[The tooth: A marker of developmental abnormalities].

Med Sci (Paris)

FHU DDS Paris-Net, université Paris Cité, Inserm, AP-HP ; laboratoire BRIO URP2496, UFR d'odontologie ; AP-HP, hôpital Bretonneau ; centre de référence maladies Rares du métabolisme du calcium, phosphate et magnésium, filière OSCAR, European Reference Network BOND, Paris.

Published: January 2024

AI Article Synopsis

  • Tooth formation involves specific interactions between epithelial and mesenchymal tissues, and any anomalies may indicate underlying health issues in systems like the kidneys, bones, or nervous system.
  • The process of tooth development starts at three weeks of gestation, initiated by a signal from the PITX2 gene, and progresses through various stages influenced by multiple transcription factors and growth factors such as BMP, FGF, SHH, and WNT.
  • Disruptions in these developmental processes can lead to changes in tooth structure and shape, which should be considered in patient assessments and could help identify genetic abnormalities for better multidisciplinary treatment.

Article Abstract

Tooth formation results from specific epithelial-mesenchymal interactions, which summarize a number of developmental processes. Tooth anomalies may thus reflect subclinical diseases of the kidney, bone and more broadly of the mineral metabolism, skin or nervous system. Odontogenesis starts from the 3 week of intrauterine life by the odontogenic orientation of epithelial cells by a first PITX2 signal. The second phase is the acquisition of the number, shape, and position of teeth. It depends on multiple transcription and growth factors (BMP, FGF, SHH, WNT). These ecto-mesenchymal interactions guide cell migration, proliferation, apoptosis and differentiation ending in the formation of the specific dental mineralized tissues. Thus, any alteration will have consequences on the tooth structure or shape. Resulting manifestations will have to be considered in the patient phenotype and the multidisciplinary care, but also may contribute to identify the altered genetic circuity.

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Source
http://dx.doi.org/10.1051/medsci/2023190DOI Listing

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