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":"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","authors":"Tiansong Xu , Liqi Zhang , Murong Li , He Zhu , Ying Ni , Cancan Huang , Peihui Zou , Jie Zhang , Qian Zhang , Zhong Zheng , Chenggang Duan , 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":"{\"title\":\"Dextran sulfate sodium-induced colitis exacerbates periodontitis via the NADPH oxidase 2/reactive oxygen species axis in M1-like macrophages\",\"authors\":\"Tiansong Xu , Liqi Zhang , Murong Li , He Zhu , Ying Ni , Cancan Huang , Peihui Zou , Jie Zhang , Qian Zhang , Zhong Zheng , Chenggang Duan , 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}","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}
Dextran sulfate sodium-induced colitis exacerbates periodontitis via the NADPH oxidase 2/reactive oxygen species axis in M1-like macrophages
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.