Multipotent flk-1+ cardiovascular progenitor cells give rise to the cardiomyocyte, endothelial, and vascular smooth muscle lineages

Dev Cell. 2006 Nov;11(5):723-32. doi: 10.1016/j.devcel.2006.10.002.

Abstract

Cell-tracing studies in the mouse indicate that the cardiac lineage arises from a population that expresses the vascular endothelial growth factor receptor 2 (VEGFR2, Flk-1), suggesting that it may develop from a progenitor with vascular potential. Using the embryonic stem (ES) cell differentiation model, we have identified a cardiovascular progenitor based on the temporal expression of the primitive streak (PS) marker brachyury and Flk-1. Comparable progenitors could also be isolated from head-fold stage embryos. When cultured with cytokines known to function during cardiogenesis, individual cardiovascular progenitors generated colonies that displayed cardiomyocyte, endothelial, and vascular smooth muscle (VSM) potential. Isolation and characterization of this previously unidentified population suggests that the mammalian cardiovascular system develops from multipotential progenitors.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Cardiovascular System / cytology
  • Cardiovascular System / embryology
  • Cell Differentiation
  • Cell Lineage
  • Cells, Cultured
  • Embryonic Stem Cells / cytology*
  • Endothelial Cells / cytology*
  • Fetal Proteins / metabolism
  • Mice
  • Multipotent Stem Cells / cytology*
  • Muscle, Smooth, Vascular / cytology*
  • Myocytes, Cardiac / cytology*
  • T-Box Domain Proteins / metabolism
  • Transcription Factors / biosynthesis
  • Vascular Endothelial Growth Factor Receptor-2 / metabolism*

Substances

  • Fetal Proteins
  • T-Box Domain Proteins
  • Transcription Factors
  • Vascular Endothelial Growth Factor Receptor-2
  • Brachyury protein