MicroRNA-744/transforming growth factor β1 relationship regulates liver cirrhosis

Hepatol Int. 2019 Nov;13(6):814-825. doi: 10.1007/s12072-019-09993-w. Epub 2019 Oct 23.

Abstract

Background: MicroRNAs have added a new dimension to our understanding of liver cirrhosis (LC) and associated processes like the activation of hepatic stellate cells (HSCs).

Methods: Serum samples were collected from 40 LC patients and 30 healthy donors. CCl4-induced LC mouse model in vivo and in vitro human HSC LX-2 and murine HSC JS-1 cells were researched.

Results: The levels of serum microRNA (miR)-744 is inversely correlated with the severity of LC and is a reliable biomarker of LC. In CCl4-induced LC model, the abundance of miR-744 was reduced in both sera and livers compared with sham controls. Importantly, increasing miR-744 abundance with synthetic miR-744 Agomir alleviated liver fibrosis, a critical component of LC, while reducing miR-744 with Antagomir exacerbated it. To elucidate molecular mechanism underlying the suppressive role of miR-744 in LC, we observed that miR-744 and transforming growth factor β1 (TGFβ1) are inversely correlated in LC patients' sera as well as sera/livers from CCl4-induced LC mice. We demonstrated that miR-744 Agomir downregulated the expression of TGFβ1 and further confirmed that TGFβ1 mRNA was a bona fide miR-744 target in HSCs. Moreover, miR-744 Agomir reduced the degree of F-actin formation and cell proliferation while miR-744 Antagomir promoted these events, suggesting that miR-744 is a negative regulator of HSC activation.

Conclusions: MiR-744-led suppression in HSC activation is most likely through TGFβ1 because exogenous TGFβ1 nearly negated miR-744 Agomir's action. This study suggests that reduction of miR-744 is a reliable biomarker for LC and miR-744/TGFβ1 relationship is a key regulator of LC.

Keywords: Hepatic stellate cells; Liver cirrhosis; TGFβ1; miR-744; miRNA.

MeSH terms

  • Animals
  • Case-Control Studies
  • Cell Proliferation / drug effects*
  • Disease Models, Animal
  • Down-Regulation
  • Female
  • Humans
  • Liver Cirrhosis / metabolism*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • MicroRNAs / metabolism*
  • Middle Aged
  • Transforming Growth Factor beta1 / metabolism*

Substances

  • MIRN744 microRNA, human
  • MicroRNAs
  • Transforming Growth Factor beta1