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Wnt/β-连环蛋白信号通路促进体外前成牙本质细胞的形成。

Wnt/β-Catenin Signaling Promotes the Formation of Preodontoblasts In Vitro.

机构信息

Department of Craniofacial Sciences, University of Connecticut Health Center, Farmington, CT, USA.

出版信息

J Dent Res. 2021 Apr;100(4):387-396. doi: 10.1177/0022034520967353. Epub 2020 Oct 26.

Abstract

Odontoblast differentiation is a complex and multistep process regulated by signaling pathways, including the Wnt/β-catenin signaling pathway. Both positive and negative effects of Wnt/β-catenin signaling on dentinogenesis have been reported, but the underlying mechanisms of these conflicting results are still unclear. To gain a better insight into the role of Wnt/β-catenin in dentinogenesis, we used dental pulp cells from a panel of transgenic mice, in which fluorescent protein expression identifies cells at different stages of odontoblast and osteoblast differentiation. Our results showed that exposure of pulp cells to WNT3a at various times and durations did not induce premature differentiation of odontoblasts. These treatments supported the survival of undifferentiated cells in dental pulp and promoted the formation of 2.3GFP preodontoblasts and their rapid transition into differentiated odontoblasts expressing DMP1-Cherry and DSPP-Cerulean transgenes. WNT3a also promoted osteogenesis in dental pulp cultures. These findings provide critical information for the development of improved treatments for vital pulp therapy and dentin regeneration.

摘要

成牙本质细胞分化是一个复杂的多步骤过程,受信号通路调控,包括 Wnt/β-catenin 信号通路。已经报道了 Wnt/β-catenin 信号对牙本质生成的正反两方面的影响,但这些相互矛盾结果的潜在机制仍不清楚。为了更好地了解 Wnt/β-catenin 在牙本质生成中的作用,我们使用了一组转基因小鼠的牙髓细胞,其中荧光蛋白的表达可识别处于成牙本质细胞和成骨细胞分化不同阶段的细胞。我们的结果表明,WNT3a 在不同时间和持续时间暴露于牙髓细胞不会诱导成牙本质细胞的过早分化。这些处理支持未分化细胞在牙髓中的存活,并促进 2.3GFP 前成牙本质细胞的形成及其快速过渡为表达 DMP1-Cherry 和 DSPP-Cerulean 转基因的分化成牙本质细胞。WNT3a 还促进了牙髓培养中的成骨作用。这些发现为开发用于活髓治疗和牙本质再生的改进治疗方法提供了重要信息。

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