Dextran sulfate sodium-induced colitis exacerbates periodontitis via the NADPH oxidase 2/reactive oxygen species axis in M1-like macrophages

hLife Pub Date : 2025-04-01 DOI:10.1016/j.hlife.2025.01.006
Tiansong Xu , Liqi Zhang , Murong Li , He Zhu , Ying Ni , Cancan Huang , Peihui Zou , Jie Zhang , Qian Zhang , Zhong Zheng , Chenggang Duan , Feng Chen
{"title":"Dextran sulfate sodium-induced colitis exacerbates periodontitis via the NADPH oxidase 2/reactive oxygen species axis in M1-like macrophages","authors":"Tiansong Xu ,&nbsp;Liqi Zhang ,&nbsp;Murong Li ,&nbsp;He Zhu ,&nbsp;Ying Ni ,&nbsp;Cancan Huang ,&nbsp;Peihui Zou ,&nbsp;Jie Zhang ,&nbsp;Qian Zhang ,&nbsp;Zhong Zheng ,&nbsp;Chenggang Duan ,&nbsp;Feng Chen","doi":"10.1016/j.hlife.2025.01.006","DOIUrl":null,"url":null,"abstract":"<div><div>Periodontitis is associated with various systemic diseases, among the most important of which is inflammatory bowel disease (IBD). However, the mechanisms by which IBD exacerbates periodontitis remain unclear. Activation of the nicotinamide adenine dinucleotide phosphate (NADPH) oxidase 2 (NOX2)/reactive oxygen species (ROS) axis in macrophages can worsen intestinal inflammation and periodontitis. Nonetheless, whether IBD aggravates periodontitis by activating the NOX2/ROS axis, specifically in oral macrophages is unknown. In this study, we established animal models and analyzed single-cell RNA data to investigate these pathogenic pathways. Periodontal inflammation was exacerbated <em>via</em> the NOX2/ROS pathway in tumor necrosis factor M1-like macrophages during colitis. Notably, when a NOX2 inhibitor was administered, resulting in reduced ROS expression in periodontal tissue, both periodontal and intestinal inflammation were significantly alleviated, and disruption of the periodontal and intestinal microbiota was reduced. By uncovering the pathogenic pathways linking these two diseases, this study provides insight into potential treatments for periodontitis and related systemic conditions.</div></div>","PeriodicalId":100609,"journal":{"name":"hLife","volume":"3 4","pages":"Pages 187-200"},"PeriodicalIF":0.0000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"hLife","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2949928325000069","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Periodontitis is associated with various systemic diseases, among the most important of which is inflammatory bowel disease (IBD). However, the mechanisms by which IBD exacerbates periodontitis remain unclear. Activation of the nicotinamide adenine dinucleotide phosphate (NADPH) oxidase 2 (NOX2)/reactive oxygen species (ROS) axis in macrophages can worsen intestinal inflammation and periodontitis. Nonetheless, whether IBD aggravates periodontitis by activating the NOX2/ROS axis, specifically in oral macrophages is unknown. In this study, we established animal models and analyzed single-cell RNA data to investigate these pathogenic pathways. Periodontal inflammation was exacerbated via the NOX2/ROS pathway in tumor necrosis factor M1-like macrophages during colitis. Notably, when a NOX2 inhibitor was administered, resulting in reduced ROS expression in periodontal tissue, both periodontal and intestinal inflammation were significantly alleviated, and disruption of the periodontal and intestinal microbiota was reduced. By uncovering the pathogenic pathways linking these two diseases, this study provides insight into potential treatments for periodontitis and related systemic conditions.

Abstract Image

葡聚糖硫酸钠诱导的结肠炎通过m1样巨噬细胞NADPH氧化酶2/活性氧轴加重牙周炎
牙周炎与多种全身性疾病有关,其中最重要的是炎症性肠病(IBD)。然而,IBD 加剧牙周炎的机制仍不清楚。巨噬细胞中的烟酰胺腺嘌呤二核苷酸磷酸(NADPH)氧化酶 2(NOX2)/活性氧(ROS)轴的激活会加重肠道炎症和牙周炎。然而,IBD 是否会通过激活 NOX2/ROS 轴,特别是口腔巨噬细胞中的 NOX2/ROS 轴而加重牙周炎,目前尚不清楚。在这项研究中,我们建立了动物模型并分析了单细胞 RNA 数据,以研究这些致病途径。在结肠炎期间,牙周炎症通过肿瘤坏死因子 M1 样巨噬细胞中的 NOX2/ROS 通路而加剧。值得注意的是,当服用 NOX2 抑制剂导致牙周组织中的 ROS 表达减少时,牙周和肠道炎症都会明显缓解,牙周和肠道微生物群的破坏也会减少。通过揭示连接这两种疾病的致病途径,这项研究为牙周炎和相关系统性疾病的潜在治疗方法提供了启示。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信