牙骨质
轴2
细胞生物学
化学
间充质干细胞
间充质
钥匙(锁)
生物
病理
生物化学
Wnt信号通路
医学
信号转导
牙本质
生态学
作者
Xudong Xie,Jun Wang,Ke Wang,C. Li,S Zhang,Dian Jing,Chunmei Xu,Xiaofang Wang,Hu Zhao,Jian Q. Feng
标识
DOI:10.1177/0022034519871021
摘要
To date, attempts to regenerate functional periodontal tissues (including cementum) are largely unsuccessful due to a lack of full understanding about the cellular origin (epithelial or mesenchymal cells) essential for root cementum growth. To address this issue, we first identified a rapid cementum growth window from the ages of postnatal day 28 (P28) to P56. Next, we showed that expression patterns of Axin2 and β-catenin within cementum-forming periodontal ligament (PDL) cells are negatively associated with rapid cementum growth. Furthermore, cell lineage tracing studies revealed that the Axin2 + -mesenchymal PDL cells and their progeny rapidly expand and directly contribute to postnatal acellular and cellular cementum growth. In contrast, the number of K14 + epithelial cells, which were initially active at early stages of development, was reduced during rapid cementum formation from P28 to P56. The in vivo cell ablation of these Axin2 + cells using Axin2 CreERT2/+ ; R26R DTA/+ mice led to severe cementum hypoplasia, whereas constitutive activation of β-catenin in the Axin2 + cells resulted in an acceleration in cellular cementogenesis plus a transition from acellular cementum to cellular cementum. Thus, we conclude that Axin2 + -mesenchymal PDL cells, instead of K14 + epithelial cells, significantly contribute to rapid cementum growth.
科研通智能强力驱动
Strongly Powered by AbleSci AI