miR-23a/b-3p promotes hepatic lipid accumulation by regulating Srebp-1c and Fas.

IF 3.6 4区 医学 Q2 ENDOCRINOLOGY & METABOLISM
Linfang Li, Xiaoyi Zhang, Hangjiang Ren, Xiuqing Huang, Tao Shen, Weiqing Tang, Lin Dou, Jian Li
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引用次数: 11

Abstract

miR-23a-3p and miR-23b-3p are members of the miR-23~27~24-2 superfamily. The role of miR-23a/b-3p in regulating hepatic lipid accumulation is still unknown. Here, we found that increased miR-23a-3p and miR-23b-3p levels were accompanied by an increase in the protein levels of the sterol regulatory element-binding protein-1 (SREBP-1) and fatty acid synthase (FAS) in the steatotic livers of mice fed a high-fat diet and leptin receptor-deficient type 2 diabetic mice (db/db). Importantly, overexpression of miR-23a/b-3p in Hep1-6 cells elevated the intracellular triglyceride level and upregulated the expression of Srebp-1c and Fas. Taken together, these results suggested that miR-23a/b-3p enhanced mRNA stability by binding the 5'-UTR of Srebp-1c and Fas mRNA, thereby promoting triglyceride accumulation in hepatocytes.

miR-23a/b-3p通过调节Srebp-1c和Fas促进肝脏脂质积累。
miR-23a-3p和miR-23b-3p是miR-23~27~24-2超家族的成员。miR-23a/b-3p在调节肝脏脂质积累中的作用尚不清楚。在这里,我们发现miR-23a-3p和miR-23b-3p水平的升高伴随着高脂肪饮食小鼠和瘦素受体缺陷型2型糖尿病小鼠脂肪化肝脏中胆固醇调节元件结合蛋白-1 (SREBP-1)和脂肪酸合成酶(FAS)蛋白水平的升高(db/db)。重要的是,Hep1-6细胞中miR-23a/b-3p的过表达升高了细胞内甘油三酯水平,上调了Srebp-1c和Fas的表达。综上所述,这些结果表明miR-23a/b-3p通过结合Srebp-1c和Fas mRNA的5'-UTR增强mRNA的稳定性,从而促进甘油三酯在肝细胞中的积累。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of molecular endocrinology
Journal of molecular endocrinology 医学-内分泌学与代谢
CiteScore
6.90
自引率
0.00%
发文量
96
审稿时长
1 months
期刊介绍: The Journal of Molecular Endocrinology is an official journal of the Society for Endocrinology and is endorsed by the European Society of Endocrinology and the Endocrine Society of Australia. Journal of Molecular Endocrinology is a leading global journal that publishes original research articles and reviews. The journal focuses on molecular and cellular mechanisms in endocrinology, including: gene regulation, cell biology, signalling, mutations, transgenics, hormone-dependant cancers, nuclear receptors, and omics. Basic and pathophysiological studies at the molecule and cell level are considered, as well as human sample studies where this is the experimental model of choice. Technique studies including CRISPR or gene editing are also encouraged.
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