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发育中小鼠门牙的基因表达与牙釉质结构

Gene expression and dental enamel structure in developing mouse incisor.

作者信息

Sehic Amer, Risnes Steinar, Khan Qalb-E-Saleem, Khuu Cuong, Osmundsen Harald

机构信息

Department of Oral Biology, University of Oslo, Box 1052 Blindern, 0316 Oslo, Norway.

出版信息

Eur J Oral Sci. 2010 Apr;118(2):118-30. doi: 10.1111/j.1600-0722.2010.00722.x.

Abstract

At the mouse incisor tip the initially differentiated ameloblasts produce a thin, prism-free enamel, while further apically, in the immediate adjacent segment, the enamel thickness increases and the four-layered enamel of mouse incisor is formed. Comparative gene-expression profiling was carried out on RNA isolated from these two segments of incisor tooth germs at embryonic day (E)17.5 and at postnatal days (P)0, 1, 2, and 10 using microarrays to measure messenger RNA (mRNA) and microRNA (miRNA) species present in the segments. Validation of expression data was achieved using real-time reverse transcription-polymerase chain reaction (RT-PCR) and western blotting. Bioinformatic data suggested enhanced cellular apoptosis in the incisal tip segment, which, together with diminished expression of the Amelx and Enam genes, may contribute to the production of the thin enamel seen in this tooth segment. For genes exhibiting higher levels of expression in the adjacent segment where complex enamel is being formed, bioinformatic analysis suggested significant associations with cellular functions involving the actin cytoskeleton, cellular development, morphology, and movement. This is suggested to reflect that ameloblasts with Tomes' process are being organized in transverse rows, facilitating the transverse movement that results in prism decussation in the inner enamel of the adjacent segment. Bioinformatic analysis of miRNA expression data lends support to these suggestions.

摘要

在小鼠切牙尖端,最初分化的成釉细胞产生一层薄的、无棱柱的釉质,而在更靠近根尖的紧邻节段,釉质厚度增加,小鼠切牙的四层釉质形成。在胚胎第17.5天以及出生后第0、1、2和10天,使用微阵列对从切牙牙胚的这两个节段分离的RNA进行了比较基因表达谱分析,以测量节段中存在的信使核糖核酸(mRNA)和微小核糖核酸(miRNA)种类。使用实时逆转录聚合酶链反应(RT-PCR)和蛋白质印迹法对表达数据进行了验证。生物信息学数据表明切牙尖端节段的细胞凋亡增强,这与Amelx和Enam基因表达的减少一起,可能导致了该牙段中薄釉质的产生。对于在正在形成复杂釉质的相邻节段中表达水平较高的基因,生物信息学分析表明它们与涉及肌动蛋白细胞骨架、细胞发育、形态和运动的细胞功能有显著关联。这表明具有托姆斯突的成釉细胞正在横向排列,促进了横向运动,从而导致相邻节段内釉质中棱柱交叉。对miRNA表达数据的生物信息学分析支持了这些观点。

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