Ge Yaneng, Kong Ziren, Guo Yongwen, Tang Wei, Guo Weihua, Tian Weidong
State Key Laboratory of Oral Diseases, Sichuan University, Chengdu, PR China; Department of Oral and Maxillofacial Surgery, West China College of Stomatology, Sichuan University, Chengdu, PR China.
State Key Laboratory of Oral Diseases, Sichuan University, Chengdu, PR China; Department of Orthodontics, West China College of Stomatology, Sichuan University, Chengdu, PR China.
Arch Oral Biol. 2013 Feb;58(2):151-9. doi: 10.1016/j.archoralbio.2012.04.017. Epub 2012 May 18.
The rodent incisor cervical loop and molar Hertwig's epithelial root sheath (HERS) are common models used for investigating tooth root generation. The purpose of the present study was to gain a better understanding of the molecular mechanisms mediating root development by determining the distinctive gene and protein expression profiles of each during different stages of development.
In this study, we used quantitative real time reverse transcription-PCR and immunohistochemistry to analyse the expression levels of high mobility group AT-hook 2, ameloblastin, amelogenin, dentine sialoprotein, dentine matrix protein 1, osteocalcin, and bone sialoprotein in rat epithelial and mesenchymal cells isolated at postnatal days 4 and 8.
Results showed that the expression of these genes and proteins was up-regulated in cervical loop epithelial cells, but decreased or unchanged in other cells during development. This increase in expression in the incisor cervical loop may be due to the interaction of the inner incisor dental papilla cells, which are the niche cells of cervical loop epithelial cells and demonstrated up-regulated expression of the corresponding proteins, revealing a complex and dynamic interplay of these molecules during neonatal tooth development.
These findings provide novel insights into the molecular processes underlying crown development of rodent incisors, and contribute to our overall understanding of the pathogenic processes of tooth root dysontogenesis.
啮齿动物切牙颈环和磨牙赫特维希上皮根鞘(HERS)是用于研究牙根形成的常用模型。本研究的目的是通过确定每个模型在不同发育阶段独特的基因和蛋白质表达谱,更好地了解介导牙根发育的分子机制。
在本研究中,我们使用定量实时逆转录PCR和免疫组织化学方法,分析出生后第4天和第8天分离的大鼠上皮细胞和间充质细胞中高迁移率族AT钩蛋白2、成釉蛋白、釉原蛋白、牙本质涎蛋白、牙本质基质蛋白1、骨钙素和骨涎蛋白的表达水平。
结果显示,在发育过程中,这些基因和蛋白质的表达在颈环上皮细胞中上调,但在其他细胞中降低或不变。切牙颈环中表达的增加可能是由于切牙内牙乳头细胞的相互作用,切牙内牙乳头细胞是颈环上皮细胞的龛细胞,其相应蛋白质的表达上调,揭示了这些分子在新生牙发育过程中复杂而动态的相互作用。
这些发现为啮齿动物切牙冠部发育的分子过程提供了新的见解,并有助于我们对牙根发育异常致病过程的全面理解。