Regulatory role of N-myc downregulated genes in amelogenesis in rats

IF 2.9 4区 生物学 Q3 CELL BIOLOGY
Dong-Wook Yang, Jee-Hae Kang, Min-Seok Kim, Sun-Hun Kim
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Abstract

Cytodifferentiation of odontogenic cells, a late stage event in odontogenesis is based on gene regulation. However, studies on the identification of the involved genes are scarce. The present study aimed to search for molecules for the cytodifferentiation of ameloblastic cells in rats. Differential display-PCR revealed a differentially expressed gene between cap/early bell stage and hard tissue formation stage in molars. This gene was identified as N-myc Downregulated Gene 1 (Ndrg1), which is the first report in tooth development. Real time PCR and western blotting confirmed that the mRNA level of Ndrg1 was higher during enamel formation than the cap stage. Ndrg1 expression was upregulated in the early bell, crown, and root stages in a time-dependent manner. These patterns of expression were similar in Ndrg2, but Ndrg3 and Ndrg4 levels did not change during the developmental stages. Immunofluorescence revealed that strong immunoreactivity against Ndrg1 were detected in differentiated ameloblasts only, not inner enamel epithelium, odontoblasts and ameloblastic cells in defected enamel regions. Alkaline phosphatase and alizarin red s stains along with real time PCR, revealed that Ndrg1 and Ndrg2 were involved in cytodifferentiation and enamel matrix mineralization by selectively regulating amelogenin and ameloblastin genes in SF2 ameloblastic cells. These results suggest that Ndrg may play a crucial functional role in the cytodifferentiation of ameloblasts for amelogenesis.

Abstract Image

N-myc下调基因在大鼠骨髓形成中的调控作用
牙本质细胞的细胞分化是牙本质发生过程中的一个晚期阶段,是以基因调控为基础的。然而,有关相关基因的研究却很少。本研究旨在寻找大鼠成釉细胞细胞分化的分子。差异显示-PCR 发现,在磨牙的帽状/早期钟状阶段和硬组织形成阶段,有一种基因表达不同。该基因被鉴定为N-myc下调基因1(Ndrg1),这是首次关于牙齿发育的报道。实时 PCR 和 Western 印迹证实,Ndrg1 的 mRNA 水平在釉质形成期高于冠形成期。Ndrg1的表达在早期钟、牙冠和牙根阶段以时间依赖的方式上调。这些表达模式与 Ndrg2 相似,但 Ndrg3 和 Ndrg4 的水平在各发育阶段没有变化。免疫荧光显示,仅在分化的成釉细胞中检测到针对 Ndrg1 的强免疫反应,而在釉质缺损区域的内釉上皮、牙本质母细胞和成釉细胞中未检测到。碱性磷酸酶和茜素红染色以及实时 PCR 发现,Ndrg1 和 Ndrg2 通过选择性调节 SF2 成釉细胞中的釉质原蛋白和成釉细胞蛋白基因,参与细胞分化和釉质基质矿化。这些结果表明,Ndrg可能在釉母细胞的细胞分化过程中对釉质形成起着至关重要的作用。
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来源期刊
Journal of Molecular Histology
Journal of Molecular Histology 生物-细胞生物学
CiteScore
5.90
自引率
0.00%
发文量
68
审稿时长
1 months
期刊介绍: The Journal of Molecular Histology publishes results of original research on the localization and expression of molecules in animal cells, tissues and organs. Coverage includes studies describing novel cellular or ultrastructural distributions of molecules which provide insight into biochemical or physiological function, development, histologic structure and disease processes. Major research themes of particular interest include: - Cell-Cell and Cell-Matrix Interactions; - Connective Tissues; - Development and Disease; - Neuroscience. Please note that the Journal of Molecular Histology does not consider manuscripts dealing with the application of immunological or other probes on non-standard laboratory animal models unless the results are clearly of significant and general biological importance. The Journal of Molecular Histology publishes full-length original research papers, review articles, short communications and letters to the editors. All manuscripts are typically reviewed by two independent referees. The Journal of Molecular Histology is a continuation of The Histochemical Journal.
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