Department of Biomedical Sciences, Texas A&M University College of Dentistry, Dallas, TX, USA.
State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, Department of Periodontics, West China Hospital of Stomatology, Sichuan University, Chengdu, Sichuan, China.
J Dent Res. 2021 Oct;100(11):1289-1298. doi: 10.1177/00220345211007429. Epub 2021 Apr 14.
Cementum, a specialized bony layer covering an entire molar root surface, anchors teeth into alveolar bone. Gli1, a key transcriptional activator in Hedgehog signaling, has been identified as a mesenchymal progenitor cell marker in various tissues, including the periodontal ligament (PDL). To address the mechanisms by which Gli1 progenitor cells contribute to cementogenesis, we used the knock-in line to mark Gli1 progenitors and the ; line (named ) to trace Gli1 progeny cells during cementogenesis. Our data unexpectedly displayed a biphasic feature of Gli1 PDL progenitor cells and cementum growth: a negative relationship between Gli1 progenitor cell number and cementogenesis but a positive correlation between Gli1-derived acellular and cellular cementoblast cell number and cementum growth. DTA-ablation of Gli1 cells led to a cementum hypoplasia, including a significant reduction of both acellular and cellular cementoblast cells. Gain-of-function studies (by constitutive stabilization of β-catenin in Gli1 cells) revealed a cementum hyperplasia. A loss of function (by conditional deletion of β-catenin in Gli1 cells) resulted in a reduction of postnatal cementum growth. Together, our studies support a vital role of Gli1 progenitor cells in contribution to both types of cementum, in which canonical Wnt/β-catenin signaling positively regulates the differentiation of Gli1 progenitors to cementoblasts during cementogenesis.
牙骨质是覆盖整个磨牙根表面的一种特殊骨层,将牙齿固定在牙槽骨中。Gli1 是 Hedgehog 信号通路中的关键转录激活因子,已被鉴定为包括牙周韧带(PDL)在内的各种组织中的间充质祖细胞标志物。为了研究 Gli1 祖细胞在成牙骨质中的作用机制,我们使用了敲入系来标记 Gli1 祖细胞和 ; 系(命名为 )来追踪成牙骨质过程中的 Gli1 祖细胞后代。我们的数据出人意料地显示了 Gli1 PDL 祖细胞和成牙骨质的双峰特征:Gli1 祖细胞数量与成牙骨质呈负相关,但无细胞和有细胞成牙骨质细胞数量与成牙骨质生长呈正相关。Gli1 细胞的 DTA 消融导致牙骨质发育不全,包括无细胞和成牙骨质细胞数量的显著减少。过表达研究(通过在 Gli1 细胞中稳定表达 β-catenin)显示牙骨质增生。功能丧失(通过条件性删除 Gli1 细胞中的 β-catenin)导致出生后牙骨质生长减少。总之,我们的研究支持 Gli1 祖细胞在两种类型的牙骨质形成中的重要作用,其中经典 Wnt/β-catenin 信号通路正向调节 Gli1 祖细胞在成牙骨质过程中向成牙骨质细胞的分化。