文献检索文档翻译深度研究
Suppr Zotero 插件Zotero 插件
邀请有礼套餐&价格历史记录

新学期,新优惠

限时优惠:9月1日-9月22日

30天高级会员仅需29元

1天体验卡首发特惠仅需5.99元

了解详情
不再提醒
插件&应用
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
高级版
套餐订阅购买积分包
AI 工具
文献检索文档翻译深度研究
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2025

钛颗粒诱导人牙龈上皮细胞中的炎性小体

Titanium particle-induced inflammasome in human gingival epithelial cells.

作者信息

Wakuda Shin, Hasuike Akira, Fujiwara Kyoko, Sakai Ryo, Chaurasia Akhilanand, Uchiyama Toshio, Sato Shuichi

机构信息

Department of Periodontology, Nihon University School of Dentistry, Tokyo, Japan.

Division of Applied Oral Sciences, Nihon University Graduate School of Dentistry, Tokyo, Japan.

出版信息

J Dent Sci. 2025 Jan;20(1):384-392. doi: 10.1016/j.jds.2024.06.013. Epub 2024 Jun 22.


DOI:10.1016/j.jds.2024.06.013
PMID:39873089
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11762583/
Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76eb/11762583/c47242a722a9/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76eb/11762583/89779b69ca7f/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76eb/11762583/fd31d40b5715/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76eb/11762583/ed342ea117eb/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76eb/11762583/c47242a722a9/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76eb/11762583/89779b69ca7f/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76eb/11762583/fd31d40b5715/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76eb/11762583/ed342ea117eb/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76eb/11762583/c47242a722a9/gr4.jpg

相似文献

[1]
Titanium particle-induced inflammasome in human gingival epithelial cells.

J Dent Sci. 2025-1

[2]
Wear Particle-induced Priming of the NLRP3 Inflammasome Depends on Adherent Pathogen-associated Molecular Patterns and Their Cognate Toll-like Receptors: An In Vitro Study.

Clin Orthop Relat Res. 2018-12

[3]
Reactive oxygen species activated NLRP3 inflammasomes prime environment-induced murine dry eye.

Exp Eye Res. 2014-5-14

[4]
Titanium Ions Play a Synergistic Role in the Activation of NLRP3 Inflammasome in Jurkat T Cells.

Inflammation. 2020-8

[5]
NOD-Like Receptor Protein 3 Inflammasome Priming and Activation in Barrett's Epithelial Cells.

Cell Mol Gastroenterol Hepatol. 2016-3-19

[6]
Reactive oxygen species activated NLRP3 inflammasomes initiate inflammation in hyperosmolarity stressed human corneal epithelial cells and environment-induced dry eye patients.

Exp Eye Res. 2015-5

[7]
Helicobacter pylori induces IL-1β and IL-18 production in human monocytic cell line through activation of NLRP3 inflammasome via ROS signaling pathway.

Pathog Dis. 2015-6

[8]
Mechanisms that lead to the regulation of NLRP3 inflammasome expression and activation in human dental pulp fibroblasts.

Mol Immunol. 2015-8

[9]
Genetic and Epigenetic Regulation of the Innate Immune Response to Gout.

Immunol Invest. 2023-4

[10]
Ginsenoside Rg1 attenuates lipopolysaccharide-induced chronic liver damage by activating Nrf2 signaling and inhibiting inflammasomes in hepatic cells.

J Ethnopharmacol. 2024-4-24

本文引用的文献

[1]
Crosstalk between inflammasome sensors and DNA damage response pathways.

FEBS J. 2024-9

[2]
Titanium particles in peri-implantitis: distribution, pathogenesis and prospects.

Int J Oral Sci. 2023-11-23

[3]
Emerging factors affecting peri-implant bone metabolism.

Periodontol 2000. 2024-2

[4]
Inflammasomes NLRP3 and AIM2 in peri-implantitis: A cross-sectional study.

Clin Oral Implants Res. 2023-12

[5]
The DNA Damage Response and Inflammation in Cancer.

Cancer Discov. 2023-7-7

[6]
Osteoimmune regulation underlies oral implant osseointegration and its perturbation.

Front Immunol. 2022

[7]
Inflammation and DNA damage: cause, effect or both.

Nat Rev Rheumatol. 2023-4

[8]
Physiopathology of peri-implant diseases.

Clin Implant Dent Relat Res. 2023-8

[9]
Host-microbiome interactions regarding peri-implantitis and dental implant loss.

J Transl Med. 2022-9-23

[10]
Clinical Evaluation of the Relationship Between Systemic Disease and the Time of Onset of Peri-Implantitis: A Retrospective Cohort Study.

J Oral Implantol. 2023-2-1

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

推荐工具

医学文档翻译智能文献检索