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首页> 外文期刊>Journal of cellular physiology. >Transcriptional regulation of the basic helix-loop-helix factor AmeloD during tooth development
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Transcriptional regulation of the basic helix-loop-helix factor AmeloD during tooth development

机译:基本的转录调控在牙齿AmeloD helix-loop-helix因素发展

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摘要

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 amelo-blasts. 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.
机译:epithelial-mesenchymal交互基本的起始和监管牙齿的发展。牙齿发育开始,大量的增长因素是由口腔上皮细胞分泌的间质细胞中扮演关键的角色分化。口腔上皮干细胞分化成一些细胞类型,包括内在的搪瓷上皮细胞,然后分化成搪瓷matrix-secreting amelo-blasts。我们报道了这部小说basic-helix-loop-helixAmeloD,转录因子是积极参与在牙齿的监管机构的发展口腔上皮细胞的能动性。AmeloD仍的基因调控机制未知的。机制在调节AmeloD表达式牙齿发育。重要的早期阶段的牙齿形成,我们发现TGF -β1诱导AmeloD表达式和造釉细胞分化口腔上皮细胞系,SF2。磷酸化ERK1/2 Smad2/3诱导AmeloD表达式,而使用MEK进行治疗抑制剂U0126,抑制AmeloD归纳。启动子分析AmeloD透露的近端启动子AmeloD显示高的活动在口腔上皮细胞系,增强后TGF -β1的刺激。结果表明,TGF -β1激活AmeloD通过ERK1/2磷酸化转录。发现的机制提供新的视角控制牙齿发育。

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