首页> 外文期刊>Journal of Endodontics: Official Journal of American Association of Endodontists >Lymphoid enhancer-binding factor 1 expression precedes dentin sialophosphoprotein expression during rat odontoblast differentiation and regeneration
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Lymphoid enhancer-binding factor 1 expression precedes dentin sialophosphoprotein expression during rat odontoblast differentiation and regeneration

机译:大鼠成牙本质细胞分化和再生过程中,淋巴增强剂结合因子1的表达先于牙本质唾液磷蛋白的表达

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Introduction: The molecular mechanisms behind odontoblast differentiation remain obscure. Lymphoid enhancer-binding factor 1 (Lef1) is a transcription factor that mediates Wnt signaling and has been suggested to regulate dentin sialophosphoprotein (Dspp) expression in vitro. This study aimed to clarify their precise relationship in the process of odontoblast differentiation in vivo. Methods: The detailed spatiotemporal expression patterns of Lef1 and Dspp together with other known and putative odontoblast differentiation markers such as P21 and heat-shock protein 25 (Hsp25) were examined by in situ hybridization and immunohistochemistry on paraffin sections of rat incisors and developing molars at postnatal days 1-100. To observe odontoblast regeneration following tooth injury, a cavity was prepared on the upper first molar of 10-week-old rats and the expressions of Lef1 and Dspp were investigated. Results: Following undifferentiated state expressing none of these examined markers, preodontoblasts begun to express P21, Lef1 and Hsp25 according to their progress of differentiation, although Dspp was undetectable. Immature odontoblasts commenced transcribing Dspp simultaneously with dentin calcification. Lef1, Dspp and Hsp25 were co-expressed in mature odontoblasts. In contrast to continuously growing incisors, Lef1, Dspp and P21 were down-regulated in the resting odontoblasts in molars when primary dentin formation was completed. Remarkably, Lef1 expression also preceded Dspp expression in newly differentiated odontoblast-like cells during the pulpal healing process after tooth injury. Conclusions: Lef1 expression precedes Dspp expression without exception in both primary and reparative dentinogeneses. Our results suggest that Lef1 might play a key role in odontoblast differentiation through regulating Dspp expression.
机译:简介:成牙本质细胞分化的分子机制仍然不清楚。淋巴增强因子结合因子1(Lef1)是介导Wnt信号的转录因子,已被建议在体外调节牙本质唾液磷蛋白(Dspp)的表达。这项研究旨在阐明它们在成牙本质细胞体内分化过程中的确切关系。方法:通过原位杂交和免疫组织化学方法,在大鼠门牙石蜡切片和正畸磨牙上,通过分子杂交和免疫组化检查Lef1和Dspp以及其他已知的和公认的成牙本质细胞分化标志物如P21和热休克蛋白25(Hsp25)的时空表达模式。产后1-100天。为了观察牙齿损伤后成牙本质细胞的再生,在10周龄大鼠的第一磨牙上准备了一个腔,并研究了Lef1和Dspp的表达。结果:在未分化状态下不表达这些被检测标记物后,成牙本质细胞根据其分化进程开始表达P21,Lef1和Hsp25,尽管无法检测到Dspp。不成熟的成牙本质细胞开始与牙本质钙化同时转录Dspp。 Lef1,Dspp和Hsp25在成熟成牙本质细胞中共表达。与持续增长的门牙形成对照的是,当初级牙本质形成完成时,在静息的成牙本质成牙本质细胞中Lef1,Dspp和P21被下调。值得注意的是,在牙齿损伤后的牙髓愈合过程中,新分化的成牙本质细胞样细胞中,Lef1表达也先于Dspp表达。结论:在初级和修复性牙本质病中,Lef1表达先于Dspp表达。我们的结果表明,Lef1可能通过调节Dspp表达在成牙本质细胞分化中起关键作用。

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