Early perturbation of Wnt signaling reveals patterning and invagination-evagination control points in molar tooth development
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural
Grantová podpora
BB/L002965/1
Biotechnology and Biological Sciences Research Council - United Kingdom
F30 DE025160
NIDCR NIH HHS - United States
R01 DE028496
NIDCR NIH HHS - United States
R35 DE026602
NIDCR NIH HHS - United States
PubMed
34195802
PubMed Central
PMC8326921
DOI
10.1242/dev.199685
PII: 270762
Knihovny.cz E-zdroje
- Klíčová slova
- Epithelial invagination, Morphogenesis, Mouse, Tooth development, Wnt signaling,
- MeSH
- beta-katenin metabolismus MeSH
- epitel metabolismus MeSH
- epitelové buňky cytologie metabolismus MeSH
- mezoderm metabolismus MeSH
- moláry cytologie růst a vývoj metabolismus MeSH
- morfogeneze fyziologie MeSH
- myši MeSH
- odontogeneze genetika fyziologie MeSH
- proliferace buněk MeSH
- signální dráha Wnt fyziologie MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Research Support, N.I.H., Extramural MeSH
- Názvy látek
- beta-katenin MeSH
- CTNNB1 protein, mouse MeSH Prohlížeč
Tooth formation requires complex signaling interactions both within the oral epithelium and between the epithelium and the underlying mesenchyme. Previous studies of the Wnt/β-catenin pathway have shown that tooth formation is partly inhibited in loss-of-function mutants, and gain-of-function mutants have perturbed tooth morphology. However, the stage at which Wnt signaling is first important in tooth formation remains unclear. Here, using an Fgf8-promoter-driven, and therefore early, deletion of β-catenin in mouse molar epithelium, we found that loss of Wnt/β-catenin signaling completely deletes the molar tooth, demonstrating that this pathway is central to the earliest stages of tooth formation. Early expression of a dominant-active β-catenin protein also perturbs tooth formation, producing a large domed evagination at early stages and supernumerary teeth later on. The early evaginations are associated with premature mesenchymal condensation marker, and are reduced by inhibition of condensation-associated collagen synthesis. We propose that invagination versus evagination morphogenesis is regulated by the relative timing of epithelial versus mesenchymal cell convergence regulated by canonical Wnt signaling. Together, these studies reveal new aspects of Wnt/β-catenin signaling in tooth formation and in epithelial morphogenesis more broadly.
Centre for Craniofacial Regeneration and Biology King's College London London SE1 9RT UK
Institute of Molecular Genetics of the ASCR v v i Prumyslova 595 252 42 Vestec Czech Republic
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