Centre for Craniofacial and Regenerative Biology, Dental Institute, Kings College London, London, UK.
Sci Rep. 2017 Jun 8;7(1):3102. doi: 10.1038/s41598-017-03145-6.
In non-growing teeth, such as mouse and human molars, primary odontoblasts are long-lived post-mitotic cells that secrete dentine throughout the life of the tooth. New odontoblast-like cells are only produced in response to a damage or trauma. Little is known about the molecular events that initiate mesenchymal stem cells to proliferate and differentiate into odontoblast-like cells in response to dentine damage. The reparative and regenerative capacity of multiple mammalian tissues depends on the activation of Wnt/β-catenin signaling pathway. In this study, we investigated the molecular role of Wnt/β-catenin signaling pathway in reparative dentinogenesis using an in vivo mouse tooth damage model. We found that Axin2 is rapidly upregulated in response to tooth damage and that these Axin2-expressing cells differentiate into new odontoblast-like cells that secrete reparative dentine. In addition, the Axin2-expressing cells produce a source of Wnt that acts in an autocrine manner to modulate reparative dentinogenesis.
在非生长牙齿中,如老鼠和人类的磨牙,原代成牙本质细胞是具有长寿命的有丝分裂后细胞,它们在牙齿的整个生命周期中分泌牙本质。只有在受到损伤或创伤时,才会产生新的成牙本质细胞样细胞。目前对于引发间充质干细胞增殖并分化为成牙本质细胞样细胞以响应牙本质损伤的分子事件知之甚少。多种哺乳动物组织的修复和再生能力取决于 Wnt/β-catenin 信号通路的激活。在这项研究中,我们使用体内小鼠牙齿损伤模型研究了 Wnt/β-catenin 信号通路在修复性牙本质形成中的分子作用。我们发现 Axin2 对牙齿损伤迅速上调,并且这些表达 Axin2 的细胞分化为新的成牙本质细胞样细胞,分泌修复性牙本质。此外,表达 Axin2 的细胞产生 Wnt 的来源,以自分泌方式调节修复性牙本质形成。