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Immune Responses Regulated by Key Periodontal Bacteria in Germ-Free Mice

The immune dysregulation induced by periodontal bacteria has important roles in the development of periodontitis. However, the role of key periodontal bacteria in local and systemic immunity has not been comprehensively studied. Herein, to explore immunoregulation maps of key periodontal bacteria, a...

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Autores principales: Shen, Xin, Yang, Yutao, Li, Jian, Zhang, Bo, Wei, Wei, Lu, Changqing, Yan, Caixia, Wei, Hong, Li, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9146732/
https://www.ncbi.nlm.nih.gov/pubmed/35631034
http://dx.doi.org/10.3390/pathogens11050513
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author Shen, Xin
Yang, Yutao
Li, Jian
Zhang, Bo
Wei, Wei
Lu, Changqing
Yan, Caixia
Wei, Hong
Li, Yan
author_facet Shen, Xin
Yang, Yutao
Li, Jian
Zhang, Bo
Wei, Wei
Lu, Changqing
Yan, Caixia
Wei, Hong
Li, Yan
author_sort Shen, Xin
collection PubMed
description The immune dysregulation induced by periodontal bacteria has important roles in the development of periodontitis. However, the role of key periodontal bacteria in local and systemic immunity has not been comprehensively studied. Herein, to explore immunoregulation maps of key periodontal bacteria, a mono-colonized germ-free mice model with P. gingivalis, F. nucleatum, and T. denticola for two weeks was designed in this study. The alveolar bone loss was determined by micro-CT. A total of 14 types of innate and adaptive immune cells of the gingiva, spleen, and colon were detected by multi-color flow cytometry. P. gingivalis induced the strongest innate immune response in gingiva and mononuclear phagocytes (MNPs) changed most significantly, compared to F. nucleatum and T. denticola. Immune dysregulation of the colon was widely induced by F. nucleatum. T. denticola mainly induced immune disorder in spleen. ILC3s, Tregs, CD11B+ dendritic cells s, MNPs, macrophages, and plasmacytoid dendritic cells were the main types in response to key periodontal bacteria. However, the alveolar bone loss was not induced by key periodontal bacteria. In conclusion, the overall immunoregulation of monomicrobial stimuli to decipher the complexities of periodontitis was provided in this study. P. gingivalis, F. nucleatum, and T. denticola have different effects on local and systemic immunity in gingiva, colon, and spleen of germ-free mice.
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spelling pubmed-91467322022-05-29 Immune Responses Regulated by Key Periodontal Bacteria in Germ-Free Mice Shen, Xin Yang, Yutao Li, Jian Zhang, Bo Wei, Wei Lu, Changqing Yan, Caixia Wei, Hong Li, Yan Pathogens Article The immune dysregulation induced by periodontal bacteria has important roles in the development of periodontitis. However, the role of key periodontal bacteria in local and systemic immunity has not been comprehensively studied. Herein, to explore immunoregulation maps of key periodontal bacteria, a mono-colonized germ-free mice model with P. gingivalis, F. nucleatum, and T. denticola for two weeks was designed in this study. The alveolar bone loss was determined by micro-CT. A total of 14 types of innate and adaptive immune cells of the gingiva, spleen, and colon were detected by multi-color flow cytometry. P. gingivalis induced the strongest innate immune response in gingiva and mononuclear phagocytes (MNPs) changed most significantly, compared to F. nucleatum and T. denticola. Immune dysregulation of the colon was widely induced by F. nucleatum. T. denticola mainly induced immune disorder in spleen. ILC3s, Tregs, CD11B+ dendritic cells s, MNPs, macrophages, and plasmacytoid dendritic cells were the main types in response to key periodontal bacteria. However, the alveolar bone loss was not induced by key periodontal bacteria. In conclusion, the overall immunoregulation of monomicrobial stimuli to decipher the complexities of periodontitis was provided in this study. P. gingivalis, F. nucleatum, and T. denticola have different effects on local and systemic immunity in gingiva, colon, and spleen of germ-free mice. MDPI 2022-04-26 /pmc/articles/PMC9146732/ /pubmed/35631034 http://dx.doi.org/10.3390/pathogens11050513 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Shen, Xin
Yang, Yutao
Li, Jian
Zhang, Bo
Wei, Wei
Lu, Changqing
Yan, Caixia
Wei, Hong
Li, Yan
Immune Responses Regulated by Key Periodontal Bacteria in Germ-Free Mice
title Immune Responses Regulated by Key Periodontal Bacteria in Germ-Free Mice
title_full Immune Responses Regulated by Key Periodontal Bacteria in Germ-Free Mice
title_fullStr Immune Responses Regulated by Key Periodontal Bacteria in Germ-Free Mice
title_full_unstemmed Immune Responses Regulated by Key Periodontal Bacteria in Germ-Free Mice
title_short Immune Responses Regulated by Key Periodontal Bacteria in Germ-Free Mice
title_sort immune responses regulated by key periodontal bacteria in germ-free mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9146732/
https://www.ncbi.nlm.nih.gov/pubmed/35631034
http://dx.doi.org/10.3390/pathogens11050513
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