Department of Pathology, School of Medicine, University of Alabama at Birmingham, Birmingham, AL, USA.
State Key Laboratory of Oral Diseases & National Center for Stomatology & National Clinical Research Center for Oral Diseases & Department of Orthodontics, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Int J Oral Sci. 2023 Aug 21;15(1):35. doi: 10.1038/s41368-023-00235-2.
The biomolecular mechanisms that regulate tooth root development and odontoblast differentiation are poorly understood. We found that Atp6i deficient mice (Atp6i) arrested tooth root formation, indicated by truncated Hertwig's epithelial root sheath (HERS) progression. Furthermore, Atp6i deficiency significantly reduced the proliferation and differentiation of radicular odontogenic cells responsible for root formation. Atp6i mice had largely decreased expression of odontoblast differentiation marker gene expression profiles (Col1a1, Nfic, Dspp, and Osx) in the alveolar bone. Atp6i mice sample RNA-seq analysis results showed decreased expression levels of odontoblast markers. Additionally, there was a significant reduction in Smad2/3 activation, inhibiting transforming growth factor-β (TGF-β) signaling in Atp6i odontoblasts. Through treating pulp precursor cells with Atp6i or wild-type OC bone resorption-conditioned medium, we found the latter medium to promote odontoblast differentiation, as shown by increased odontoblast differentiation marker genes expression (Nfic, Dspp, Osx, and Runx2). This increased expression was significantly blocked by anti-TGF-β1 antibody neutralization, whereas odontoblast differentiation and Smad2/3 activation were significantly attenuated by Atp6i OC conditioned medium. Importantly, ectopic TGF-β1 partially rescued root development and root dentin deposition of Atp6i mice tooth germs were transplanted under mouse kidney capsules. Collectively, our novel data shows that the prevention of TGF-β1 release from the alveolar bone matrix due to OC dysfunction may lead to osteopetrosis-associated root formation via impaired radicular odontoblast differentiation. As such, this study uncovers TGF-β1 /Smad2/3 as a key signaling pathway regulating odontoblast differentiation and tooth root formation and may contribute to future therapeutic approaches to tooth root regeneration.
调控牙根发育和成牙本质细胞分化的生物分子机制尚未完全阐明。我们发现,Atp6i 缺陷型小鼠(Atp6i)的牙根形成被阻断,表现为 Hertwig 上皮根鞘(HERS)的进展缩短。此外,Atp6i 缺陷显著降低了负责牙根形成的根状牙源性细胞的增殖和分化。Atp6i 小鼠牙槽骨中牙本质细胞分化标志物的基因表达谱(Col1a1、Nfic、Dspp 和 Osx)的表达显著减少。Atp6i 小鼠样本的 RNA-seq 分析结果显示,牙本质细胞标志物的表达水平降低。此外,Smad2/3 激活受到抑制,TGF-β(TGF-β)信号通路在 Atp6i 成牙本质细胞中被抑制。通过用 Atp6i 或野生型 OC 破骨细胞条件培养基处理牙髓前体细胞,我们发现后者培养基促进成牙本质细胞分化,表现为牙本质细胞分化标志物基因表达增加(Nfic、Dspp、Osx 和 Runx2)。抗 TGF-β1 抗体中和阻断了这种增加的表达,而 Atp6i OC 条件培养基显著减弱了成牙本质细胞分化和 Smad2/3 激活。重要的是,异位 TGF-β1 部分挽救了 Atp6i 小鼠牙胚的牙根发育和根状牙本质沉积,这些牙胚被移植到小鼠肾囊下。总之,我们的新数据表明,由于 OC 功能障碍导致 TGF-β1 从牙槽骨基质中释放受阻,可能通过损害根状成牙本质细胞分化导致与骨硬化症相关的牙根形成。因此,这项研究揭示了 TGF-β1/Smad2/3 作为调节成牙本质细胞分化和牙根形成的关键信号通路,并可能为未来的牙根再生治疗方法做出贡献。