A crosstalk between chromatin remodeling and histone H3K4 methyltransferase complexes in endothelial cells regulates angiotensin II-induced cardiac hypertrophy

J Mol Cell Cardiol. 2015 May:82:48-58. doi: 10.1016/j.yjmcc.2015.02.010. Epub 2015 Feb 21.

Abstract

Angiotensin II (Ang II) induces cardiac hypertrophy and fibrosis in part by stimulating endothelin (ET-1) transcription. The involvement of the epigenetic machinery in this process is largely undefined. In the present study, we examined the epigenetic maneuvering underlying cardiac hypertrophy and fibrosis following ET-1 transactivation by Ang II. In response to Ang II stimulation, core components of the mammalian chromatin remodeling complex (Brahma-related gene 1, or Brg1, and Brahma or Brm) and histone H3K4 methylation complex (Ash2, absent, small, or homeotic discs 2, or Ash2 and WD domain repeat 5, or Wdr5) were recruited to the ET-1 promoter region in endothelial cells. Over-expression of Brg1/Brm or Ash2/Wdr5 enhanced while depletion of Brg1/Brm or Ash2/Wdr5 attenuated Ang II-induced ET-1 transactivation. Endothelial-specific knockdown of Brg1/Brm or Ash2/Wdr5 ameliorated cardiac hypertrophy both in vitro and in vivo. More important, Brg1/Brm interacted with Ash2/Wdr5 on the ET-1 promoter to catalyze H3K4 methylation. The crosstalk between Brg11/Brm and Ash2/Wdr5 was mediated by myocardin-related transcription factor A (MRTF-A). In conclusion, our data have unveiled an epigenetic complex that links ET-1 transactivation in endothelial cells to Ang II-induced cardiac hypertrophy and fibrosis.

Keywords: Cardiac hypertrophy; ET-1; Epigenetics; Transcriptional regulation; Vascular endothelial cell.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angiotensin II / metabolism*
  • Animals
  • Cardiomegaly / genetics*
  • Cardiomegaly / metabolism*
  • Cardiomegaly / pathology
  • Cell Line, Transformed
  • Chromatin Assembly and Disassembly*
  • DNA Helicases / metabolism
  • Disease Models, Animal
  • Endothelial Cells / metabolism*
  • Endothelin-1 / genetics
  • Endothelin-1 / metabolism
  • Histone Methyltransferases
  • Histone-Lysine N-Methyltransferase / metabolism*
  • Humans
  • Male
  • Mice
  • Nuclear Proteins / metabolism
  • Promoter Regions, Genetic
  • Protein Binding
  • Signal Transduction
  • Trans-Activators / metabolism
  • Transcription Factors / metabolism

Substances

  • Endothelin-1
  • MRTFA protein, human
  • Nuclear Proteins
  • SMARCA2 protein, human
  • Trans-Activators
  • Transcription Factors
  • Angiotensin II
  • Histone Methyltransferases
  • Histone-Lysine N-Methyltransferase
  • SMARCA4 protein, human
  • DNA Helicases