SHP-2 is required for the maintenance of cardiac progenitors

Development. 2007 Nov;134(22):4119-30. doi: 10.1242/dev.009290. Epub 2007 Oct 10.

Abstract

The isolation and culturing of cardiac progenitor cells has demonstrated that growth factor signaling is required to maintain cardiac cell survival and proliferation. In this study, we demonstrate in Xenopus that SHP-2 activity is required for the maintenance of cardiac precursors in vivo. In the absence of SHP-2 signaling, cardiac progenitor cells downregulate genes associated with early heart development and fail to initiate cardiac differentiation. We further show that this requirement for SHP-2 is restricted to cardiac precursor cells undergoing active proliferation. By demonstrating that SHP-2 is phosphorylated on Y542/Y580 and that it binds to FRS-2, we place SHP-2 in the FGF pathway during early embryonic heart development. Furthermore, we demonstrate that inhibition of FGF signaling mimics the cellular and biochemical effects of SHP-2 inhibition and that these effects can be rescued by constitutively active/Noonan-syndrome-associated forms of SHP-2. Collectively, these results show that SHP-2 functions within the FGF/MAPK pathway to maintain survival of proliferating populations of cardiac progenitor cells.

Publication types

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

MeSH terms

  • Animals
  • Branchial Region / embryology
  • Branchial Region / metabolism
  • Cell Death / drug effects
  • Cell Proliferation*
  • Cell Survival
  • Embryo, Nonmammalian
  • Fibroblast Growth Factors / physiology
  • Heart / drug effects
  • Heart / embryology
  • Heart / physiology*
  • Mesoderm / embryology
  • Mesoderm / metabolism
  • Models, Biological
  • Myocardium / cytology
  • Myocardium / enzymology
  • Myocardium / metabolism
  • Myocytes, Cardiac / drug effects
  • Myocytes, Cardiac / metabolism
  • Myocytes, Cardiac / physiology
  • Myosin Heavy Chains / metabolism
  • Organ Culture Techniques
  • Protein Tyrosine Phosphatase, Non-Receptor Type 11 / antagonists & inhibitors
  • Protein Tyrosine Phosphatase, Non-Receptor Type 11 / metabolism
  • Protein Tyrosine Phosphatase, Non-Receptor Type 11 / physiology*
  • Quinolines / pharmacology
  • Signal Transduction
  • Stem Cells / enzymology
  • Stem Cells / physiology*
  • Xenopus laevis / embryology

Substances

  • NSC-87877
  • Quinolines
  • Fibroblast Growth Factors
  • Protein Tyrosine Phosphatase, Non-Receptor Type 11
  • Myosin Heavy Chains