Nfatc1 directs the endocardial progenitor cells to make heart valve primordium

Trends Cardiovasc Med. 2013 Nov;23(8):294-300. doi: 10.1016/j.tcm.2013.04.003. Epub 2013 May 10.

Abstract

Heart valves arise from the cardiac endocardial cushions located at the atrioventricular canal (AVC) and cardiac outflow tract (OFT) during development. A subpopulation of cushion endocardial cells undergoes endocardial to mesenchymal transformation (EMT) and generates the cushion mesenchyme, which is then remodeled into the interstitial tissue of the mature valves. The cushion endocardial cells that do not undertake EMT proliferate to elongate valve leaflets. During EMT and the post-EMT valve remodeling, endocardial cells at the cushions highly express nuclear factor in activated T cell, cytoplasmic 1 (Nfatc1), a transcription factor required for valve formation in mice. In this review, we present the current knowledge of Nfatc1 roles in the ontogeny of heart valves with a focus on the fate decision of the endocardial cells in the processes of EMT and valve remodeling.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Cell Differentiation / genetics
  • Endocardial Cushions / embryology*
  • Endocardium / embryology
  • Gene Expression Regulation, Developmental
  • Heart Valves / embryology*
  • Mesoderm / embryology
  • Mice
  • Models, Genetic
  • NFATC Transcription Factors / genetics*
  • Stem Cells / physiology
  • Transcription Elongation, Genetic

Substances

  • NFATC Transcription Factors
  • Nfatc1 protein, mouse