Wakuda Shin, Hasuike Akira, Fujiwara Kyoko, Sakai Ryo, Chaurasia Akhilanand, Uchiyama Toshio, Sato Shuichi
Department of Periodontology, Nihon University School of Dentistry, Tokyo, Japan.
Division of Applied Oral Sciences, Nihon University Graduate School of Dentistry, Tokyo, Japan.
J Dent Sci. 2025 Jan;20(1):384-392. doi: 10.1016/j.jds.2024.06.013. Epub 2024 Jun 22.
BACKGROUND/PURPOSE: Peri-implantitis remains a substantial challenge. This study investigated the effect of titanium particles on human oral epithelial cells, focusing on the nucleotide-binding domain and leucine-rich repeat protein (NLRP) 3 inflammasome. MATERIALS AND METHODS: The Ca9-22 human gingival epithelial cell line was subjected to incubation with titanium particles. To evaluate cell viability, the MTT assay was employed. Total RNA was extracted, and messenger RNA (mRNA) expressions of , , , , , and were analyzed. The concentration of interleukin (IL)1β in cell supernatants was quantified through enzyme-linked immunosorbent assay. Intracellular reactive oxygen species (ROS) were visualized using an ROS assay Kit. RESULTS: Ca9-22 cells treated with titanium particles showed >75% cell viability across all concentrations tested, with consistent results. mRNA expressions of inflammation-related genes ( and ) significantly increased in a dose-dependent manner. The mRNA expression of and , as well as the secretion of IL1β, increased after 6-h incubation with titanium particles. Moreover, the ROS assay results showed increased production of ROS after treatment with titanium particles, whereas NLRP3 expression and IL1β secretion reduced after treatment with N-acetyl-l-cysteine (ROS scavenger). CONCLUSION: Our findings indicate that titanium particles possess a distinct ability to trigger the NLRP3 inflammasome, partly by producing ROS.
背景/目的:种植体周围炎仍然是一个重大挑战。本研究调查了钛颗粒对人口腔上皮细胞的影响,重点关注核苷酸结合结构域和富含亮氨酸重复序列蛋白(NLRP)3炎性小体。 材料与方法:将Ca9-22人牙龈上皮细胞系与钛颗粒一起孵育。采用MTT法评估细胞活力。提取总RNA,并分析 、 、 、 、 和 的信使核糖核酸(mRNA)表达。通过酶联免疫吸附测定法定量细胞上清液中白细胞介素(IL)-1β的浓度。使用活性氧(ROS)检测试剂盒观察细胞内ROS。 结果:在所有测试浓度下,用钛颗粒处理的Ca9-22细胞显示细胞活力>75%,结果一致。炎症相关基因( 和 )的mRNA表达呈剂量依赖性显著增加。与钛颗粒孵育6小时后, 和 的mRNA表达以及IL-1β的分泌增加。此外,ROS检测结果显示,用钛颗粒处理后ROS生成增加,而用N-乙酰-L-半胱氨酸(ROS清除剂)处理后NLRP3表达和IL-1β分泌减少。 结论:我们的研究结果表明,钛颗粒具有触发NLRP3炎性小体的独特能力,部分原因是通过产生活性氧。
Cell Mol Gastroenterol Hepatol. 2016-3-19
Immunol Invest. 2023-4
Int J Oral Sci. 2023-11-23
Periodontol 2000. 2024-2
Clin Oral Implants Res. 2023-12
Cancer Discov. 2023-7-7
Nat Rev Rheumatol. 2023-4
Clin Implant Dent Relat Res. 2023-8
J Transl Med. 2022-9-23