Miyano Yuko, Mikami Masato, Katsuragi Hiroaki, Shinkai Koichi
Advanced Operative Dentistry-Endodontics, The Nippon Dental University Graduate School of Life Dentistry at Niigata, Nigata, Japan.
Department of Microbiology, The Nippon Dental University School of Life Dentistry at Niigata, Nigata, Japan.
Biol Trace Elem Res. 2023 Dec;201(12):5585-5600. doi: 10.1007/s12011-023-03625-z. Epub 2023 Mar 14.
This study aimed to clarify the effects of strontium (Sr), borate (BO), and silicate (SiO) on cell proliferative capacity, the induction of differentiation into odontoblast-like cells (OLCs), and substrate formation of human dental pulp stem cells (hDPSCs). Sr, BO, and SiO solutions were added to the hDPSC culture medium at three different concentrations, totaling nine experimental groups. The effects of these ions on hDPSC proliferation, calcification, and collagen formation after 14, 21, and 28 days of culture were evaluated using a cell proliferation assay, a quantitative alkaline phosphatase (ALP) activity assay, and Alizarin Red S and Sirius Red staining, respectively. Furthermore, the effects of these ions on hDPSC differentiation into OLCs were assessed via quantitative polymerase chain reaction and immunocytochemistry. Sr and SiO increased the expression of odontoblast markers; i.e., nestin, dentin matrix protein-1, dentin sialophosphoprotein, and ALP genes, compared with the control group. BO increased the ALP gene expression and activity. The results of this study suggested that Sr, BO, and SiO may induce hDPSC differentiation into OLCs.
本研究旨在阐明锶(Sr)、硼酸盐(BO)和硅酸盐(SiO)对人牙髓干细胞(hDPSC)的细胞增殖能力、诱导分化为成牙本质样细胞(OLC)以及基质形成的影响。将Sr、BO和SiO溶液以三种不同浓度添加到hDPSC培养基中,共九个实验组。分别使用细胞增殖测定、定量碱性磷酸酶(ALP)活性测定以及茜素红S和天狼星红染色,评估这些离子在培养14、21和28天后对hDPSC增殖、钙化和胶原形成的影响。此外,通过定量聚合酶链反应和免疫细胞化学评估这些离子对hDPSC分化为OLC的影响。与对照组相比,Sr和SiO增加了成牙本质细胞标志物的表达,即巢蛋白、牙本质基质蛋白-1、牙本质涎磷蛋白和ALP基因。BO增加了ALP基因表达和活性。本研究结果表明,Sr、BO和SiO可能诱导hDPSC分化为OLC。