Chumpraman Apisit, Tannukit Sissada, Chotigeat Wilaiwan, Kedjarune-Leggat Ureporn
Department of Oral Biology and Occlusion, Faculty of Dentistry, Prince of Songkla University, Songkhla, Thailand.
Cell Biology and Biomaterial Research Unit, Faculty of Dentistry, Prince of Songkla University, Songkhla, Thailand.
J Dent Sci. 2023 Jul;18(3):1055-1061. doi: 10.1016/j.jds.2022.11.024. Epub 2022 Dec 5.
BACKGROUND/PURPOSE: Fortilin is a multi-functional protein involved in several cellular processes. It has been shown promising potential to be a bioactive molecule that can be incorporated in the dental materials. This study aimed to compare the biocompatibility and mineralization activities of modified glass ionomer cement (Bio-GIC) and Biodentine by direct and indirect method on human dental pulp stem cells (hDPSCs).
Conventional glass ionomer cement (GIC), Bio-GIC (GIC supplemented with chitosan, tricalcium phosphate, and recombinant fortilin from ), and Biodentine were examined in this study. Recombinant fortilin was purified and tested for its cytotoxicity by 3-[4,5-dimethylthiazol-2-yl]-2,5 diphenyltetrazolium bromide (MTT) assay. Human DPSCs were treated with different material eluate for particular time intervals. At given time points, viability of hDPSCs was examined using MTT assay and calcium deposition was assessed by Alizarin red staining assay. Comparisons of the data among groups were analyzed by analysis of variance and Tukey's multiple comparisons.
All test materials demonstrated no cytotoxicity. In addition, Bio-GIC promoted cell proliferation at 72 h. For direct and indirect method, cells treated with Bio-GIC demonstrated significantly higher calcium deposition than other groups ( < 0.05).
Bio-GIC and Biodentine are not cytotoxic to hDPSCs. Bio-GIC demonstrates enhanced calcium deposition comparable to Biodentine. Bio-GIC may be further developed as a bioactive material for dentin regeneration.
背景/目的:富田蛋白是一种参与多种细胞过程的多功能蛋白质。它已显示出作为一种可掺入牙科材料中的生物活性分子的潜在前景。本研究旨在通过直接和间接方法比较改性玻璃离子水门汀(Bio-GIC)和生物活性牙本质对人牙髓干细胞(hDPSC)的生物相容性和矿化活性。
本研究检测了传统玻璃离子水门汀(GIC)、Bio-GIC(添加了壳聚糖、磷酸三钙和重组富田蛋白的GIC)和生物活性牙本质。对重组富田蛋白进行纯化,并通过3-[4,5-二甲基噻唑-2-基]-2,5-二苯基四氮唑溴盐(MTT)法检测其细胞毒性。将人牙髓干细胞用不同材料洗脱液处理特定时间间隔。在给定时间点,使用MTT法检测hDPSC的活力,并通过茜素红染色法评估钙沉积。组间数据比较采用方差分析和Tukey多重比较。
所有测试材料均未显示细胞毒性。此外,Bio-GIC在72小时时促进细胞增殖。对于直接和间接方法,用Bio-GIC处理的细胞显示出比其他组显著更高的钙沉积(P<0.05)。
Bio-GIC和生物活性牙本质对hDPSC无细胞毒性。Bio-GIC显示出与生物活性牙本质相当的增强的钙沉积。Bio-GIC可进一步开发为用于牙本质再生的生物活性材料。