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与兔子牙齿替换相关的基因表达模式,一种用于研究哺乳动物牙齿替换机制的新模型。

Gene expression patterns associated with dental replacement in the rabbit, a new model for the mammalian dental replacement mechanisms.

作者信息

Bertonnier-Brouty Ludivine, Viriot Laurent, Joly Thierry, Charles Cyril

机构信息

Institut de Génomique Fonctionnelle de Lyon, Université de Lyon, CNRS UMR 5242, Ecole Normale Supérieure de Lyon, Université Claude Bernard Lyon 1, Lyon, France.

Laboratoire de Biologie tissulaire et Ingénierie thérapeutique, Université de Lyon, CNRS UMR5305, Université Claude Bernard Lyon 1, Lyon, France.

出版信息

Dev Dyn. 2021 Oct;250(10):1494-1504. doi: 10.1002/dvdy.335. Epub 2021 Mar 30.

Abstract

BACKGROUND

Unlike many vertebrates with continuous dental replacement, mammals have a maximum of two dental generations. Due to the absence of dental replacement in the laboratory mouse, the mechanisms of the mammalian tooth replacement system are poorly known. In this study, we use the European rabbit as a model for mammalian tooth development and replacement.

RESULTS

We provide data on some key regulators of tooth development. We detected the presence of SOX2 in both the replacement dental lamina and the rudimentary successional dental lamina of unreplaced molars, indicating that SOX2 may not be sufficient to initiate and maintain tooth replacement. We showed that Shh does not seem to be directly involved in tooth replacement. The transient presence of the rudimentary successional dental lamina in the molar allowed us to identify genes that could be essential for the initiation or the maintenance of tooth replacement. Hence, the locations of Sostdc1, RUNX2, and LEF1 vary between the deciduous premolar, the replacement premolar, and the molar, indicating possible roles in tooth replacement.

CONCLUSION

According to our observations, initiation and the maintenance of tooth replacement correlate with the presence of LEF1 cells and the absence of both mesenchymal RUNX2 and epithelial Sostdc1 cells.

摘要

背景

与许多具有连续牙齿替换的脊椎动物不同,哺乳动物最多有两代牙齿。由于实验室小鼠不存在牙齿替换,哺乳动物牙齿替换系统的机制鲜为人知。在本研究中,我们使用欧洲兔作为哺乳动物牙齿发育和替换的模型。

结果

我们提供了一些牙齿发育关键调节因子的数据。我们在替换牙板和未替换磨牙的原始继承牙板中均检测到SOX2的存在,这表明SOX2可能不足以启动和维持牙齿替换。我们发现Shh似乎不直接参与牙齿替换。磨牙中原始继承牙板的短暂存在使我们能够鉴定出对牙齿替换的启动或维持可能至关重要的基因。因此,Sostdc1、RUNX2和LEF1在乳前磨牙、替换前磨牙和磨牙中的位置有所不同,表明它们在牙齿替换中可能发挥作用。

结论

根据我们的观察,牙齿替换的启动和维持与LEF1细胞的存在以及间充质RUNX2和上皮Sostdc1细胞的缺失相关。

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