牙髓干细胞
细胞生物学
骨钙素
骨桥蛋白
Wnt信号通路
细胞外基质
干细胞
牙本质涎磷蛋白
化学
运行x2
细胞分化
碱性磷酸酶
信号转导
生物
免疫学
生物化学
酶
基因
作者
Nanxin Liu,Mi Zhou,Qi Zhang,Tao Zhang,Taoran Tian,Quanquan Ma,Changyue Xue,Shiyu Lin,Xiaoxiao Cai
摘要
Abstract Objectives Researches showed that stiffness of the extracellular matrix can affect the differentiation of many stem cells. Dental pulp stem cells ( DPSC s) are a promising type of adult stem cell. However, we know little about whether and how the behaviour of DPSC s is influenced by stiffness. Materials and methods We carried out a study that cultured DPSC s on tunable elasticity polydimethylsiloxane substrates to investigate the influence on morphology, proliferation, osteogenic/odontogenic differentiation and its possible mechanism. Results Soft substrates changed the cell morphology and inhibited the proliferation of DPSC s. Expression of markers related to osteogenic/odontogenic differentiation was significantly increased as the substrate stiffness increased, including ALP (alkaline phosphatase), OCN (osteocalcin), OPN (osteopontin), RUNX ‐2 (runt‐related transcription factor‐2), BMP ‐2 (bone morphogenetic protein‐2), DSPP (dentin sialophosphoprotein) and DMP ‐1 (dentin matrix protein‐1). Mechanical properties promote the function of DPSC s related to the Wnt signalling pathway. Conclusions Our results showed that mechanical factors can regulate the proliferation and differentiation of DPSC s via the WNT signalling pathway. This provides theoretical basis to optimize dental or bone tissue regeneration through increasing stiffness of extracelluar matrix.
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