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微小RNA-199a-3p通过靶向Sp1减弱肝脏脂肪生成。

MicroRNA-199a-3p attenuates hepatic lipogenesis by targeting Sp1.

作者信息

Cheng Yang, Huang Li, Ping Jian, Chen Tianyang, Chen Jianjie

机构信息

Hospital for Infectious Diseases of Pudong New AreaShanghai 201299, P. R. China.

Institute of Liver Disease, Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese MedicineShanghai 201203, P. R. China.

出版信息

Am J Transl Res. 2017 Apr 15;9(4):1905-1913. eCollection 2017.

Abstract

Emerging studies have demonstrated that microRNAs (miRs) are profoundly involved in non-alcoholic fatty liver disease (NAFLD) and related metabolic diseases. Previously, we revealed a repertoire of miRs dysregulated in NAFLD by high-throughput sequencing. Here, we showed that microRNA-199a-3p was down-regulated in the livers of C57BL/6J mice fed a high-fat-diet (HFD) and oleic acid/palmitic acid-induced Hepa1-6 cells. Gain-of-function and loss-of-function studies demonstrated that microRNA-199a-3p exhibited a suppressive role in hepatic lipogenesis. Adenoviral mediated microRNA-199a-3p expression in C57BL/6J mice largely attenuated triglyceride (TG) accumulation and expression of lipogenic genes. Furthermore, we identified Specificity Protein 1 (Sp1) as the functional target of miR-124. Restoration of Sp1 expression largely compromised the effect of microRNA-199a-3p on hepatic TG metabolism. Taken together, our findings uncover a novel function of microRNA-199a-3p/Sp1 axis in NAFLD and provide a mechanism underlying perturbations of hepatic TG homeostasis.

摘要

新兴研究表明,微小RNA(miRs)与非酒精性脂肪性肝病(NAFLD)及相关代谢性疾病密切相关。此前,我们通过高通量测序揭示了NAFLD中失调的一组miRs。在此,我们发现高脂饮食(HFD)喂养的C57BL/6J小鼠肝脏及油酸/棕榈酸诱导的Hepa1-6细胞中,微小RNA-199a-3p表达下调。功能获得和功能缺失研究表明,微小RNA-199a-3p在肝脏脂肪生成中起抑制作用。腺病毒介导的微小RNA-199a-3p在C57BL/6J小鼠中的表达显著减弱了甘油三酯(TG)积累和脂肪生成基因的表达。此外,我们确定特异性蛋白1(Sp1)是miR-124的功能靶点。Sp1表达的恢复在很大程度上削弱了微小RNA-199a-3p对肝脏TG代谢的影响。综上所述,我们的研究结果揭示了微小RNA-199a-3p/Sp1轴在NAFLD中的新功能,并提供了肝脏TG稳态失衡的潜在机制。

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