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Specificity Protein 7 Is Required for Proliferation and Differentiation of Ameloblasts and Odontoblasts.
- Source :
-
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research [J Bone Miner Res] 2018 Jun; Vol. 33 (6), pp. 1126-1140. Date of Electronic Publication: 2018 Mar 24. - Publication Year :
- 2018
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Abstract
- The Sp7/Osterix transcription factor is essential for bone development. Mutations of the Sp7 gene in humans are associated with craniofacial anomalies and osteogenesis imperfecta. However, the role of Sp7 in embryonic tooth development remains unknown. Here we identified the functional requirement of Sp7 for dentin synthesis and tooth development. Sp7-null mice exhibit craniofacial dysmorphogenesis and are completely void of alveolar bone. Surprisingly, initial tooth morphogenesis progressed normally in Sp7-null mice. Thus the formation of alveolar bone is not a prerequisite for tooth morphogenesis. Sp7 is required for mineralization of palatal tissue but is not essential for palatal fusion. The reduced proliferative capacity of Sp7-deficient ectomesenchyme results in small and misshapen teeth with randomly arranged cuboidal preodontoblasts and preameloblasts. Sp7 promotes functional maturation and polarization of odontoblasts. Markers of mature odontoblast (Col1a, Oc, Dspp, Dmp1) and ameloblast (Enam, Amelx, Mmp20, Amtn, Klk4) are barely expressed in incisors and molar tissues of Sp7-null mice. Consequently, dentin and enamel matrix are absent in the Sp7-null littermates. Interestingly, the Sp7 expression is restricted to cells of the dental mesenchyme indicating the effect on oral epithelium-derived ameloblasts is cell-nonautonomous. Abundant expression of Fgf3 and Fgf8 ligand was noted in the developing tooth of wild-type mice. Both ligands were remarkably absent in the Sp7-null incisor and molar, suggesting cross-signaling between mesenchyme and epithelium is disrupted. Finally, promoter-reporter assays revealed that Sp7 directly controls the expression of Fgf-ligands. Together, our data demonstrate that Sp7 is obligatory for the differentiation of both ameloblasts and odontoblasts but not for the initial tooth morphogenesis. © 2018 American Society for Bone and Mineral Research.<br /> (© 2018 American Society for Bone and Mineral Research.)
- Subjects :
- Animals
Animals, Newborn
Calcification, Physiologic
Cell Proliferation
Collagen metabolism
Dentin metabolism
Embryonic Development
Fibroblast Growth Factors metabolism
Gene Expression Regulation
Incisor growth & development
Incisor metabolism
Incisor ultrastructure
Mesoderm metabolism
Mice, Inbred C57BL
Morphogenesis
Palate metabolism
Signal Transduction
Sp7 Transcription Factor deficiency
Sp7 Transcription Factor genetics
Stem Cells metabolism
Ameloblasts cytology
Ameloblasts metabolism
Cell Differentiation
Odontoblasts cytology
Odontoblasts metabolism
Sp7 Transcription Factor metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1523-4681
- Volume :
- 33
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
- Publication Type :
- Academic Journal
- Accession number :
- 29405385
- Full Text :
- https://doi.org/10.1002/jbmr.3401