The actin-MRTF-SRF gene regulatory axis and myofibroblast differentiation

J Cardiovasc Transl Res. 2012 Dec;5(6):794-804. doi: 10.1007/s12265-012-9397-0. Epub 2012 Aug 17.


Cardiac fibroblasts are responsible for necrotic tissue replacement and scar formation after myocardial infarction (MI) and contribute to remodeling in response to pathological stimuli. This response to insult or injury is largely due to the phenotypic plasticity of fibroblasts. When fibroblasts encounter environmental disturbances, whether biomechanical or humoral, they often transform into smooth muscle-like, contractile cells called "myofibroblasts." The signals that control myofibroblast differentiation include the transforming growth factor (TGF)-β1-Smad pathway and Rho GTPase-dependent actin polymerization. Recent evidence implicates serum response factor (SRF) and the myocardin-related transcription factors (MRTFs) as key mediators of the contractile gene program in response to TGF-β1 or RhoA signaling. This review highlights the function of myofibroblasts in cardiac remodeling and the role of the actin-MRTF-SRF signaling axis in regulating this process.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Actins / metabolism*
  • Animals
  • Cell Differentiation* / genetics
  • Fibrosis
  • Gene Expression Regulation
  • Heart Diseases / genetics
  • Heart Diseases / metabolism*
  • Heart Diseases / pathology
  • Heart Diseases / therapy
  • Humans
  • Myocardium / metabolism*
  • Myocardium / pathology
  • Myofibroblasts / metabolism*
  • Myofibroblasts / pathology
  • Phenotype
  • Serum Response Factor / metabolism*
  • Signal Transduction
  • Transcription Factors / metabolism*


  • Actins
  • Serum Response Factor
  • Transcription Factors