| Literature DB >> 26426912 |
Claire Bardet1, Frédéric Courson2, Yong Wu1,3, Mayssam Khaddam1, Benjamin Salmon1,2, Sandy Ribes1, Julia Thumfart4, Paulo M Yamaguti5, Gael Y Rochefort1, Marie-Lucile Figueres6, Tilman Breiderhoff4, Alejandro Garcia-Castaño7, Benoit Vallée8, Dominique Le Denmat1, Brigitte Baroukh1, Thomas Guilbert9, Alain Schmitt10, Jean-Marc Massé10, Dominique Bazin11, Georg Lorenz12, Maria Morawietz12, Jianghui Hou13, Patricia Carvalho-Lobato14, Maria Cristina Manzanares14, Jean-Christophe Fricain15, Deborah Talmud16, Renato Demontis17, Francisco Neves18, Delphine Zenaty19, Ariane Berdal6, Andreas Kiesow12, Matthias Petzold12, Suzanne Menashi8, Agnes Linglart20, Ana Carolina Acevedo5, Rosa Vargas-Poussou7, Dominik Müller4, Pascal Houillier6,21, Catherine Chaussain1,2.
Abstract
Claudin-16 protein (CLDN16) is a component of tight junctions (TJ) with a restrictive distribution so far demonstrated mainly in the kidney. Here, we demonstrate the expression of CLDN16 also in the tooth germ and show that claudin-16 gene (CLDN16) mutations result in amelogenesis imperfecta (AI) in the 5 studied patients with familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC). To investigate the role of CLDN16 in tooth formation, we studied a murine model of FHHNC and showed that CLDN16 deficiency led to altered secretory ameloblast TJ structure, lowering of extracellular pH in the forming enamel matrix, and abnormal enamel matrix protein processing, resulting in an enamel phenotype closely resembling human AI. This study unravels an association of FHHNC owing to CLDN16 mutations with AI, which is directly related to the loss of function of CLDN16 during amelogenesis. Overall, this study indicates for the first time the importance of a TJ protein in tooth formation and underlines the need to establish a specific dental follow-up for these patients.Entities:
Keywords: AMELOGENESIS IMPERFECTA (AI); FAMILIAL HYPOMAGNESEMIA WITH HYPERCALCIURIA AND NEPHROCALCINOSIS (FHHNC); MMP-20; SECRETORY AMELOBLASTS; pH
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Year: 2015 PMID: 26426912 DOI: 10.1002/jbmr.2726
Source DB: PubMed Journal: J Bone Miner Res ISSN: 0884-0431 Impact factor: 6.741