MicroRNA-155 Deficiency Attenuates Liver Steatosis and Fibrosis without Reducing Inflammation in a Mouse Model of Steatohepatitis

PLoS One. 2015 Jun 4;10(6):e0129251. doi: 10.1371/journal.pone.0129251. eCollection 2015.

Abstract

Background & aim: MicroRNAs (miRs) regulate hepatic steatosis, inflammation and fibrosis. Fibrosis is the consequence of chronic tissue damage and inflammation. We hypothesized that deficiency of miR-155, a master regulator of inflammation, attenuates steatohepatitis and fibrosis.

Methods: Wild type (WT) and miR-155-deficient (KO) mice were fed methionine-choline-deficient (MCD) or -supplemented (MCS) control diet for 5 weeks. Liver injury, inflammation, steatosis and fibrosis were assessed.

Results: MCD diet resulted in steatohepatitis and increased miR-155 expression in total liver, hepatocytes and Kupffer cells. Steatosis and expression of genes involved in fatty acid metabolism were attenuated in miR-155 KO mice after MCD feeding. In contrast, miR-155 deficiency failed to attenuate inflammatory cell infiltration, nuclear factor κ beta (NF-κB) activation and enhanced the expression of the pro-inflammatory cytokines tumor necrosis factor alpha (TNFα) and monocyte chemoattractant protein-1 (MCP1) in MCD diet-fed mice. We found a significant attenuation of apoptosis (cleaved caspase-3) and reduction in collagen and α smooth muscle actin (αSMA) levels in miR-155 KO mice compared to WTs on MCD diet. In addition, we found attenuation of platelet derived growth factor (PDGF), a pro-fibrotic cytokine; SMAD family member 3 (Smad3), a protein involved in transforming growth factor-β (TGFβ) signal transduction and vimentin, a mesenchymal marker and indirect indicator of epithelial-to-mesenchymal transition (EMT) in miR-155 KO mice. Nuclear binding of CCAAT enhancer binding protein β (C/EBPβ) a miR-155 target involved in EMT was significantly increased in miR-155 KO compared to WT mice.

Conclusions: Our novel data demonstrate that miR-155 deficiency can reduce steatosis and fibrosis without decreasing inflammation in steatohepatitis.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • CCAAT-Enhancer-Binding Protein-beta / metabolism
  • Cell Nucleus / metabolism
  • Choline
  • Diet
  • Disease Models, Animal
  • Fatty Liver / complications*
  • Fatty Liver / genetics*
  • Female
  • Gene Expression Regulation
  • Inflammation / complications*
  • Lipid Metabolism / genetics
  • Lipopolysaccharides / pharmacology
  • Liver / pathology
  • Liver Cirrhosis / complications*
  • Liver Cirrhosis / genetics*
  • Methionine
  • Mice, Inbred C57BL
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Protein Binding
  • Smad3 Protein / metabolism
  • Tumor Necrosis Factor-alpha / metabolism
  • Vimentin / metabolism

Substances

  • CCAAT-Enhancer-Binding Protein-beta
  • Lipopolysaccharides
  • MicroRNAs
  • Mirn155 microRNA, mouse
  • Smad3 Protein
  • Tumor Necrosis Factor-alpha
  • Vimentin
  • Methionine
  • Choline