An interaction between MKL1, BRG1, and C/EBPβ mediates palmitate induced CRP transcription in hepatocytes

Biochim Biophys Acta Gene Regul Mech. 2019 Sep;1862(9):194412. doi: 10.1016/j.bbagrm.2019.194412. Epub 2019 Jul 26.

Abstract

Non-alcoholic steatohepatitis (NASH) is one of the most predominant disorders in metabolic syndrome. Induction of pro-inflammatory mediators in hepatocytes exposed to free fatty acids represents a hallmark event during NASH pathogenesis. C-reactive protein (CRP) is a prototypical pro-inflammatory mediator. In the present study, we investigated the mechanism by which megakaryocytic leukemia 1 (MKL1) mediates palmitate (PA) induced CRP transcription in hepatocytes. We report that over-expression of MKL1, but not MKL2, activated the CRP promoter whereas depletion or inhibition of MKL1 repressed the CRP promoter. MKL1 potentiated the induction of the CRP promoter activity by PA treatment. Importantly, MKL1 knockdown by siRNA or pharmaceutical inhibition by CCG-1423 attenuated the induction of endogenous CRP expression in hepatocytes. Similarly, primary hepatocytes isolated from wild type (WT) mice produced more CRP than those isolated from MKL1 deficient (KO) mice when stimulated with PA. Mechanistically, the sequence-specific transcription factor CCAAT-enhancer-binding protein (C/EBPβ) interacted with MKL1 and recruited MKL1 to activate CRP transcription. Reciprocally, MKL1 modulated C/EBPβ activity by recruiting the chromatin remodeling protein BRG1 to the CRP promoter to alter histone modifications. In conclusion, our data delineate a novel epigenetic mechanism underlying augmented hepatic inflammation during NASH pathogenesis.

Keywords: Epigenetics; Hepatocyte; Inflammation; Transcriptional regulation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • C-Reactive Protein / chemistry
  • C-Reactive Protein / genetics*
  • CCAAT-Enhancer-Binding Protein-beta / chemistry
  • CCAAT-Enhancer-Binding Protein-beta / genetics*
  • Chromatin Assembly and Disassembly / genetics
  • DNA Helicases / genetics*
  • Gene Expression Regulation / genetics
  • Hep G2 Cells
  • Hepatocytes / metabolism
  • Humans
  • Mice
  • Mice, Knockout
  • Non-alcoholic Fatty Liver Disease / genetics*
  • Non-alcoholic Fatty Liver Disease / pathology
  • Nuclear Proteins / genetics*
  • Promoter Regions, Genetic
  • Trans-Activators / chemistry
  • Trans-Activators / genetics*
  • Transcription Factors / genetics*

Substances

  • CCAAT-Enhancer-Binding Protein-beta
  • CEBPB protein, human
  • MRTFA protein, human
  • MRTFB protein, human
  • Nuclear Proteins
  • Trans-Activators
  • Transcription Factors
  • C-Reactive Protein
  • SMARCA4 protein, human
  • DNA Helicases