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有研究表明,在生理性牙根吸收过程中,恒牙牙髓干细胞参与破骨细胞的生成。

Deciduous dental pulp stem cells are involved in osteoclastogenesis during physiologic root resorption.

机构信息

Research and Development Center for Tissue Engineering, Fourth Military Medical University, Xi'an, China.

出版信息

J Cell Physiol. 2013 Jan;228(1):207-15. doi: 10.1002/jcp.24122.

DOI:10.1002/jcp.24122
PMID:22674471
Abstract

Multipotent mesenchymal stem cells are derived from the dental pulps of permanent teeth and exfoliated deciduous teeth, and are known to induce bone and dentin generation. However, the role of deciduous dental pulp stem cells (DDPSCs) in physiologic root resorption remains unclear. In this study, dental pulp stem cells (DPSCs) in permanent teeth (P) were retrieved and compared to DDPSCs from deciduous incisors at different root resorption stages: stable (S), middle (M), and final (F). Decalcified teeth sections showed that osteoclasts and resorption lacunae were most prevalent in the M resorption stage. DDPSC proliferation rate was also highest in the M stage. DDPSCs in the F stage produced more calcified nodules than those in the S or M stages. Alkaline phosphatase (ALP) expression was highest in the F stage, indicating that DDPSCs promote mineralization. In addition, the ratio of receptor activator of nuclear factor kappa B ligand (RANKL) and osteoprotegerin (OPG) expression was significantly higher in the M stage, indicating that DDPSCs promote resorption. Dickkopf 1 (Dkk1) expression was remarkably higher in the F and P groups, suggesting that the Wnt pathway is inhibited during the resorption process. Interestingly, despite the fact that Wnt3a down-regulated OPG in osteogenic induction medium and up-regulated RANKL in medium with 1,25-dihydroxy vitamin D3 (VD(3) ), the RANKL/OPG ratio was reduced only with VD(3) . Collectively, our data indicate that DDPSCs influence osteoclastogenesis during the physiologic root resorption process, and that the canonical Wnt pathway can change the RANKL/OPG expression ratio in DDPSCs.

摘要

多能间充质干细胞来源于恒牙和脱落乳牙的牙髓,已知其能诱导骨和牙本质生成。然而,脱落乳牙牙髓干细胞(DDPSC)在生理性牙根吸收中的作用尚不清楚。在这项研究中,我们从恒牙(P)牙髓中获取牙髓干细胞(DPSC),并与不同牙根吸收阶段的乳牙切牙(DDPSC)进行比较:稳定期(S)、中期(M)和末期(F)。脱钙牙切片显示,破骨细胞和吸收陷窝在 M 吸收期最为常见。M 期 DDPSC 增殖率也最高。F 期的 DDPSC 形成的钙化结节比 S 期或 M 期多。碱性磷酸酶(ALP)在 F 期表达最高,表明 DDPSC 促进矿化。此外,M 期核因子κ B 受体激活剂配体(RANKL)和骨保护素(OPG)表达的比值显著升高,表明 DDPSC 促进吸收。F 期和 P 期的 Dickkopf 1(Dkk1)表达显著升高,提示 Wnt 通路在吸收过程中受到抑制。有趣的是,尽管 Wnt3a 在成骨诱导培养基中下调 OPG,在 1,25-二羟维生素 D3(VD3)培养基中上调 RANKL,但只有 VD3 能降低 RANKL/OPG 比值。综上,我们的数据表明,DDPSC 在生理性牙根吸收过程中影响破骨细胞生成,经典 Wnt 通路可以改变 DDPSC 中 RANKL/OPG 的表达比值。

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