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

Author:

Li Linfang12,Zhang Xiaoyi2,Ren Hangjiang1,Huang Xiuqing2,Shen Tao2,Tang Weiqing2,Dou Lin2ORCID,Li Jian12

Affiliation:

1. 1Graduate School of Peking Union Medical College, Beijing, China

2. 2The Key Laboratory of Geriatrics, Beijing Institute of Geriatrics, Beijing Hospital, National Center of Gerontology, National Health Commission, Institute of Geriatric Medicine, Chinese Academy of Medical Sciences, Beijing, China

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.

Publisher

Bioscientifica

Subject

Endocrinology,Molecular Biology

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