Ono Y, Kaku M, Thant L, Iwama H, Arai M, Mizukoshi M, Dobashi A, Kitami M, Taketo M M, Ohazama A, Saito I, Uoshima K
Division of Bio-Prosthodontics, Faculty of Dentistry & Graduate School of Medical and Dental Sciences, Niigata University, Niigata, Japan.
Division of Orthodontics, Faculty of Dentistry & Graduate School of Medical and Dental Sciences, Niigata University, Niigata, Japan.
J Dent Res. 2025 Feb;104(2):183-192. doi: 10.1177/00220345241286490. Epub 2024 Nov 25.
Regeneration of periodontal tissue, particularly the cementum-periodontal ligament (PDL)-bone complex, has long been challenging because the differentiation kinetics of cells and the molecular pathways contributing to the regeneration process are largely unknown. We aimed to evaluate the cell behavior and molecular pathways that contribute to periodontal tissue regeneration in vivo. We analyzed the process of periodontal tissue regeneration through subrenal capsule transplantation of immediately extracted molars in mice. We showed that the regenerated periodontal tissue in the subrenal capsule was morphologically comparable to the intact periodontal tissue, with increased cellular cementum thickness in the apical region. Cell tracing analysis revealed that the cells comprising the regenerated periodontal tissue were derived from transplanted teeth and were indispensable for periodontal tissue regeneration, whereas recipient mouse-derived cells partly contributed to angiogenesis. Bioinformatics analysis based on the gene expression profile in the transplanted teeth indicated that Wnt/β-catenin signaling is involved in periodontal tissue regeneration, which was further confirmed through β-catenin immunohistochemistry. Moreover, the constitutive activation of β-catenin in the cells of transplanted teeth was found to promote accelerated cellular cementum apposition, while the conditional knockout of β-catenin in the cells of transplanted teeth suppressed cellular cementum apposition. Notably, the manipulation of Wnt/β-catenin signaling did not interfere with the bone-PDL-cementum complex, while endogenous osteoclast activity was affected in bone. Our results demonstrated the essential roles of endogenous PDL cells in periodontal tissue regeneration and that Wnt/β-catenin signaling is involved in this process, particularly cellular cementum apposition. Hence, controlling this pathway could promote cementum regeneration, which is a critical process for the regeneration of the cementum-PDL-bone complex. This study provides novel insights into cell behavior and signaling pathways that will advance practical periodontal tissue regeneration.
长期以来,牙周组织的再生,尤其是牙骨质 - 牙周韧带(PDL) - 骨复合体的再生一直具有挑战性,因为细胞的分化动力学以及促成再生过程的分子途径在很大程度上尚不清楚。我们旨在评估体内促成牙周组织再生的细胞行为和分子途径。我们通过将立即拔除的磨牙移植到小鼠肾被膜下,分析了牙周组织再生的过程。我们发现肾被膜下再生的牙周组织在形态上与完整的牙周组织相当,根尖区域的细胞性牙骨质厚度增加。细胞追踪分析表明,构成再生牙周组织的细胞来源于移植牙,对牙周组织再生不可或缺,而受体小鼠来源的细胞部分促成了血管生成。基于移植牙基因表达谱的生物信息学分析表明,Wnt/β - 连环蛋白信号通路参与牙周组织再生,β - 连环蛋白免疫组织化学进一步证实了这一点。此外,发现移植牙细胞中β - 连环蛋白的组成性激活促进了细胞性牙骨质的加速附着,而移植牙细胞中β - 连环蛋白的条件性敲除则抑制了细胞性牙骨质的附着。值得注意的是,对Wnt/β - 连环蛋白信号通路的操控并未干扰骨 - PDL - 牙骨质复合体,而骨中的内源性破骨细胞活性受到了影响。我们的结果证明了内源性PDL细胞在牙周组织再生中的重要作用,以及Wnt/β - 连环蛋白信号通路参与这一过程,特别是细胞性牙骨质的附着。因此,控制该信号通路可以促进牙骨质再生,这是牙骨质 - PDL - 骨复合体再生的关键过程。本研究为细胞行为和信号通路提供了新的见解,将推动牙周组织再生的实际应用。