School of Dentistry, China Medical University, Taichung, Taiwan.
School of Dentistry, China Medical University, Taichung, Taiwan; Graduate Institute of Clinical Medical Science, China Medical University, Taichung, Taiwan; Department of Pediatric Dentistry, China Medical University Hospital, Taichung, Taiwan.
J Formos Med Assoc. 2019 Oct;118(10):1458-1465. doi: 10.1016/j.jfma.2019.07.010. Epub 2019 Jul 26.
BACKGROUND/PURPOSE: Mineral trioxide aggregate (Pro-Root MTA, PR-MTA) and bioceramics (iRoot SP Injectable Root Canal Sealer, iR-BC) are used for making apical plugs used in apexification, repairing root perforations during root canal therapy, and treating internal root resorption. The purpose of the present in vitro study was to compare the biological effects of PR-MTA- and iR-BC-based dental sealers in the mouse macrophage cell line RAW 264.7.
Cytotoxicity and cell proliferation were analyzed using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay and cell hemocytometer, respectively. Protein expression of biomarkers of cell proliferation, autophagy, and osteoclast differentiation was determined by western blotting. Pro-inflammatory gene expression was examined using quantitative reverse transcription-PCR.
PR-MTA induced cytotoxicity in RAW 264.7 cells in a dose-dependent manner, and iR-BC was more cytotoxic than PR-MTA. Low-dose and short-term treatments of both PR-MTA and iR-BC induced RAW 264.7 cell proliferation. PR-MTA induced autophagy, whereas iR-BC did not. Neither PR-MTA nor iR-BC induced osteoclastogenesis. Pro-inflammatory genes were activated by both materials. However, the expression of inducible nitric oxide synthase (iNOS) mRNA was upregulated by iR-BC treatment, but not by PR-MTA treatment.
Overall, dental PR-MTA and iR-BC induced pro-inflammatory genes but did not induce osteoclastogenesis in macrophages. PR-MTA and iR-BC induced M2 and M1 polarization, respectively, of RAW 264.7 cells.
背景/目的:矿化三氧化物凝聚体(Pro-Root MTA,PR-MTA)和生物陶瓷(iRoot SP 根管内注射用密封剂,iR-BC)用于制作根尖封闭剂,用于根尖诱导成形术,修复根管治疗期间的根管穿孔,并治疗内吸收。本体外研究的目的是比较 PR-MTA 和 iR-BC 基牙科密封剂对 RAW 264.7 小鼠巨噬细胞系的生物学影响。
采用 3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)法和细胞血球计数器分别分析细胞毒性和细胞增殖。通过蛋白质印迹法测定细胞增殖、自噬和破骨细胞分化的生物标志物的蛋白表达。使用定量逆转录 PCR 检测促炎基因的表达。
PR-MTA 以剂量依赖性方式诱导 RAW 264.7 细胞的细胞毒性,而 iR-BC 比 PR-MTA 更具细胞毒性。PR-MTA 和 iR-BC 的低剂量和短期处理均诱导 RAW 264.7 细胞增殖。PR-MTA 诱导自噬,而 iR-BC 则没有。PR-MTA 和 iR-BC 均未诱导破骨细胞生成。两种材料均激活促炎基因。然而,iR-BC 处理上调诱导型一氧化氮合酶(iNOS)mRNA 的表达,但 PR-MTA 处理则没有。
总体而言,牙科 PR-MTA 和 iR-BC 诱导了巨噬细胞中的促炎基因,但未诱导破骨细胞生成。PR-MTA 和 iR-BC 分别诱导 RAW 264.7 细胞的 M2 和 M1 极化。