Mesenchymal Wnt signaling promotes formation of sternum and thoracic body wall

Dev Biol. 2015 May 15;401(2):264-75. doi: 10.1016/j.ydbio.2015.02.014. Epub 2015 Feb 26.


Midline defects account for approximately 5% of congenital abnormalities observed at birth. However, the molecular mechanisms underlying the formation of the ventral body wall are not well understood. Recent studies linked mutations in Porcupine-an O-acetyl transferase mediating Wnt ligand acylation-with defects in the thoracic body wall. We hypothesized that anomalous Wnt signaling is involved in the pathogenesis of defective closure of the thoracic body wall. We generated a mouse model wherein Wntless (Wls), which encodes a cargo receptor mediating secretion of Wnt ligands, was conditionally deleted from the developing mesenchyme using Dermo1Cre mice. Wls(f/f);Dermo1(Cre/+) embryos died during mid-gestation. At E13.5, skeletal defects were observed in the forelimbs, jaw, and rib cage. At E14.5, midline defects in the thoracic body wall began to emerge: the sternum failed to fuse and the heart protruded through the body wall at the midline (ectopia cordis). To determine the molecular mechanism underlying the phenotype observed in Wls(f/f);Dermo1(Cre/+) embryos, we tested whether Wnt/β-catenin signaling was operative in developing the embryonic ventral body wall using Axin2(LacZ) and BatGal reporter mice. While Wnt/β-catenin signaling activity was observed at the midline of the ventral body wall before sternal fusion, this pattern of activity was altered and scattered throughout the body wall after mesenchymal deletion of Wls. Mesenchymal cell migration was disrupted in Wls(f/f);Dermo1(Cre/+) thoracic body wall partially due to anomalous β-catenin independent Wnt signaling as determined by in vitro assays. Deletion of Lrp5 and Lrp6 receptors, which mediate Wnt/β-catenin signaling in the mesenchyme, partially recapitulated the phenotype observed in the chest midline of Wls(f/f);Dermo1(Cre/+) embryos supporting a role for Wnt/β-catenin signaling activity in the normal formation of the ventral body wall mesenchyme. We conclude that Wls-mediated secretion of Wnt ligands from the developing ventral body wall mesenchyme plays a critical role in fusion of the sternum and closure of the secondary body wall. Thus, impaired Wls activity in the ventral body wall mesenchyme is a mechanism underlying ectopia cordis and unfused sternum.

Keywords: Midline defects; Pentalogy of Cantrell; Sternum; Wls; ectopia cordis.

Publication types

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

MeSH terms

  • Acyltransferases
  • Animals
  • Axin Protein / genetics
  • Cell Movement / genetics
  • Cell Proliferation
  • Cells, Cultured
  • Ectopia Cordis / genetics
  • Gene Expression Regulation, Developmental
  • Intracellular Signaling Peptides and Proteins / genetics*
  • Low Density Lipoprotein Receptor-Related Protein-5 / genetics
  • Low Density Lipoprotein Receptor-Related Protein-6 / genetics
  • Membrane Proteins / genetics
  • Mesoderm / embryology*
  • Mesoderm / metabolism
  • Mice
  • Mice, Knockout
  • Neural Tube Defects / genetics
  • Receptors, G-Protein-Coupled / genetics*
  • Sternum / embryology*
  • Thoracic Cavity / embryology*
  • Wnt Proteins / genetics*
  • Wnt Signaling Pathway / genetics
  • beta Catenin / genetics


  • Axin Protein
  • Axin2 protein, mouse
  • Gpr177 protein, mouse
  • Intracellular Signaling Peptides and Proteins
  • Low Density Lipoprotein Receptor-Related Protein-5
  • Low Density Lipoprotein Receptor-Related Protein-6
  • Lrp5 protein, mouse
  • Lrp6 protein, mouse
  • Membrane Proteins
  • Receptors, G-Protein-Coupled
  • Wnt Proteins
  • beta Catenin
  • Acyltransferases
  • Porcn protein, mouse