Origin of non-cardiac endothelial cells from an Isl1+ lineage

FEBS Lett. 2012 Jun 21;586(13):1790-4. doi: 10.1016/j.febslet.2012.05.014. Epub 2012 May 18.

Abstract

The cardiovascular system consists of many cell types with distinct embryonic origins. Cells from an Islet1 (Isl1)-expressing progenitor population make a substantial contribution to the developing heart. We reasoned that cells derived from Isl1-expressing progenitors might contribute more widely to the cardiovascular system. We show that cells derived from an Isl1-expressing progenitor lineage make a wide contribution to the systemic vasculature and that embryos conditionally deficient for Rac1 within this cell population develop defects in the non-cardiac vasculature. These data define new roles for Isl1 in the developing embryo and demonstrate a contribution of Isl1-expressing progenitors to vascular endothelium in vivo.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cardiovascular System
  • Cell Differentiation
  • Cell Lineage*
  • Endothelial Cells / cytology*
  • Endothelial Cells / metabolism
  • Endothelium, Vascular / cytology
  • Endothelium, Vascular / metabolism
  • Gene Expression Regulation, Developmental
  • Heart / embryology
  • LIM-Homeodomain Proteins / genetics*
  • LIM-Homeodomain Proteins / metabolism
  • Mice
  • Mice, Inbred Strains
  • Myocardium / metabolism
  • Neuropeptides / genetics
  • Neuropeptides / metabolism
  • Stem Cells / cytology
  • Stem Cells / metabolism
  • Transcription Factors / genetics*
  • Transcription Factors / metabolism
  • rac GTP-Binding Proteins / genetics
  • rac GTP-Binding Proteins / metabolism
  • rac1 GTP-Binding Protein

Substances

  • LIM-Homeodomain Proteins
  • Neuropeptides
  • Rac1 protein, mouse
  • Transcription Factors
  • insulin gene enhancer binding protein Isl-1
  • rac GTP-Binding Proteins
  • rac1 GTP-Binding Protein