Heart valve development: endothelial cell signaling and differentiation

Circ Res. 2004 Sep 3;95(5):459-70. doi: 10.1161/01.RES.0000141146.95728.da.

Abstract

During the past decade, single gene disruption in mice and large-scale mutagenesis screens in zebrafish have elucidated many fundamental genetic pathways that govern early heart patterning and differentiation. Specifically, a number of genes have been revealed serendipitously to play important and selective roles in cardiac valve development. These initially surprising results have now converged on a finite number of signaling pathways that regulate endothelial proliferation and differentiation in developing and postnatal heart valves. This review highlights the roles of the most well-established ligands and signaling pathways, including VEGF, NFATc1, Notch, Wnt/beta-catenin, BMP/TGF-beta, ErbB, and NF1/Ras. Based on the interactions among and relative timing of these pathways, a signaling network model for heart valve development is proposed.

Publication types

  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Animals
  • Cell Differentiation
  • Endothelial Cells / cytology
  • Endothelial Cells / metabolism
  • Endothelium, Vascular / cytology
  • Endothelium, Vascular / embryology*
  • Endothelium, Vascular / growth & development
  • Endothelium, Vascular / metabolism
  • Heart Valves / cytology
  • Heart Valves / embryology*
  • Heart Valves / growth & development
  • Humans
  • Mice
  • Models, Cardiovascular*
  • Proteins / physiology
  • Signal Transduction*

Substances

  • Proteins