Yamashiro Takashi, Zheng Li, Shitaku Yuko, Saito Masahiro, Tsubakimoto Takanori, Takada Kenji, Takano-Yamamoto Teruko, Thesleff Irma
Department of Orthodontics and Dentofacial Orthopedics, Graduate School of Dentistry, Osaka University, 1-8 Yamadaoka, Suita Osaka 565-0871, Japan.
Differentiation. 2007 Jun;75(5):452-62. doi: 10.1111/j.1432-0436.2006.00150.x. Epub 2007 Feb 5.
We have explored the role of Wnt signaling in dentinogenesis of mouse molar teeth. We found that Wnt10a was specifically associated with the differentiation of odontoblasts and that it showed striking colocalization with dentin sialophosphoprotein (Dspp) expression in secretory odontoblasts. Dspp is a tooth specific non-collagenous matrix protein and regulates dentin mineralization. Transient overexpression of Wnt10 in C3H10T1/2, a pluripotent fibroblast cell line induced Dspp mRNA. Interestingly, this induction occurred only when transfected cells were cultured on Matrigel basement membrane extracts. These findings indicated that Wnt10a is an upstream regulatory molecule for Dspp expression, and that cell-matrix interaction is essential for induction of Dspp expression. Furthermore, Wnt10a was specifically expressed in the epithelial signaling centers regulating tooth development, the primary and secondary enamel knots. The spatial and temporal distribution of Wnt10a mRNA demonstrated that the expression shifts from the secondary enamel knots, to the underlying preodontoblasts in the tips of future cusps. The expression patterns and overexpression studies together indicate that Wnt10a is a key molecule for dentinogenesis and that it is associated with the cell-matrix interactions regulating odontoblast differentiation. We conclude that Wnt10a may link the differentiation of odontoblasts and cusp morphogenesis.
我们探究了Wnt信号通路在小鼠磨牙牙本质形成中的作用。我们发现Wnt10a与成牙本质细胞的分化特别相关,并且在分泌期成牙本质细胞中它与牙本质涎磷蛋白(Dspp)的表达呈现出显著的共定位。Dspp是一种牙齿特异性非胶原蛋白基质蛋白,可调节牙本质矿化。在多能成纤维细胞系C3H10T1/2中瞬时过表达Wnt10可诱导Dspp mRNA表达。有趣的是,这种诱导仅在转染细胞在基质胶基底膜提取物上培养时才会发生。这些发现表明Wnt10a是Dspp表达的上游调节分子,并且细胞-基质相互作用对于Dspp表达的诱导至关重要。此外,Wnt10a在调节牙齿发育的上皮信号中心,即初级和次级釉结中特异性表达。Wnt10a mRNA的时空分布表明其表达从次级釉结转移至未来牙尖尖端下方的前成牙本质细胞。表达模式和过表达研究共同表明Wnt10a是牙本质形成的关键分子,并且它与调节成牙本质细胞分化的细胞-基质相互作用相关。我们得出结论,Wnt10a可能将成牙本质细胞的分化与牙尖形态发生联系起来。