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A 3D Bioprinted Gut Anaerobic Model for Studying Bacteria–Host Interactions
The role of the human intestinal tract in host–microbe interactions has been highlighted in recent years. Several 3-dimensional (3D) models have been developed to reproduce the physiological characteristics of the human gut and to investigate the function of the gut microbiota. One challenge for 3D...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AAAS
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10076011/ https://www.ncbi.nlm.nih.gov/pubmed/37040488 http://dx.doi.org/10.34133/research.0058 |
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author | Cheng, Liqin Liu, Tingting Liu, Qiongg Lian, Liming Tang, Guosheng Mille, Luis Santiago García, Fabricio Romero Engstrand, Lars Zhang, Yu Shrike Du, Juan |
author_facet | Cheng, Liqin Liu, Tingting Liu, Qiongg Lian, Liming Tang, Guosheng Mille, Luis Santiago García, Fabricio Romero Engstrand, Lars Zhang, Yu Shrike Du, Juan |
author_sort | Cheng, Liqin |
collection | PubMed |
description | The role of the human intestinal tract in host–microbe interactions has been highlighted in recent years. Several 3-dimensional (3D) models have been developed to reproduce the physiological characteristics of the human gut and to investigate the function of the gut microbiota. One challenge for 3D models is to recapitulate the low oxygen concentrations in the intestinal lumen. Moreover, most earlier 3D culture systems used a membrane to physically separate bacteria from the intestinal epithelium, which has sometimes made the studies of bacteria adhering to or invading cells less feasible. We report the establishment of a 3D gut epithelium model and cultured it at high cell viability under an anaerobic condition. We further cocultured intestinal bacteria including both commensal and pathogen directly with epithelial cells in the established 3D model under the anaerobic condition. We subsequently compared the gene expression differences of aerobic and anaerobic conditions for cell and bacterial growth via dual RNA sequencing. Our study provides a physiologically relevant 3D gut epithelium model that mimics the anaerobic condition in the intestinal lumen and supplies a powerful system for future in-depth gut–microbe interactional investigations. |
format | Online Article Text |
id | pubmed-10076011 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | AAAS |
record_format | MEDLINE/PubMed |
spelling | pubmed-100760112023-04-06 A 3D Bioprinted Gut Anaerobic Model for Studying Bacteria–Host Interactions Cheng, Liqin Liu, Tingting Liu, Qiongg Lian, Liming Tang, Guosheng Mille, Luis Santiago García, Fabricio Romero Engstrand, Lars Zhang, Yu Shrike Du, Juan Research (Wash D C) Research Article The role of the human intestinal tract in host–microbe interactions has been highlighted in recent years. Several 3-dimensional (3D) models have been developed to reproduce the physiological characteristics of the human gut and to investigate the function of the gut microbiota. One challenge for 3D models is to recapitulate the low oxygen concentrations in the intestinal lumen. Moreover, most earlier 3D culture systems used a membrane to physically separate bacteria from the intestinal epithelium, which has sometimes made the studies of bacteria adhering to or invading cells less feasible. We report the establishment of a 3D gut epithelium model and cultured it at high cell viability under an anaerobic condition. We further cocultured intestinal bacteria including both commensal and pathogen directly with epithelial cells in the established 3D model under the anaerobic condition. We subsequently compared the gene expression differences of aerobic and anaerobic conditions for cell and bacterial growth via dual RNA sequencing. Our study provides a physiologically relevant 3D gut epithelium model that mimics the anaerobic condition in the intestinal lumen and supplies a powerful system for future in-depth gut–microbe interactional investigations. AAAS 2023-02-27 2023 /pmc/articles/PMC10076011/ /pubmed/37040488 http://dx.doi.org/10.34133/research.0058 Text en Copyright © 2023 Liqin Cheng et al. https://creativecommons.org/licenses/by/4.0/Exclusive licensee Science and Technology Review Publishing House. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY 4.0) (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Cheng, Liqin Liu, Tingting Liu, Qiongg Lian, Liming Tang, Guosheng Mille, Luis Santiago García, Fabricio Romero Engstrand, Lars Zhang, Yu Shrike Du, Juan A 3D Bioprinted Gut Anaerobic Model for Studying Bacteria–Host Interactions |
title | A 3D Bioprinted Gut Anaerobic Model for Studying Bacteria–Host Interactions |
title_full | A 3D Bioprinted Gut Anaerobic Model for Studying Bacteria–Host Interactions |
title_fullStr | A 3D Bioprinted Gut Anaerobic Model for Studying Bacteria–Host Interactions |
title_full_unstemmed | A 3D Bioprinted Gut Anaerobic Model for Studying Bacteria–Host Interactions |
title_short | A 3D Bioprinted Gut Anaerobic Model for Studying Bacteria–Host Interactions |
title_sort | 3d bioprinted gut anaerobic model for studying bacteria–host interactions |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10076011/ https://www.ncbi.nlm.nih.gov/pubmed/37040488 http://dx.doi.org/10.34133/research.0058 |
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