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Strontium (Sr) elicits odontogenic differentiation of human dental pulp stem cells (hDPSCs): A therapeutic role for Sr in dentine repair?

机译:锶(Sr)引发人牙髓干细胞(hDPSCs)的牙源性分化:Sr在牙本质修复中的治疗作用?

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Strontium (Sr) forms a significant component of dental restorative materials and although it is widely used in toothpastes, the biological effects of Sr on the dentine-pulp complex have not been investigated. In this first study, we characterise the Sr elicited effects on human dental pulp stem cells (hDPSC) in vitro using exogenously Sr added to culture medium, and bioavailable Sr derived from a novel bioactive glass (BG). The related mechanisms were also investigated. Our results indicate that low dose Sr (between 0.1 and 2.5 mM) induces proliferation and alkaline phosphatase (ALP) activity of hDPSCs, but has no effect on colony formation or cell migration. Sr at specific concentrations (1 and 2.5 mM) stimulated collagen formation and mineralisation of the hDPSC generated matrix. In addition, qRT-PCR, Western blotting and immunocytochemistry revealed that Sr regulates gene expression and the protein secretion of the odontogenic markers: dentine sialophosphoprotein (DSPP) and dentine matrix protein 1 (DMP-1) and protein localisation (DSPP was localised to the Golgi, while no apparent changes occur in DMP-1 distribution which remains in both cytosol and the nucleus). Additionally, the calcium sensing receptor (CaSR) and downstream pathway MAPK/ERK signalling pathway in hDPSCs were activated by Sr. Bioavailable Sr from the BG revealed novel biological insights of regulating metabolic and ALP activities in hDPSCs. Taken together, these results suggest that Sr at specific doses significantly influences proliferation, odontogenic differentiation and mineralisation of hDPSCs in vitro via the CaSR using a pathway with similarities to osteoblast differentiation. These are the first such studies and indicate that Sr treatment of hDPSCs could be a promising therapeutic agent in dental applications. In conclusion, we propose that Sr from a substituted BG could be used more effectively in biomaterials designed for dental applications.
机译:锶(Sr)构成牙齿修复材料的重要组成部分,尽管它广泛用于牙膏中,但尚未研究Sr对牙本质-纸浆复合物的生物学作用。在这项首次研究中,我们使用添加到培养基中的外源Sr和衍生自新型生物活性玻璃(BG)的可生物利用的Sr表征了Sr在体外对人牙髓干细胞(hDPSC)引起的作用。还研究了相关机制。我们的结果表明,低剂量的Sr(介于0.1和2.5 mM之间)可诱导hDPSC的增殖和碱性磷酸酶(ALP)活性,但对菌落形成或细胞迁移没有影响。特定浓度(1和2.5 mM)的Sr刺激胶原蛋白的形成和hDPSC生成基质的矿化。此外,qRT-PCR,Western印迹和免疫细胞化学显示,Sr调节基因表达和牙源性标记物的蛋白质分泌:牙本质唾液磷蛋白(DSPP)和牙本质基质蛋白1(DMP-1)和蛋白质定位(DSPP定位于高尔基体,虽然DMP-1分布没有明显变化,但DMP-1分布仍然存在于细胞质和细胞核中。此外,hDPSCs中的钙敏感受体(CaSR)和下游途径MAPK / ERK信号传导途径被Sr激活。来自BG的生物可利用Sr揭示了调节hDPSCs代谢和ALP活性的新生物学见解。综上,这些结果表明,特定剂量的Sr通过与成骨细胞分化相似的途径,通过CaSR在体外显着影响hDPSC的增殖,成牙细胞分化和矿化。这些是第一个此类研究,表明hDPSCs的Sr治疗可能是牙科应用中有希望的治疗剂。总之,我们建议将来自取代BG的Sr可以更有效地用于为牙科应用设计的生物材料中。

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