牙龈内阿米巴通过VAMP8/-3驱动的胞吐途径诱导牙龈细胞死亡、胶原分解和宿主免疫反应。

IF 2.9 3区 医学 Q3 IMMUNOLOGY
Infection and Immunity Pub Date : 2025-04-08 Epub Date: 2025-03-21 DOI:10.1128/iai.00005-25
Lea Rosenfeld, Nico Neumann, Xin Bao, Aysegül Adam, Arne S Schaefer
{"title":"牙龈内阿米巴通过VAMP8/-3驱动的胞吐途径诱导牙龈细胞死亡、胶原分解和宿主免疫反应。","authors":"Lea Rosenfeld, Nico Neumann, Xin Bao, Aysegül Adam, Arne S Schaefer","doi":"10.1128/iai.00005-25","DOIUrl":null,"url":null,"abstract":"<p><p>The protozoan <i>Entamoeba gingivalis</i> commonly colonizes anaerobic periodontal pockets, induces a severe innate immune response, invades gingival mucosa, and kills epithelial cells. <i>E. gingivalis</i> infection is associated with the common oral inflammatory disease periodontitis. DNA variants in vesicle-associated membrane proteins (VAMP) -3 and -8 genes are linked to increased periodontitis risk. These genes mediate host-pathogen interactions, including mucin exocytosis to form protective barriers and matrix metalloproteinase (MMP) secretion in intestinal amoebiasis caused by <i>Entamoeba histolytica</i>. This study aimed to investigate the roles of VAMP3/8 in gingival defense and <i>E. gingivalis</i> infection mechanisms. Clustered regularly interspaced short palindromic repeats (CRISPR)-Cas9 gene editing was used to create VAMP3/8-deficient gingival epithelial cells and fibroblasts. Functional analyses included immunofluorescence, enzyme-linked immunosorbent assay (ELISA), cytotoxicity, and collagenase assays. VAMP8 co-localized with mucins in gingival epithelial cells (gECs), and VAMP3 with MMPs in gingival fibroblasts. In gECs<i>, E. gingivalis</i> infection increased mucin (MUC1: 3.6×, MUC21: 14.4×) and interleukin secretion (IL-8, IL-1B: >6×, <i>P</i> = 0.019). <i>VAMP8</i> deficiency in gECs caused higher cell death (35% vs 4% in controls) with reduced exocytosis of mucins and interleukins. Likewise, <i>E. gingivalis</i>-induced VAMP8 translocation into lipid rafts was lost in VAMP8 knockout cells, validating the participation of VAMP8 in exocytosis. In wild-type but not VAMP3-deficient gingival fibroblasts, <i>E. gingivalis</i> strongly activated collagenases. <i>E. gingivalis</i> effects were more pathogenic than those of the oral anaerobic bacterium <i>Porphyromonas gingivalis. E. gingivalis</i> exploits VAMP8/3-driven exocytosis pathways, driving inflammation and tissue destruction, underscoring its role as a significant periodontal pathogen.</p>","PeriodicalId":13541,"journal":{"name":"Infection and Immunity","volume":" ","pages":"e0000525"},"PeriodicalIF":2.9000,"publicationDate":"2025-04-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11977317/pdf/","citationCount":"0","resultStr":"{\"title\":\"<i>Entamoeba gingivalis</i> induces gingival cell death, collagen breakdown, and host immune response via VAMP8/-3-driven exocytosis pathways.\",\"authors\":\"Lea Rosenfeld, Nico Neumann, Xin Bao, Aysegül Adam, Arne S Schaefer\",\"doi\":\"10.1128/iai.00005-25\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The protozoan <i>Entamoeba gingivalis</i> commonly colonizes anaerobic periodontal pockets, induces a severe innate immune response, invades gingival mucosa, and kills epithelial cells. <i>E. gingivalis</i> infection is associated with the common oral inflammatory disease periodontitis. DNA variants in vesicle-associated membrane proteins (VAMP) -3 and -8 genes are linked to increased periodontitis risk. These genes mediate host-pathogen interactions, including mucin exocytosis to form protective barriers and matrix metalloproteinase (MMP) secretion in intestinal amoebiasis caused by <i>Entamoeba histolytica</i>. This study aimed to investigate the roles of VAMP3/8 in gingival defense and <i>E. gingivalis</i> infection mechanisms. Clustered regularly interspaced short palindromic repeats (CRISPR)-Cas9 gene editing was used to create VAMP3/8-deficient gingival epithelial cells and fibroblasts. Functional analyses included immunofluorescence, enzyme-linked immunosorbent assay (ELISA), cytotoxicity, and collagenase assays. VAMP8 co-localized with mucins in gingival epithelial cells (gECs), and VAMP3 with MMPs in gingival fibroblasts. In gECs<i>, E. gingivalis</i> infection increased mucin (MUC1: 3.6×, MUC21: 14.4×) and interleukin secretion (IL-8, IL-1B: >6×, <i>P</i> = 0.019). <i>VAMP8</i> deficiency in gECs caused higher cell death (35% vs 4% in controls) with reduced exocytosis of mucins and interleukins. Likewise, <i>E. gingivalis</i>-induced VAMP8 translocation into lipid rafts was lost in VAMP8 knockout cells, validating the participation of VAMP8 in exocytosis. In wild-type but not VAMP3-deficient gingival fibroblasts, <i>E. gingivalis</i> strongly activated collagenases. <i>E. gingivalis</i> effects were more pathogenic than those of the oral anaerobic bacterium <i>Porphyromonas gingivalis. E. gingivalis</i> exploits VAMP8/3-driven exocytosis pathways, driving inflammation and tissue destruction, underscoring its role as a significant periodontal pathogen.</p>\",\"PeriodicalId\":13541,\"journal\":{\"name\":\"Infection and Immunity\",\"volume\":\" \",\"pages\":\"e0000525\"},\"PeriodicalIF\":2.9000,\"publicationDate\":\"2025-04-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11977317/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Infection and Immunity\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1128/iai.00005-25\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/3/21 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"IMMUNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Infection and Immunity","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1128/iai.00005-25","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/3/21 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

