Wang Tao, Wang Shi-Kai, Chen Guo-Qing, Tian Wei-Dong
State Key Laboratory of Oral Disease, National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu 610041, China.
Department of Oral and Maxillofacial Surgery, West China Hospital of Stomatology, Sichuan University, Chengdu 610041, China.
Sichuan Da Xue Xue Bao Yi Xue Ban. 2020 Nov;51(6):735-741. doi: 10.12182/20201160101.
To investigate the role of a novel chemically defined medium (CDM) in the regulation of dental papilla cells (DPCs) functional phenotype in vitro and periodontal bone regeneration .
DPCs were isolated and cultured in conventional medium (CM) or CDM. The surface makers, and the proliferation, migration and osteogenic differentiation abilities of DPCs were evaluated. , the DPCs that mixed with collagen gel were implanted into the model rats in the defect of periodontal to repair the periodontal tissue. Regeneration of the tissues was examined by microcomputed tomography and histological observation.
DPCs in the CM group and CDM group showed similar surface markers. Compared to the CM group, the CDM significantly enhanced the proliferation, colony-forming efficiency and migration of DPCs . In addition, real time PCR showed that the expression levels of osteogenesis-related genes, 2, and . were significantly enhanced in DPCs in the CDM group. DPCs cells treated with CDM also exhibited higher alkaline phosphatase activity and stronger ability of formation of mineralized nodules , DPCs from CDM group significantly enhanced the periodontal bone regeneration and the reconstruction of periodontal bone tissues in rat periodontal defect model.
CDM is a suitable medium to culture DPCs for periodontal bone regeneration. This research provided a substitute for basic research and set the stage for future clinical application of stem cell transplantation.
探讨一种新型化学成分明确的培养基(CDM)在体外调节牙乳头细胞(DPCs)功能表型及牙周骨再生中的作用。
分离DPCs并在传统培养基(CM)或CDM中培养。评估DPCs的表面标志物、增殖、迁移和成骨分化能力。将与胶原凝胶混合的DPCs植入牙周缺损的模型大鼠体内以修复牙周组织。通过微型计算机断层扫描和组织学观察检查组织再生情况。
CM组和CDM组的DPCs显示出相似的表面标志物。与CM组相比,CDM显著增强了DPCs的增殖、集落形成效率和迁移能力。此外,实时聚合酶链反应显示,CDM组DPCs中成骨相关基因、2和的表达水平显著增强。用CDM处理的DPCs细胞还表现出更高的碱性磷酸酶活性和更强的矿化结节形成能力,CDM组的DPCs显著增强了大鼠牙周缺损模型中的牙周骨再生和牙周骨组织重建。
CDM是用于牙周骨再生培养DPCs的合适培养基。本研究为基础研究提供了替代方法,并为干细胞移植的未来临床应用奠定了基础。