The β-catenin pathway contributes to the effects of leptin on SREBP-1c expression in rat hepatic stellate cells and liver fibrosis

Br J Pharmacol. 2013 May;169(1):197-212. doi: 10.1111/bph.12114.

Abstract

Background and purpose: Liver fibrosis is commonly associated with obesity and most obese patients develop hyperleptinaemia. The adipocytokine leptin has a unique role in the development of liver fibrosis. Activation of hepatic stellate cells (HSCs) is a key step in hepatic fibrogenesis and sterol regulatory element-binding protein-1c (SREBP-1c) can inhibit HSC activation. We have shown that leptin strongly inhibits SREBP-1c expression in rat HSCs. Hence, we aimed to clarify whether the β-catenin pathway, the crucial negative regulator of adipocyte differentiation, mediates the effects of leptin on SREBP-1c expression in HSCs and in mouse liver fibrosis.

Experimental approach: HSCs were prepared from rats and mice. Gene expressions were analysed by real-time PCR, Western blot analysis, immunostaining and transient transfection assays.

Key results: Leptin increased β-catenin protein but not mRNA levels in cultured HSCs. Leptin induced phosphorylation of glycogen synthase kinase-3β at Ser(9) and subsequent stabilization of β-catenin protein was mediated, at least in part, by ERK and p38 MAPK pathways. The leptin-induced β-catenin pathway reduced SREBP-1c expression and activity but did not affect protein levels of key regulators controlling SREBP-1c activity, and was not involved in leptin inhibition of liver X receptor α. In a mouse model of liver injury, the β-catenin pathway was shown to be involved in leptin-induced liver fibrosis.

Conclusions and implications: The β-catenin pathway contributes to leptin regulation of SREBP-1c expression in HSCs and leptin-induced liver fibrosis in mice. These results have potential implications for clarifying the mechanisms of liver fibrogenesis associated with elevated leptin levels.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Western
  • Disease Models, Animal
  • Gene Expression Regulation
  • Hepatic Stellate Cells / metabolism
  • Leptin / administration & dosage
  • Leptin / metabolism*
  • Liver Cirrhosis / pathology*
  • Liver X Receptors
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Orphan Nuclear Receptors / antagonists & inhibitors
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Real-Time Polymerase Chain Reaction
  • Sterol Regulatory Element Binding Protein 1 / genetics*
  • beta Catenin / metabolism*
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • Leptin
  • Liver X Receptors
  • Nr1h3 protein, mouse
  • Nr1h3 protein, rat
  • Orphan Nuclear Receptors
  • RNA, Messenger
  • Sterol Regulatory Element Binding Protein 1
  • beta Catenin
  • p38 Mitogen-Activated Protein Kinases