{"title":"巨噬细胞介导的三维人口腔黏膜模型中种植体相关生物膜的控制","authors":"Shuli Chen , Muhammad Imran Rahim , Carina Mikolai , Daniela Paasch , Andreas Winkel , Katharina Doll-Nikutta , Nico Lachmann , Henning Menzel , Dagmar Wirth , Hansjörg Hauser , Meike Stiesch","doi":"10.1016/j.mtla.2025.102452","DOIUrl":null,"url":null,"abstract":"<div><div>Macrophages are pivotal in regulating inflammation and facilitating pathogen clearance, particularly in peri-implant environments prone to biofilm infections. For a better understanding of the role of these immune cells in host-biofilm-implant interactions, we developed a complex three-dimensional (3D) implant-tissue-oral-bacterial-biofilm model (INTER<sub>b</sub>ACT) with integrated macrophages to mimic the intricate triangular interactions between implant materials, biofilms, and the host, in conditions simulating the <em>in vivo</em> environment. The INTER<sub>b</sub>ACT model includes a peri-implant mucosa with collagen-embedded fibroblasts and macrophages, overlaid with a multi-layered oral epithelium, as well as a multi-species biofilm. Histological analysis demonstrated a preserved peri-implant architecture with high cell viability. Co-cultivation with multi-species biofilms provided valuable insights into macrophage roles in pathogen defence and inflammation regulation. In tissues lacking macrophages, biofilm exposure led to compromised epithelial integrity, whereas macrophage-containing tissues maintained their epithelial structure. Macrophages significantly reduced the biofilm biomass while promoting bacterial death. Inflammatory cytokine levels elevated under sterile conditions decreased upon biofilm exposure, suggesting a biofilm-mediated immune suppression. Cytokine expression levels differentially reacted to biofilm exposure and macrophage concentration, with IL-1β and IL-17 levels notably elevated in biofilm-exposed tissues, aligning with clinical observations of peri-implant inflammation. Our findings demonstrate that the INTER<sub>b</sub>ACT model, after incorporation of macrophages, serves as a physiologically relevant platform for studying host-pathogen dynamics and allows to identify key inflammatory markers associated with biofilm-related complications. Furthermore, this model holds significant potential for evaluating novel therapeutic strategies, such as sensor-actuator systems to detect and combat pathogenic biofilms, improving clinical outcomes in peri-implantitis management.</div></div>","PeriodicalId":47623,"journal":{"name":"Materialia","volume":"41 ","pages":"Article 102452"},"PeriodicalIF":3.0000,"publicationDate":"2025-05-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Macrophage-mediated control of implant-associated biofilms in a three-dimensional human oral mucosa model\",\"authors\":\"Shuli Chen , Muhammad Imran Rahim , Carina Mikolai , Daniela Paasch , Andreas Winkel , Katharina Doll-Nikutta , Nico Lachmann , Henning Menzel , Dagmar Wirth , Hansjörg Hauser , Meike Stiesch\",\"doi\":\"10.1016/j.mtla.2025.102452\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Macrophages are pivotal in regulating inflammation and facilitating pathogen clearance, particularly in peri-implant environments prone to biofilm infections. For a better understanding of the role of these immune cells in host-biofilm-implant interactions, we developed a complex three-dimensional (3D) implant-tissue-oral-bacterial-biofilm model (INTER<sub>b</sub>ACT) with integrated macrophages to mimic the intricate triangular interactions between implant materials, biofilms, and the host, in conditions simulating the <em>in vivo</em> environment. The INTER<sub>b</sub>ACT model includes a peri-implant mucosa with collagen-embedded fibroblasts and macrophages, overlaid with a multi-layered oral epithelium, as well as a multi-species biofilm. Histological analysis demonstrated a preserved peri-implant architecture with high cell viability. Co-cultivation with multi-species biofilms provided valuable insights into macrophage roles in pathogen defence and inflammation regulation. In tissues lacking macrophages, biofilm exposure led to compromised epithelial integrity, whereas macrophage-containing tissues maintained their epithelial structure. Macrophages significantly reduced the biofilm biomass while promoting bacterial death. Inflammatory cytokine levels elevated under sterile conditions decreased upon biofilm exposure, suggesting a biofilm-mediated immune suppression. Cytokine expression levels differentially reacted to biofilm exposure and macrophage concentration, with IL-1β and IL-17 levels notably elevated in biofilm-exposed tissues, aligning with clinical observations of peri-implant inflammation. Our findings demonstrate that the INTER<sub>b</sub>ACT model, after incorporation of macrophages, serves as a physiologically relevant platform for studying host-pathogen dynamics and allows to identify key inflammatory markers associated with biofilm-related complications. Furthermore, this model holds significant potential for evaluating novel therapeutic strategies, such as sensor-actuator systems to detect and combat pathogenic biofilms, improving clinical outcomes in peri-implantitis management.</div></div>\",\"PeriodicalId\":47623,\"journal\":{\"name\":\"Materialia\",\"volume\":\"41 \",\"pages\":\"Article 102452\"},\"PeriodicalIF\":3.0000,\"publicationDate\":\"2025-05-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Materialia\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2589152925001206\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MATERIALS SCIENCE, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Materialia","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2589152925001206","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
Macrophage-mediated control of implant-associated biofilms in a three-dimensional human oral mucosa model
Macrophages are pivotal in regulating inflammation and facilitating pathogen clearance, particularly in peri-implant environments prone to biofilm infections. For a better understanding of the role of these immune cells in host-biofilm-implant interactions, we developed a complex three-dimensional (3D) implant-tissue-oral-bacterial-biofilm model (INTERbACT) with integrated macrophages to mimic the intricate triangular interactions between implant materials, biofilms, and the host, in conditions simulating the in vivo environment. The INTERbACT model includes a peri-implant mucosa with collagen-embedded fibroblasts and macrophages, overlaid with a multi-layered oral epithelium, as well as a multi-species biofilm. Histological analysis demonstrated a preserved peri-implant architecture with high cell viability. Co-cultivation with multi-species biofilms provided valuable insights into macrophage roles in pathogen defence and inflammation regulation. In tissues lacking macrophages, biofilm exposure led to compromised epithelial integrity, whereas macrophage-containing tissues maintained their epithelial structure. Macrophages significantly reduced the biofilm biomass while promoting bacterial death. Inflammatory cytokine levels elevated under sterile conditions decreased upon biofilm exposure, suggesting a biofilm-mediated immune suppression. Cytokine expression levels differentially reacted to biofilm exposure and macrophage concentration, with IL-1β and IL-17 levels notably elevated in biofilm-exposed tissues, aligning with clinical observations of peri-implant inflammation. Our findings demonstrate that the INTERbACT model, after incorporation of macrophages, serves as a physiologically relevant platform for studying host-pathogen dynamics and allows to identify key inflammatory markers associated with biofilm-related complications. Furthermore, this model holds significant potential for evaluating novel therapeutic strategies, such as sensor-actuator systems to detect and combat pathogenic biofilms, improving clinical outcomes in peri-implantitis management.
期刊介绍:
Materialia is a multidisciplinary journal of materials science and engineering that publishes original peer-reviewed research articles. Articles in Materialia advance the understanding of the relationship between processing, structure, property, and function of materials.
Materialia publishes full-length research articles, review articles, and letters (short communications). In addition to receiving direct submissions, Materialia also accepts transfers from Acta Materialia, Inc. partner journals. Materialia offers authors the choice to publish on an open access model (with author fee), or on a subscription model (with no author fee).