FGF signaling modulates mechanotransduction/WNT signaling in progenitors during tooth root development.

IF 14.3 1区 医学 Q1 CELL & TISSUE ENGINEERING
Fei Pei, Tingwei Guo, Mingyi Zhang, Li Ma, Junjun Jing, Jifan Feng, Thach-Vu Ho, Quan Wen, Yang Chai
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Abstract

Stem/progenitor cells differentiate into different cell lineages during organ development and morphogenesis. Signaling pathway networks and mechanotransduction are important factors to guide the lineage commitment of stem/progenitor cells during craniofacial tissue morphogenesis. Here, we used tooth root development as a model to explore the roles of FGF signaling and mechanotransduction as well as their interaction in regulating the progenitor cell fate decision. We show that Fgfr1 is expressed in the mesenchymal progenitor cells and their progeny during tooth root development. Loss of Fgfr1 in Gli1+ progenitors leads to hyperproliferation and differentiation, which causes narrowed periodontal ligament (PDL) space with abnormal cementum/bone formation leading to ankylosis. We further show that aberrant activation of WNT signaling and mechanosensitive channel Piezo2 occurs after loss of FGF signaling in Gli1-CreER;Fgfr1fl/fl mice. Overexpression of Piezo2 leads to increased osteoblastic differentiation and decreased Piezo2 leads to downregulation of WNT signaling. Mechanistically, an FGF/PIEZO2/WNT signaling cascade plays a crucial role in modulating the fate of progenitors during root morphogenesis. Downregulation of WNT signaling rescues tooth ankylosis in Fgfr1 mutant mice. Collectively, our findings uncover the mechanism by which FGF signaling regulates the fate decisions of stem/progenitor cells, and the interactions among signaling pathways and mechanotransduction during tooth root development, providing insights for future tooth root regeneration.

Abstract Image

牙根发育过程中,FGF 信号调节祖细胞中的机械传导/WNT 信号。
干细胞/祖细胞在器官发育和形态发生过程中会分化成不同的细胞系。信号通路网络和机械传导是颅面组织形态发生过程中引导干细胞/祖细胞系承的重要因素。在这里,我们以牙根的发育为模型,探讨了FGF信号传导和机械传导在调控祖细胞命运决定中的作用及其相互作用。我们发现,在牙根发育过程中,Fgfr1在间充质祖细胞及其后代中表达。Gli1+ 祖细胞中 Fgfr1 的缺失会导致过度增殖和分化,从而造成牙周韧带(PDL)空间狭窄,骨水泥/骨形成异常,导致强直。我们进一步发现,Gli1-CreER;Fgfr1fl/fl 小鼠失去 FGF 信号后,WNT 信号和机械敏感通道 Piezo2 会发生异常激活。过表达 Piezo2 会导致成骨细胞分化增加,而减少 Piezo2 会导致 WNT 信号下调。从机制上讲,FGF/PIEZO2/WNT 信号级联在根形态发生过程中对祖细胞的命运起着至关重要的调节作用。下调 WNT 信号可挽救 Fgfr1 突变小鼠的牙齿强直。总之,我们的研究结果揭示了牙根发育过程中FGF信号调节干细胞/祖细胞命运决定的机制,以及信号通路和机械传导之间的相互作用,为未来的牙根再生提供了启示。
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来源期刊
Bone Research
Bone Research CELL & TISSUE ENGINEERING-
CiteScore
20.00
自引率
4.70%
发文量
289
审稿时长
20 weeks
期刊介绍: Established in 2013, Bone Research is a newly-founded English-language periodical that centers on the basic and clinical facets of bone biology, pathophysiology, and regeneration. It is dedicated to championing key findings emerging from both basic investigations and clinical research concerning bone-related topics. The journal's objective is to globally disseminate research in bone-related physiology, pathology, diseases, and treatment, contributing to the advancement of knowledge in this field.
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