepatic YY1 were identified by microarray analysis in high-fat-diet (HFD)-induced obese mice. Liver triglyceride metabolism was analysed in mice with YY1 overexpression and suppression.

RESULTS

YY1 expression was markedly upregulated in HFD-induced obese mice and NAFLD patients. Overexpression of YY1 in healthy mice promoted hepatosteatosis under high-fat dietary conditions, whereas liver-specific ablation of YY1 using adenoviral shRNA ameliorated triglyceride accumulation in obese mice. At the molecular level, YY1 suppressed farnesoid X receptor (FXR) expression through binding to the YY1 responsive element at intron 1 of the FXR gene.

CONCLUSIONS

These findings indicate that YY1 plays a crucial role in obesity-associated hepatosteatosis, through repression of FXR expression.

摘要

背景

非酒精性脂肪性肝病(NAFLD)的特征是肝脏中积聚过多的甘油三酯。肥胖通常通过未知机制与 NAFLD 相关。

目的

研究 Yin Yang 1(YY1)在肥胖相关脂肪性肝病进展中的作用。

方法

通过微阵列分析鉴定高脂肪饮食(HFD)诱导肥胖小鼠中肝脏 YY1 的表达水平。在 YY1 过表达和抑制的小鼠中分析肝内甘油三酯代谢。

结果

YY1 在 HFD 诱导的肥胖小鼠和非酒精性脂肪性肝病患者中表达明显上调。在高脂肪饮食条件下,健康小鼠中 YY1 的过表达促进了脂肪性肝病,而使用腺病毒 shRNA 特异性敲除 YY1 可改善肥胖小鼠的甘油三酯蓄积。在分子水平上,YY1 通过与 FXR 基因内含子 1 上的 YY1 反应元件结合来抑制法尼醇 X 受体(FXR)的表达。

结论

这些发现表明,YY1 通过抑制 FXR 的表达在肥胖相关脂肪性肝病中起关键作用。

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