Simultaneous Fluorescent Identification of Odontoblasts and Ameloblasts.

J Dent Res

Department of Stem Cells and Developmental Biology, Division of Fundamental Medicine, Mie University Graduate School of Medicine, Tsu, Mie, Japan.

Published: May 2021

The tooth is mainly composed of dentin and enamel. Identification of dentin-producing odontoblasts and enamel-producing ameloblasts using reporter techniques is useful to study tooth development and regeneration with tissue engineering. Ameloblasts express , and , whereas odontoblasts express () and (). Although there are several transgenic lines using promoter elements or bacterial artificial chromosomes (BACs) to label odontoblasts and ameloblasts, there is a possibility that the expression patterns vary from the endogenous genes. Here, we established 2 lines of mice where tdTomato was knocked into the second exon of X-chromosomal (), and green fluorescent protein (GFP) was knocked into the second exon of . tdTomato and GFP were highly expressed on secretory ameloblasts and secretory and fully differentiated odontoblasts, respectively. In addition, DSPP and AMELX were not produced in the dentin matrix and enamel matrix of and male mice (as representative of hemizygous male mice), respectively. Moreover, micro-computed tomography analysis of male mice revealed a notable reduction in enamel volume but increased dentin mineral density. mice had reduced dentin mineral density. To identify odontoblasts and ameloblasts from developing tooth, we examined the expression of mesenchymal cell surface molecules CD90, CD166 and epithelial cell surface molecules CD49f, Epcam1 with fluorescence on odontoblasts and ameloblasts in these mice. We found that GFP odontoblasts and tdTomato ameloblasts in tooth germ from 0.5-d-old mice and male mice were enriched in CD45/Ter119/Epcam1/CD90/Integrin α4cell fractions and CD45/Ter119/Epcam1/CD49f/CD147 cell fractions, respectively. By using antibodies against mesenchymal and epithelial cell surface molecules and fluorescence, we can easily distinguish odontoblasts from ameloblasts and isolate each cell for further studies. These mice would serve as useful models for tooth development and regeneration as well as provide concurrent observation for the differentiation processes of odontoblasts and ameloblasts in vivo and in vitro.

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http://dx.doi.org/10.1177/0022034520974576DOI Listing

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