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Three‐Dimensional Humanized Model of the Periodontal Gingival Pocket to Study Oral Microbiome
The oral cavity contains distinct microenvironments that serve as oral barriers, such as the non‐shedding surface of the teeth (e.g., enamel), the epithelial mucosa and gingival tissue (attached gingiva) where microbial communities coexist. The interactions and balances between these communities are...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10131835/ https://www.ncbi.nlm.nih.gov/pubmed/36825685 http://dx.doi.org/10.1002/advs.202205473 |
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author | Adelfio, Miryam Martin‐Moldes, Zaira Erndt‐Marino, Joshua Tozzi, Lorenzo Duncan, Margaret J. Hasturk, Hatice Kaplan, David L. Ghezzi, Chiara E. |
author_facet | Adelfio, Miryam Martin‐Moldes, Zaira Erndt‐Marino, Joshua Tozzi, Lorenzo Duncan, Margaret J. Hasturk, Hatice Kaplan, David L. Ghezzi, Chiara E. |
author_sort | Adelfio, Miryam |
collection | PubMed |
description | The oral cavity contains distinct microenvironments that serve as oral barriers, such as the non‐shedding surface of the teeth (e.g., enamel), the epithelial mucosa and gingival tissue (attached gingiva) where microbial communities coexist. The interactions and balances between these communities are responsible for oral tissue homeostasis or dysbiosis, that ultimately dictate health or disease. Disruption of this equilibrium can lead to chronic inflammation and permanent tissue damage in the case of chronic periodontitis. There are currently no experimental tissue models able to mimic the structural, physical, and metabolic conditions present in the human oral gingival tissue to support the long‐term investigation of host–pathogens imbalances. Herein, the authors report an in vitro 3D anatomical gingival tissue model, fabricated from silk biopolymer by casting a replica mold of an adult human mandibular gingiva to recreate a tooth‐gum unit. The model is based on human primary cultures that recapitulate physiological tissue organization, as well as a native oxygen gradient within the gingival pocket to support human subgingival plaque microbiome with a physiologically relevant level of microbial diversity up to 24 h. The modulation of inflammatory markers in the presence of oral microbiome indicates the humanized functional response of this model and establishes a new set of tools to investigate host–pathogen imbalances in gingivitis and periodontal diseases. |
format | Online Article Text |
id | pubmed-10131835 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101318352023-04-27 Three‐Dimensional Humanized Model of the Periodontal Gingival Pocket to Study Oral Microbiome Adelfio, Miryam Martin‐Moldes, Zaira Erndt‐Marino, Joshua Tozzi, Lorenzo Duncan, Margaret J. Hasturk, Hatice Kaplan, David L. Ghezzi, Chiara E. Adv Sci (Weinh) Research Articles The oral cavity contains distinct microenvironments that serve as oral barriers, such as the non‐shedding surface of the teeth (e.g., enamel), the epithelial mucosa and gingival tissue (attached gingiva) where microbial communities coexist. The interactions and balances between these communities are responsible for oral tissue homeostasis or dysbiosis, that ultimately dictate health or disease. Disruption of this equilibrium can lead to chronic inflammation and permanent tissue damage in the case of chronic periodontitis. There are currently no experimental tissue models able to mimic the structural, physical, and metabolic conditions present in the human oral gingival tissue to support the long‐term investigation of host–pathogens imbalances. Herein, the authors report an in vitro 3D anatomical gingival tissue model, fabricated from silk biopolymer by casting a replica mold of an adult human mandibular gingiva to recreate a tooth‐gum unit. The model is based on human primary cultures that recapitulate physiological tissue organization, as well as a native oxygen gradient within the gingival pocket to support human subgingival plaque microbiome with a physiologically relevant level of microbial diversity up to 24 h. The modulation of inflammatory markers in the presence of oral microbiome indicates the humanized functional response of this model and establishes a new set of tools to investigate host–pathogen imbalances in gingivitis and periodontal diseases. John Wiley and Sons Inc. 2023-02-24 /pmc/articles/PMC10131835/ /pubmed/36825685 http://dx.doi.org/10.1002/advs.202205473 Text en © 2023 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Adelfio, Miryam Martin‐Moldes, Zaira Erndt‐Marino, Joshua Tozzi, Lorenzo Duncan, Margaret J. Hasturk, Hatice Kaplan, David L. Ghezzi, Chiara E. Three‐Dimensional Humanized Model of the Periodontal Gingival Pocket to Study Oral Microbiome |
title | Three‐Dimensional Humanized Model of the Periodontal Gingival Pocket to Study Oral Microbiome |
title_full | Three‐Dimensional Humanized Model of the Periodontal Gingival Pocket to Study Oral Microbiome |
title_fullStr | Three‐Dimensional Humanized Model of the Periodontal Gingival Pocket to Study Oral Microbiome |
title_full_unstemmed | Three‐Dimensional Humanized Model of the Periodontal Gingival Pocket to Study Oral Microbiome |
title_short | Three‐Dimensional Humanized Model of the Periodontal Gingival Pocket to Study Oral Microbiome |
title_sort | three‐dimensional humanized model of the periodontal gingival pocket to study oral microbiome |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10131835/ https://www.ncbi.nlm.nih.gov/pubmed/36825685 http://dx.doi.org/10.1002/advs.202205473 |
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