Department of Stem Cells and Developmental Biology, Division of Fundamental Medicine, Mie University Graduate School of Medicine, Tsu, Mie, Japan.
Support Unit for Animal Resources Development, Research Resources Division, RIKEN Center for Brain Science, Wako-shi, Saitama, Japan.
J Dent Res. 2021 May;100(5):532-541. doi: 10.1177/0022034520974576. Epub 2020 Dec 8.
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.
牙齿主要由牙本质和釉质组成。使用报告基因技术鉴定产生牙本质的成牙本质细胞和成釉质的成釉细胞有助于研究牙齿发育和组织工程再生。成釉细胞表达 , ,而成牙本质细胞表达 ()和 ()。虽然有几种使用启动子元件或细菌人工染色体(BACs)标记成牙本质细胞和成釉细胞的转基因系,但表达模式可能与内源性基因不同。在这里,我们建立了 2 条小鼠品系,其中 tdTomato 敲入 X 染色体的第二个外显子 (),绿色荧光蛋白(GFP)敲入第二个外显子 。tdTomato 和 GFP 分别在分泌期成釉细胞和分泌期和成牙本质细胞中高度表达。此外,DSPP 和 AMELX 分别不在 和 雄性小鼠(代表 半合子雄性小鼠)的牙本质基质和釉质基质中产生。此外, 雄性小鼠的微计算机断层扫描分析显示,釉质体积明显减少,但牙本质矿化密度增加。 雄性小鼠的牙本质矿化密度降低。为了鉴定发育中牙齿的成牙本质细胞和成釉细胞,我们在这些小鼠中检查了间充质细胞表面分子 CD90、CD166 和上皮细胞表面分子 CD49f、Epcam1 在成釉细胞和成牙本质细胞上的表达。我们发现,0.5 天龄 小鼠和 雄性小鼠牙胚中的 GFP 成牙本质细胞和 tdTomato 成釉细胞在 CD45/Ter119/Epcam1/CD90/Integrin α4 细胞群和 CD45/Ter119/Epcam1/CD49f/CD147 细胞群中富集。使用针对间充质和上皮细胞表面分子和荧光的抗体,我们可以轻松区分成牙本质细胞和成釉细胞,并分离每个细胞进行进一步研究。这些小鼠将作为牙齿发育和再生的有用模型,并为体内和体外成牙本质细胞和成釉细胞的分化过程提供同时观察。