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Regulation of Calbindin-D28k Expression by Msx2 in the Dental Epithelium
Author(s) -
Alba Bolaños,
Dominique Hotton,
Didier Ferbus,
Sophia Loiodice,
Ariane Berdal,
Sylvie Babajko
Publication year - 2012
Publication title -
journal of histochemistry and cytochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.971
H-Index - 124
eISSN - 1551-5044
pISSN - 0022-1554
DOI - 10.1369/0022155412450641
Subject(s) - ameloblast , calbindin , amelogenin , amelogenesis , calcium binding protein , microbiology and biotechnology , biology , epithelium , calcium , chemistry , enamel paint , immunohistochemistry , gene , biochemistry , genetics , immunology , materials science , organic chemistry , composite material
Amelogenesis involves the coordinated expression of a set of molecules that includes enamel matrix proteins and calcium-binding proteins. Msx2 is a member of the divergent homeobox gene family and is instrumental in dental morphogenesis and biomineralization. This study focused on an EF-hand calcium-binding protein, calbindin-D 28k , which is highly expressed in dental epithelium. In vivo data showed that calbindin-D 28k levels were higher in ameloblasts from Msx2 +/− mice than Msx2 +/+ mice. Consistent with this finding, calbindin-D 28k distribution was affected in transgenic mice with ectopic expression in root epithelium in rests of Malassez in Msx2 +/− and more clearly in Msx2 −/− mice. In accordance with these in vivo data, calbindin-D 28k protein and mRNA levels were decreased in LS8 ameloblast-like cells by exogenous Msx2 overexpression. Furthermore, calbindin-D 28k promoter activity (nt-1075/+34) was specifically diminished in the presence of Msx2 overexpression, showing that Msx2 behave as a transcriptional repressor for calbindin-D 28k gene expression. In conclusion, Msx2 may control the spatiotemporally restricted frame of calbindin-D 28k production in the dental epithelium in relation to enamel mineralization, as previously shown for amelogenin.

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