原生动物牙龈内阿米巴通常在厌氧牙周袋中定植,引起严重的先天免疫反应,侵入牙龈粘膜并杀死上皮细胞。牙龈杆菌感染与常见的口腔炎症性疾病牙周炎有关。囊泡相关膜蛋白(VAMP) -3和-8基因的DNA变异与牙周炎风险增加有关。在溶组织内阿米巴引起的肠阿米巴病中,这些基因介导宿主与病原体的相互作用,包括粘蛋白胞吐形成保护屏障和基质金属蛋白酶(MMP)的分泌。本研究旨在探讨VAMP3/8在牙龈防御中的作用和牙龈链球菌感染机制。集群规则间隔短回文重复(CRISPR)-Cas9基因编辑用于创建vamp3 /8缺陷的牙龈上皮细胞和成纤维细胞。功能分析包括免疫荧光、酶联免疫吸附测定(ELISA)、细胞毒性和胶原酶测定。VAMP8在牙龈上皮细胞(gec)中与粘蛋白共定位,VAMP3在牙龈成纤维细胞中与MMPs共定位。在gECs中,牙龈杆菌感染使黏液蛋白(MUC1: 3.6×, MUC21: 14.4×)和白细胞介素分泌(IL-8, IL-1B: bb6 ×, P = 0.019)升高。gECs中VAMP8缺乏导致更高的细胞死亡(35% vs对照组的4%),并减少粘蛋白和白细胞介素的胞吐。同样,在VAMP8敲除细胞中,牙龈杆菌诱导的VAMP8向脂筏的易位丢失,证实了VAMP8参与胞吐作用。在野生型而非vamp3缺失的牙龈成纤维细胞中,牙龈E. gingivalis强烈激活胶原酶。牙龈卟啉单胞菌的致病性高于口腔厌氧菌牙龈卟啉单胞菌。牙龈E. gingivalis利用vamp8 /3驱动的胞吐途径,驱动炎症和组织破坏,强调其作为重要的牙周病原体的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Entamoeba gingivalis induces gingival cell death, collagen breakdown, and host immune response via VAMP8/-3-driven exocytosis pathways.

The protozoan Entamoeba gingivalis commonly colonizes anaerobic periodontal pockets, induces a severe innate immune response, invades gingival mucosa, and kills epithelial cells. E. gingivalis infection is associated with the common oral inflammatory disease periodontitis. DNA variants in vesicle-associated membrane proteins (VAMP) -3 and -8 genes are linked to increased periodontitis risk. These genes mediate host-pathogen interactions, including mucin exocytosis to form protective barriers and matrix metalloproteinase (MMP) secretion in intestinal amoebiasis caused by Entamoeba histolytica. This study aimed to investigate the roles of VAMP3/8 in gingival defense and E. gingivalis infection mechanisms. Clustered regularly interspaced short palindromic repeats (CRISPR)-Cas9 gene editing was used to create VAMP3/8-deficient gingival epithelial cells and fibroblasts. Functional analyses included immunofluorescence, enzyme-linked immunosorbent assay (ELISA), cytotoxicity, and collagenase assays. VAMP8 co-localized with mucins in gingival epithelial cells (gECs), and VAMP3 with MMPs in gingival fibroblasts. In gECs, E. gingivalis infection increased mucin (MUC1: 3.6×, MUC21: 14.4×) and interleukin secretion (IL-8, IL-1B: >6×, P = 0.019). VAMP8 deficiency in gECs caused higher cell death (35% vs 4% in controls) with reduced exocytosis of mucins and interleukins. Likewise, E. gingivalis-induced VAMP8 translocation into lipid rafts was lost in VAMP8 knockout cells, validating the participation of VAMP8 in exocytosis. In wild-type but not VAMP3-deficient gingival fibroblasts, E. gingivalis strongly activated collagenases. E. gingivalis effects were more pathogenic than those of the oral anaerobic bacterium Porphyromonas gingivalis. E. gingivalis exploits VAMP8/3-driven exocytosis pathways, driving inflammation and tissue destruction, underscoring its role as a significant periodontal pathogen.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Infection and Immunity
Infection and Immunity 医学-传染病学
CiteScore
6.00
自引率
6.50%
发文量
268
审稿时长
3 months
期刊介绍: Infection and Immunity (IAI) provides new insights into the interactions between bacterial, fungal and parasitic pathogens and their hosts. Specific areas of interest include mechanisms of molecular pathogenesis, virulence factors, cellular microbiology, experimental models of infection, host resistance or susceptibility, and the generation of innate and adaptive immune responses. IAI also welcomes studies of the microbiome relating to host-pathogen interactions.
×
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:481959085
Book学术官方微信