Department of Oral Health and Development Sciences, Division of Pediatric Dentistry, Tohoku University Graduate School of Dentistry, Sendai, Japan.
Section of Oral Medicine for Children, Division of Oral Health, Growth and Development, Faculty of Dental Science, Kyushu University, Fukuoka, Japan.
J Cell Physiol. 2021 Nov;236(11):7533-7543. doi: 10.1002/jcp.30389. Epub 2021 Apr 12.
The epithelial-mesenchymal interactions are essential for the initiation and regulation of the development of teeth. Following the initiation of tooth development, numerous growth factors are secreted by the dental epithelium and mesenchyme that play critical roles in cellular differentiation. During tooth morphogenesis, the dental epithelial stem cells differentiate into several cell types, including inner enamel epithelial cells, which then differentiate into enamel matrix-secreting ameloblasts. Recently, we reported that the novel basic-helix-loop-helix transcription factor, AmeloD, is actively engaged in the development of teeth as a regulator of dental epithelial cell motility. However, the gene regulation mechanism of AmeloD is still unknown. In this study, we aimed to uncover the mechanisms regulating AmeloD expression during tooth development. By screening growth factors that are important in the early stages of tooth formation, we found that TGF-β1 induced AmeloD expression and ameloblast differentiation in the dental epithelial cell line, SF2. TGF-β1 phosphorylated ERK1/2 and Smad2/3 to induce AmeloD expression, whereas treatment with the MEK inhibitor, U0126, inhibited AmeloD induction. Promoter analysis of AmeloD revealed that the proximal promoter of AmeloD showed high activity in dental epithelial cell lines, which was enhanced following TGF-β1 stimulation. These results suggested that TGF-β1 activates AmeloD transcription via ERK1/2 phosphorylation. Our findings provide new insights into the mechanisms that govern tooth development.
上皮-间充质相互作用对于牙齿的发生和发育的调节至关重要。在牙齿发育的起始之后,许多生长因子由牙上皮和间充质分泌,这些生长因子在细胞分化中发挥关键作用。在牙齿形态发生过程中,牙上皮干细胞分化为几种细胞类型,包括内釉上皮细胞,然后分化为分泌釉基质的成釉细胞。最近,我们报道了新型碱性螺旋-环-螺旋转录因子 AmeloD 作为牙上皮细胞迁移的调节剂积极参与牙齿的发育。然而,AmeloD 的基因调控机制尚不清楚。在这项研究中,我们旨在揭示调节牙齿发育过程中 AmeloD 表达的机制。通过筛选在牙齿形成早期阶段重要的生长因子,我们发现 TGF-β1 诱导牙上皮细胞系 SF2 中的 AmeloD 表达和成釉细胞分化。TGF-β1 磷酸化 ERK1/2 和 Smad2/3 诱导 AmeloD 表达,而 MEK 抑制剂 U0126 的处理则抑制 AmeloD 诱导。AmeloD 的启动子分析表明,AmeloD 的近端启动子在牙上皮细胞系中具有高活性,并且在 TGF-β1 刺激后增强。这些结果表明 TGF-β1 通过 ERK1/2 磷酸化激活 AmeloD 转录。我们的发现为调控牙齿发育的机制提供了新的见解。