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Advances in modelling the human microbiome–gut–brain axis in vitro
The human gut microbiome has emerged as a key player in the bidirectional communication of the gut–brain axis, affecting various aspects of homeostasis and pathophysiology. Until recently, the majority of studies that seek to explore the mechanisms underlying the microbiome–gut–brain axis cross-talk...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Portland Press Ltd.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7924999/ https://www.ncbi.nlm.nih.gov/pubmed/33544117 http://dx.doi.org/10.1042/BST20200338 |
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author | Moysidou, Chrysanthi-Maria Owens, Róisín M. |
author_facet | Moysidou, Chrysanthi-Maria Owens, Róisín M. |
author_sort | Moysidou, Chrysanthi-Maria |
collection | PubMed |
description | The human gut microbiome has emerged as a key player in the bidirectional communication of the gut–brain axis, affecting various aspects of homeostasis and pathophysiology. Until recently, the majority of studies that seek to explore the mechanisms underlying the microbiome–gut–brain axis cross-talk, relied almost exclusively on animal models, and particularly gnotobiotic mice. Despite the great progress made with these models, various limitations, including ethical considerations and interspecies differences that limit the translatability of data to human systems, pushed researchers to seek for alternatives. Over the past decades, the field of in vitro modelling of tissues has experienced tremendous growth, thanks to advances in 3D cell biology, materials, science and bioengineering, pushing further the borders of our ability to more faithfully emulate the in vivo situation. The discovery of stem cells has offered a new source of cells, while their use in generating gastrointestinal and brain organoids, among other tissues, has enabled the development of novel 3D tissues that better mimic the native tissue structure and function, compared with traditional assays. In parallel, organs-on-chips technology and bioengineered tissues have emerged as highly promising alternatives to animal models for a wide range of applications. Here, we discuss how recent advances and trends in this area can be applied in host–microbe and host–pathogen interaction studies. In addition, we highlight paradigm shifts in engineering more robust human microbiome-gut-brain axis models and their potential to expand our understanding of this complex system and hence explore novel, microbiome-based therapeutic approaches. |
format | Online Article Text |
id | pubmed-7924999 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Portland Press Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-79249992021-03-08 Advances in modelling the human microbiome–gut–brain axis in vitro Moysidou, Chrysanthi-Maria Owens, Róisín M. Biochem Soc Trans Review Articles The human gut microbiome has emerged as a key player in the bidirectional communication of the gut–brain axis, affecting various aspects of homeostasis and pathophysiology. Until recently, the majority of studies that seek to explore the mechanisms underlying the microbiome–gut–brain axis cross-talk, relied almost exclusively on animal models, and particularly gnotobiotic mice. Despite the great progress made with these models, various limitations, including ethical considerations and interspecies differences that limit the translatability of data to human systems, pushed researchers to seek for alternatives. Over the past decades, the field of in vitro modelling of tissues has experienced tremendous growth, thanks to advances in 3D cell biology, materials, science and bioengineering, pushing further the borders of our ability to more faithfully emulate the in vivo situation. The discovery of stem cells has offered a new source of cells, while their use in generating gastrointestinal and brain organoids, among other tissues, has enabled the development of novel 3D tissues that better mimic the native tissue structure and function, compared with traditional assays. In parallel, organs-on-chips technology and bioengineered tissues have emerged as highly promising alternatives to animal models for a wide range of applications. Here, we discuss how recent advances and trends in this area can be applied in host–microbe and host–pathogen interaction studies. In addition, we highlight paradigm shifts in engineering more robust human microbiome-gut-brain axis models and their potential to expand our understanding of this complex system and hence explore novel, microbiome-based therapeutic approaches. Portland Press Ltd. 2021-02-26 2021-02-05 /pmc/articles/PMC7924999/ /pubmed/33544117 http://dx.doi.org/10.1042/BST20200338 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by/4.0/ This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) . Open access for this article was enabled by the participation of University of Cambridge in an all-inclusive Read & Publish pilot with Portland Press and the Biochemical Society under a transformative agreement with JISC. |
spellingShingle | Review Articles Moysidou, Chrysanthi-Maria Owens, Róisín M. Advances in modelling the human microbiome–gut–brain axis in vitro |
title | Advances in modelling the human microbiome–gut–brain axis in vitro |
title_full | Advances in modelling the human microbiome–gut–brain axis in vitro |
title_fullStr | Advances in modelling the human microbiome–gut–brain axis in vitro |
title_full_unstemmed | Advances in modelling the human microbiome–gut–brain axis in vitro |
title_short | Advances in modelling the human microbiome–gut–brain axis in vitro |
title_sort | advances in modelling the human microbiome–gut–brain axis in vitro |
topic | Review Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7924999/ https://www.ncbi.nlm.nih.gov/pubmed/33544117 http://dx.doi.org/10.1042/BST20200338 |
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