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Deciduous dental pulp stem cells are involved in osteoclastogenesis during physiologic root resorption
Authors:Yuan Zhu  Linjuan Shang  Xiaoyan Chen  Xiangwei Kong  Na Liu  Yuyun Bai  Jun Fang  Jun Dang  Xiaojing Wang  Yan Jin
Institution:1. Research and Development Center for Tissue Engineering, Fourth Military Medical University, Xi'an, China;2. Department of Pediatric Dentistry, School of Stomatology, Fourth Military Medical University, Xi'an, China;3. Department of Pediatric Dentistry, Foshan Stomatology Hospital, Foshan, China;4. Department of Orthodontics, School of Stomatology, Fourth Military Medical University, Xi'an, China;5. Department of Stomatology, General Hospital of Chinese PLA, Beijing, China;6. Department of Oral Histology and Pathology, School of Stomatology, Fourth Military Medical University, Xi'an, China;7. Department of Periodontics, School of Stomatology, Fourth Military Medical University, Xi'an, China
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 (VD3), the RANKL/OPG ratio was reduced only with VD3. 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. J. Cell. Physiol. 228: 207–215, 2013. © 2012 Wiley Periodicals, Inc.
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