IGF signaling directs ventricular cardiomyocyte proliferation during embryonic heart development

Development. 2011 May;138(9):1795-805. doi: 10.1242/dev.054338. Epub 2011 Mar 23.

Abstract

Secreted factors from the epicardium are believed to be important in directing heart ventricular cardiomyocyte proliferation and morphogenesis, although the specific factors involved have not been identified or characterized adequately. We found that IGF2 is the most prominent mitogen made by primary mouse embryonic epicardial cells and by a newly derived immortalized mouse embryonic epicardial cell line called MEC1. In vivo, Igf2 is expressed in the embryonic mouse epicardium during midgestation heart development. Using a whole embryo culture assay in the presence of inhibitors, we confirmed that IGF signaling is required to activate the ERK proliferation pathway in the developing heart, and that the epicardium is required for this response. Global disruption of the Igf2 gene, or conditional disruption of the two IGF receptor genes Igf1r and Insr together in the myocardium, each resulted in a significant decrease in ventricular wall proliferation and in ventricular wall hypoplasia. Ventricular cardiomyocyte proliferation in mutant embryos was restored to normal at E14.5, concurrent with the establishment of coronary circulation. Our results define IGF2 as a previously unexplored epicardial mitogen that is required for normal ventricular chamber development.

Publication types

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

MeSH terms

  • Animals
  • Cell Proliferation* / drug effects
  • Cells, Cultured
  • Embryo, Mammalian
  • Gene Expression Regulation, Developmental / drug effects
  • Heart / drug effects
  • Heart / embryology*
  • Heart Ventricles / cytology
  • Heart Ventricles / metabolism
  • Insulin-Like Growth Factor II / genetics
  • Insulin-Like Growth Factor II / metabolism
  • Insulin-Like Growth Factor II / pharmacology
  • Insulin-Like Growth Factor II / physiology*
  • Mice
  • Mice, Inbred ICR
  • Mice, Transgenic
  • Myocardium / metabolism
  • Myocytes, Cardiac / drug effects
  • Myocytes, Cardiac / metabolism
  • Myocytes, Cardiac / physiology*
  • RNA, Small Interfering / pharmacology
  • Receptor, IGF Type 2 / genetics
  • Receptor, IGF Type 2 / metabolism
  • Receptor, IGF Type 2 / physiology
  • Signal Transduction / drug effects
  • Signal Transduction / genetics
  • Signal Transduction / physiology

Substances

  • RNA, Small Interfering
  • Receptor, IGF Type 2
  • Insulin-Like Growth Factor II