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  4. The Absence of Claudin-10 in the Enamel Organ Alters Its Integrity
 
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2026
Journal Article
Title

The Absence of Claudin-10 in the Enamel Organ Alters Its Integrity

Abstract
Rare disorders related to tight junction (TJ) proteins have been associated with amelogenesis imperfecta. Pathogenic variants of , encoding claudin-10b, a cation transport pore, cause the autosomal recessive HELIX syndrome (Hypohidrosis, Electrolyte imbalance, hypoLacrymia, Ichthyosis, Xerostomia). Patients exhibit salivary dysfunction and rapid enamel wear after tooth eruption. Since C is expressed in the dental epithelium, this study explores the role of claudin-10b in amelogenesis. We analyzed amelogenesis in constitutive and conditional knockout (KO) murine models, comparing the findings to human HELIX enamel. First, analysis of constitutive knockout (KO) mice, which die within a few hours after birth, showed that claudin-10 is present at the plasma membrane of the stratum intermedium but not at the TJs during the secretory stage. Its absence altered gene expression related to ion transport and pH control, although without major disturbance in cell polarization or enamel matrix synthesis. Examination of later stages of amelogenesis in epithelium-targeted conditional KO mice showed that claudin-10 is present in the papillary layer at the maturation stage. In its absence, the pH of the enamel matrix was more basic during early maturation, suggesting that claudin-10 determines enamel matrix pH. However, at later stage of the maturation process, the pH was corrected and the resulting enamel did not show major structural or elemental alterations. These later findings were confirmed by exploring the enamel of KO transplanted tooth germs, which have developed in a controlled mineral environment. Nevertheless, higher contents of aluminum were detected in the enamel of transplanted germs and in human HELIX enamel, suggesting that claudin-10 deficiency may lead to a loss of enamel organ integrity. These data suggest that while salivary dysfunction is the main cause of enamel wear in HELIX, claudin-10 plays a direct role in amelogenesis by determining pH and enamel organ integrity.
Author(s)
Nguyen, T.N.
Ribes, S.
Andrique, C.
Requin, M.
Bouchet, J.
Obtel, N.
Slimani, L.
Brouilly, N.
Torrens, C.
Schmitt, A.
Guilbert, T.
Morawietz, Maria
Fraunhofer-Institut für Mikrostruktur von Werkstoffen und Systemen IMWS  
Kiesow, Andreas  
Fraunhofer-Institut für Mikrostruktur von Werkstoffen und Systemen IMWS  
Brunelle, A.
Percot, A.
Hadj-Rabia, S.
Gaucher, C.
Le Bivic, A
Houillier, P.
Bardet, C.
Muller, D.
Ramirez Rozzi, F.
Coradin, T.
Breiderhoff, T.
Chaussain, C.
Journal
Journal of dental research  
Open Access
DOI
10.1177/00220345251349109
Additional link
Full text
Language
English
Fraunhofer-Institut für Mikrostruktur von Werkstoffen und Systemen IMWS  
Keyword(s)
  • Aluminum

  • Ameloblasts

  • Amelogenesis

  • Genetic disorders

  • Ion transport

  • Tight junctions

  • Biomaterials

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