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A microfluidics-based in vitro model of the gastrointestinal human–microbe interface

Changes in the human gastrointestinal microbiome are associated with several diseases. To infer causality, experiments in representative models are essential, but widely used animal models exhibit limitations. Here we present a modular, microfluidics-based model (HuMiX, human–microbial crosstalk), w...

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Autores principales: Shah, Pranjul, Fritz, Joëlle V., Glaab, Enrico, Desai, Mahesh S., Greenhalgh, Kacy, Frachet, Audrey, Niegowska, Magdalena, Estes, Matthew, Jäger, Christian, Seguin-Devaux, Carole, Zenhausern, Frederic, Wilmes, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4865890/
https://www.ncbi.nlm.nih.gov/pubmed/27168102
http://dx.doi.org/10.1038/ncomms11535
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author Shah, Pranjul
Fritz, Joëlle V.
Glaab, Enrico
Desai, Mahesh S.
Greenhalgh, Kacy
Frachet, Audrey
Niegowska, Magdalena
Estes, Matthew
Jäger, Christian
Seguin-Devaux, Carole
Zenhausern, Frederic
Wilmes, Paul
author_facet Shah, Pranjul
Fritz, Joëlle V.
Glaab, Enrico
Desai, Mahesh S.
Greenhalgh, Kacy
Frachet, Audrey
Niegowska, Magdalena
Estes, Matthew
Jäger, Christian
Seguin-Devaux, Carole
Zenhausern, Frederic
Wilmes, Paul
author_sort Shah, Pranjul
collection PubMed
description Changes in the human gastrointestinal microbiome are associated with several diseases. To infer causality, experiments in representative models are essential, but widely used animal models exhibit limitations. Here we present a modular, microfluidics-based model (HuMiX, human–microbial crosstalk), which allows co-culture of human and microbial cells under conditions representative of the gastrointestinal human–microbe interface. We demonstrate the ability of HuMiX to recapitulate in vivo transcriptional, metabolic and immunological responses in human intestinal epithelial cells following their co-culture with the commensal Lactobacillus rhamnosus GG (LGG) grown under anaerobic conditions. In addition, we show that the co-culture of human epithelial cells with the obligate anaerobe Bacteroides caccae and LGG results in a transcriptional response, which is distinct from that of a co-culture solely comprising LGG. HuMiX facilitates investigations of host–microbe molecular interactions and provides insights into a range of fundamental research questions linking the gastrointestinal microbiome to human health and disease.
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spelling pubmed-48658902016-05-24 A microfluidics-based in vitro model of the gastrointestinal human–microbe interface Shah, Pranjul Fritz, Joëlle V. Glaab, Enrico Desai, Mahesh S. Greenhalgh, Kacy Frachet, Audrey Niegowska, Magdalena Estes, Matthew Jäger, Christian Seguin-Devaux, Carole Zenhausern, Frederic Wilmes, Paul Nat Commun Article Changes in the human gastrointestinal microbiome are associated with several diseases. To infer causality, experiments in representative models are essential, but widely used animal models exhibit limitations. Here we present a modular, microfluidics-based model (HuMiX, human–microbial crosstalk), which allows co-culture of human and microbial cells under conditions representative of the gastrointestinal human–microbe interface. We demonstrate the ability of HuMiX to recapitulate in vivo transcriptional, metabolic and immunological responses in human intestinal epithelial cells following their co-culture with the commensal Lactobacillus rhamnosus GG (LGG) grown under anaerobic conditions. In addition, we show that the co-culture of human epithelial cells with the obligate anaerobe Bacteroides caccae and LGG results in a transcriptional response, which is distinct from that of a co-culture solely comprising LGG. HuMiX facilitates investigations of host–microbe molecular interactions and provides insights into a range of fundamental research questions linking the gastrointestinal microbiome to human health and disease. Nature Publishing Group 2016-05-11 /pmc/articles/PMC4865890/ /pubmed/27168102 http://dx.doi.org/10.1038/ncomms11535 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Shah, Pranjul
Fritz, Joëlle V.
Glaab, Enrico
Desai, Mahesh S.
Greenhalgh, Kacy
Frachet, Audrey
Niegowska, Magdalena
Estes, Matthew
Jäger, Christian
Seguin-Devaux, Carole
Zenhausern, Frederic
Wilmes, Paul
A microfluidics-based in vitro model of the gastrointestinal human–microbe interface
title A microfluidics-based in vitro model of the gastrointestinal human–microbe interface
title_full A microfluidics-based in vitro model of the gastrointestinal human–microbe interface
title_fullStr A microfluidics-based in vitro model of the gastrointestinal human–microbe interface
title_full_unstemmed A microfluidics-based in vitro model of the gastrointestinal human–microbe interface
title_short A microfluidics-based in vitro model of the gastrointestinal human–microbe interface
title_sort microfluidics-based in vitro model of the gastrointestinal human–microbe interface
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4865890/
https://www.ncbi.nlm.nih.gov/pubmed/27168102
http://dx.doi.org/10.1038/ncomms11535
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