Patterns of Wnt pathway activity in the mouse incisor indicate absence of Wnt/beta-catenin signaling in the epithelial stem cells

Dev Dyn. 2010 Jan;239(1):364-72. doi: 10.1002/dvdy.22106.

Abstract

The Wnt pathway is crucial for tooth development as shown by dental defects caused by impaired Wnt signaling in mouse and human. We investigated Wnt signaling in continuously growing mouse incisors focusing on epithelial stem cells. Ten Wnt ligands were expressed both in the dental epithelium and mesenchyme, and were associated mainly with odontoblast and ameloblast differentiation. Wnt/beta-catenin activity was detected in mesenchyme in BATgal and TOPgal reporter mice while Axin2, also a reporter of Wnt/beta-catenin signaling, was expressed additionally in the epithelium. Axin2 was, however, excluded from the epithelial stem cells in the cervical loop. Interestingly, these cells expressed specifically Lgr5, a Wnt target gene and stem cell marker in the intestine, suggesting that Lgr5 is a marker of incisor stem cells but is not regulated by Wnt signaling in the incisor. We conclude that epithelial stem cells in the mouse incisors are not regulated directly by Wnt/beta-catenin signaling.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Axin Protein
  • Biomarkers / metabolism
  • Cell Differentiation / physiology*
  • Cytoskeletal Proteins / metabolism
  • Epithelial Cells / metabolism*
  • In Situ Hybridization
  • Incisor / cytology
  • Incisor / growth & development*
  • Ligands
  • Mice
  • Receptors, G-Protein-Coupled / metabolism
  • Signal Transduction / physiology*
  • Stem Cells / metabolism*
  • Wnt Proteins / metabolism*
  • beta Catenin / metabolism*

Substances

  • Axin Protein
  • Axin2 protein, mouse
  • Biomarkers
  • Cytoskeletal Proteins
  • Lgr5 protein, mouse
  • Ligands
  • Receptors, G-Protein-Coupled
  • Wnt Proteins
  • beta Catenin