Platelet-derived growth factor receptor alpha subunit deleted Patch mouse exhibits severe cardiovascular dysmorphogenesis

Authors

  • Gina C. Schatteman,

    Corresponding author
    1. Department of Pathology, University of Washington, Seattle, Washington 98195
    Current affiliation:
    1. Department of Cardiovascular Research, St. Elizabeth's Medical Center, Tufts University School of Medicine, 736 Cambridge Street, Boston, MA 02135
    • Department of Pathology, University of Washington, Seattle, Washington 98195
    Search for more papers by this author
  • S. Tim Motley,

    1. Department of Radiology, Children's Hospital and Medical Center, Seattle, Washington 98105
    Search for more papers by this author
  • Eric L. Effmann,

    1. Department of Radiology, Children's Hospital and Medical Center, Seattle, Washington 98105
    Search for more papers by this author
  • Daniel F. Bowen-Pope

    1. Department of Pathology, University of Washington, Seattle, Washington 98195
    Search for more papers by this author

Abstract

Path (Ph) mice, whose platelet-derived growth factor receptor alpha subunit (αPDGFR) gene has been deleted, have been used to elucidate requirements for αPDGFR for normal murine development. In this report we evaluate the role of αPDGFR in cardiovascular development by using in situ hybridization to follow the changing pattern of αPDGFR expression in cardiovascular tissues after embryonic day 13, and comparing this pattern with the pattern of cardiovascular defects observed in homozygous Ph mutants. Both mesodermally derived and neural crest-derived components of the cardiovascular system are severely dysmorphic in Ph/Ph embryos and those structures most severely affected are those that normally express αPDGFR mRNA at the highest levels and for the longest duration. Ph/Ph vessels appear to be lined with a normal endothelium, but contain a reduced number of smooth muscle cells and are fragile during processing for histology. The myocardium is thin, the heart is small and dysmorphic, the valves are malformed, and the interventricular and interatrial septa of the heart are defective. In the outflow tract, the spectrum of defects includes both persistent truncus arteriosus and double outlet right ventricle. This pattern of abnormalities is consistent with the hypothesis that deletion of αPDGFR results in a functional ablation of cranial neural crest cells, and that mesodermally derived components of the vascular system also require αPDGFR. © 1995 Wiley-Liss, Inc.

Ancillary