DMP1型
延伸率
成牙本质细胞
Wnt信号通路
内斯汀
牙本质
连环蛋白
鱼腥草素骨
细胞生物学
化学
连环素
臼齿
内胚层
生物
分子生物学
男科
信号转导
生物化学
牙科
干细胞
医学
基因
材料科学
骨钙素
病毒基质蛋白
古生物学
碱性磷酸酶
神经干细胞
酶
冶金
极限抗拉强度
作者
Jun Wang,Yong Jiang,Xudong Xie,Shiwen Zhang,Chunmei Xu,Yinghong Zhou,Jian Q. Feng
出处
期刊:Oral Diseases
[Wiley]
日期:2020-12-12
卷期号:28 (2): 442-451
被引量:8
摘要
In this study, we attempted to define the precise window of time for molar root elongation using a gain-of-function mutation of β-catenin model.Both the control and constitutively activated β-catenin (CA-β-cat) mice received a one-time tamoxifen administration (for activation of β-catenin at newborn, postnatal day 3, or 5, or 7, or 9) and were harvested at the same stage of P21. Multiple approaches were used to define the window of time of postnatal tooth root formation.In the early activation groups (tamoxifen induction at newborn, or P3 or P5), there was a lack of molar root elongation in the CA-β-cat mice. When induced at P7, the root length was slightly reduced at P21. However, the root length was essentially the same as that in the control when β-cat activated at P9. This study indicates that root elongation occurs in a narrow time of window, which is highly sensitive to a change of β-catenin levels. Molecular studies showed a drastic decrease in the levels of nuclear factor I-C (NFIC) and osterix (OSX), plus sharp reductions of odontoblast differentiation markers, including Nestin, dentin sialoprotein (DSP), and dentin matrix protein 1 (DMP1) at both mRNA and protein levels.Murine molar root elongation is precisely regulated by the Wnt/β-catenin signaling within a narrow window of time (newborn to day 5).
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