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Hepatic miR-192-3p reactivation alleviates steatosis by targeting glucocorticoid receptor.
Wang, Zhangting; Miu, Kai-Kei; Zhang, Xueyan; Wan, Angel Tsz-Yau; Lu, Gang; Cheung, Hoi-Hung; Lee, Heung-Man; Kong, Alice Pik-Shan; Chan, Juliana Chung-Ngor; Chan, Wai-Yee.
Afiliação
  • Wang Z; School of Biomedical Sciences, Faculty of Medicine, Chinese University of Hong Kong, Hong Kong Special Administrative Region, China.
  • Miu KK; School of Biomedical Sciences, Faculty of Medicine, Chinese University of Hong Kong, Hong Kong Special Administrative Region, China.
  • Zhang X; School of Biomedical Sciences, Faculty of Medicine, Chinese University of Hong Kong, Hong Kong Special Administrative Region, China.
  • Wan AT; Department of Gynecology, Women's Hospital, School of Medicine, Zhejiang University, Zhejiang, China.
  • Lu G; School of Biomedical Sciences, Faculty of Medicine, Chinese University of Hong Kong, Hong Kong Special Administrative Region, China.
  • Cheung HH; School of Biomedical Sciences, Faculty of Medicine, Chinese University of Hong Kong, Hong Kong Special Administrative Region, China.
  • Lee HM; School of Biomedical Sciences, Faculty of Medicine, Chinese University of Hong Kong, Hong Kong Special Administrative Region, China.
  • Kong AP; Department of Medicine and Therapeutics, Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong Special Administrative Region, China.
  • Chan JC; Department of Medicine and Therapeutics, Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong Special Administrative Region, China.
  • Chan WY; Hong Kong Institute of Diabetes and Obesity, Prince of Wales Hospital, Hong Kong Special Administrative Region, China.
JHEP Rep ; 2(6): 100179, 2020 Dec.
Article em En | MEDLINE | ID: mdl-33134908
BACKGROUND & AIMS: The paradox of hepatic insulin resistance describes the inability for liver to respond to bioenergetics hormones in suppressing gluconeogenesis whilst maintaining lipid synthesis. Here, we report the deficiency of miR-192-3p in the livers of mice with diabetes and its role in alleviating hepatic steatosis. METHODS: As conventional pre-microRNA (miRNA) stem-loop overexpression only boosts guiding strand (i.e. miR-192-5p) expression, we adopted an artificial AAV(DJ)-directed, RNA Pol III promoter-driven miRNA hairpin construct for star-strand-specific overexpression in the liver. Liver steatosis and insulin resistance markers were evaluated in primary hepatocytes, mice with diabetes, and mice with excessive carbohydrate consumption. RESULTS: Functional loss of miR-192-3p in liver exacerbated hepatic micro-vesicular steatosis and insulin resistance in either mice with diabetes or wild-type mice with excessive fructose consumption. Liver-specific overexpression of miR-192-3p effectively halted hepatic steatosis and ameliorated insulin resistance in these mice models. Likewise, hepatocytes overexpressing miR-192-3p exhibited improved lipid accumulation, accompanied with decreases in lipogenesis and lipid-accumulation-related transcripts. Mechanistically, glucocorticoid receptor (GCR, also known as nuclear receptor subfamily 3, group C, member 1 [NR3C1]) was demonstrated to be negatively regulated by miR-192-3p. The effect of miR-192-3p on mitigating micro-vesicular steatosis was ablated by the reactivation of NR3C1. CONCLUSIONS: The star strand miR-192-3p was an undermined glycerolipid regulator involved in controlling fat accumulation and insulin sensitivity in liver through blockade of hepatic GCR signalling; this miRNA may serve as a potential therapeutic option for the common co-mobility of diabetic mellitus and fatty liver disease. LAY SUMMARY: The potential regulatory activity of star strand microRNA (miRNA) species has been substantially underestimated. In this study, we investigate the role and mechanism of an overlooked star strand miRNA (miR-192-3p) in regulating hepatic steatosis and insulin signalling in the livers of mice with diabetes and mice under excessive carbohydrate consumption.
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Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: JHEP Rep Ano de publicação: 2020 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: JHEP Rep Ano de publicação: 2020 Tipo de documento: Article País de afiliação: China