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Notch 通过调节核纤层蛋白 A 来协调牙周韧带的成熟。

Notch Coordinates Periodontal Ligament Maturation through Regulating Lamin A.

机构信息

Department of Orthodontics, University Clinic of Dental Medicine, University of Geneva, Geneva, Switzerland.

Stem Cells & Regenerative Medicine Laboratory, Peninsula Dental School, Faculty of Medicine and Dentistry, University of Plymouth, Plymouth, UK.

出版信息

J Dent Res. 2019 Nov;98(12):1357-1366. doi: 10.1177/0022034519871448. Epub 2019 Aug 28.

Abstract

Tooth eruption is a continuous biological process with dynamic changes at cellular and tissue levels, particularly within the periodontal ligament (PDL). Occlusion completion is a significant physiological landmark of dentition establishment. However, the importance of the involvement of molecular networks engaging in occlusion establishment on the final PDL maturation is still largely unknown. In this study, using rat and mouse molar teeth and a human PDL cell line for RNAseq and proteomic analysis, we systematically screened the key molecular links in regulating PDL maturation before and after occlusion establishment. We discovered Notch, a key molecular pathway in regulating stem cell fate and differentiation, is a major player in the event. Intercepting the Notch pathway by deleting its key canonical transcriptional factor, , using a conditional knockout strategy in the mice delayed PDL maturation. We also identified that Lamin A, a cell nuclear lamina member, is a unique marker of PDL maturation, and its expression is under the control of Notch signaling. Our study therefore provides a deep insight of how PDL maturation is regulated at the molecular level, and we expect the outcomes to be applied for a better understanding of the molecular regulation networks in physiological conditions such as tooth eruption and movement and also for periodontal diseases.

摘要

牙齿萌出是一个持续的生物学过程,在细胞和组织水平上都有动态变化,特别是在牙周韧带(PDL)中。咬合完成是牙列建立的一个重要生理标志。然而,参与咬合建立的分子网络在最终 PDL 成熟中的作用在很大程度上仍然未知。在这项研究中,我们使用大鼠和小鼠磨牙以及人牙周膜细胞系进行 RNAseq 和蛋白质组学分析,系统筛选了在咬合建立前后调节 PDL 成熟的关键分子联系。我们发现 Notch 是调节干细胞命运和分化的关键分子途径,是该事件的主要参与者。通过在小鼠中使用条件性敲除策略删除其关键的经典转录因子,截获 Notch 途径会延迟 PDL 成熟。我们还发现,核纤层蛋白 A,一种细胞核层成员,是 PDL 成熟的独特标志物,其表达受 Notch 信号的控制。因此,我们的研究深入了解了 PDL 成熟在分子水平上是如何受到调节的,我们期望这些结果能够更好地理解牙齿萌出和移动等生理条件下的分子调节网络,以及牙周病的分子调节网络。

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