Cargando…
Intestinal microbiota shapes gut physiology and regulates enteric neurons and glia
BACKGROUND: The intestinal microbiota plays an important role in regulating gastrointestinal (GI) physiology in part through interactions with the enteric nervous system (ENS). Alterations in the gut microbiome frequently occur together with disturbances in enteric neural control in pathophysiologic...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8549243/ https://www.ncbi.nlm.nih.gov/pubmed/34702353 http://dx.doi.org/10.1186/s40168-021-01165-z |
_version_ | 1784590745129189376 |
---|---|
author | Vicentini, Fernando A. Keenan, Catherine M. Wallace, Laurie E. Woods, Crystal Cavin, Jean-Baptiste Flockton, Amanda R. Macklin, Wendy B. Belkind-Gerson, Jaime Hirota, Simon A. Sharkey, Keith A. |
author_facet | Vicentini, Fernando A. Keenan, Catherine M. Wallace, Laurie E. Woods, Crystal Cavin, Jean-Baptiste Flockton, Amanda R. Macklin, Wendy B. Belkind-Gerson, Jaime Hirota, Simon A. Sharkey, Keith A. |
author_sort | Vicentini, Fernando A. |
collection | PubMed |
description | BACKGROUND: The intestinal microbiota plays an important role in regulating gastrointestinal (GI) physiology in part through interactions with the enteric nervous system (ENS). Alterations in the gut microbiome frequently occur together with disturbances in enteric neural control in pathophysiological conditions. However, the mechanisms by which the microbiota regulates GI function and the structure of the ENS are incompletely understood. Using a mouse model of antibiotic (Abx)-induced bacterial depletion, we sought to determine the molecular mechanisms of microbial regulation of intestinal function and the integrity of the ENS. Spontaneous reconstitution of the Abx-depleted microbiota was used to assess the plasticity of structure and function of the GI tract and ENS. Microbiota-dependent molecular mechanisms of ENS neuronal survival and neurogenesis were also assessed. RESULTS: Adult male and female Abx-treated mice exhibited alterations in GI structure and function, including a longer small intestine, slower transit time, increased carbachol-stimulated ion secretion, and increased intestinal permeability. These alterations were accompanied by the loss of enteric neurons in the ileum and proximal colon in both submucosal and myenteric plexuses. A reduction in the number of enteric glia was only observed in the ileal myenteric plexus. Recovery of the microbiota restored intestinal function and stimulated enteric neurogenesis leading to increases in the number of enteric glia and neurons. Lipopolysaccharide (LPS) supplementation enhanced neuronal survival alongside bacterial depletion, but had no effect on neuronal recovery once the Abx-induced neuronal loss was established. In contrast, short-chain fatty acids (SCFA) were able to restore neuronal numbers after Abx-induced neuronal loss, demonstrating that SCFA stimulate enteric neurogenesis in vivo. CONCLUSIONS: Our results demonstrate a role for the gut microbiota in regulating the structure and function of the GI tract in a sex-independent manner. Moreover, the microbiota is essential for the maintenance of ENS integrity, by regulating enteric neuronal survival and promoting neurogenesis. Molecular determinants of the microbiota, LPS and SCFA, regulate enteric neuronal survival, while SCFA also stimulates neurogenesis. Our data reveal new insights into the role of the gut microbiota that could lead to therapeutic developments for the treatment of enteric neuropathies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-021-01165-z. |
format | Online Article Text |
id | pubmed-8549243 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-85492432021-10-27 Intestinal microbiota shapes gut physiology and regulates enteric neurons and glia Vicentini, Fernando A. Keenan, Catherine M. Wallace, Laurie E. Woods, Crystal Cavin, Jean-Baptiste Flockton, Amanda R. Macklin, Wendy B. Belkind-Gerson, Jaime Hirota, Simon A. Sharkey, Keith A. Microbiome Research BACKGROUND: The intestinal microbiota plays an important role in regulating gastrointestinal (GI) physiology in part through interactions with the enteric nervous system (ENS). Alterations in the gut microbiome frequently occur together with disturbances in enteric neural control in pathophysiological conditions. However, the mechanisms by which the microbiota regulates GI function and the structure of the ENS are incompletely understood. Using a mouse model of antibiotic (Abx)-induced bacterial depletion, we sought to determine the molecular mechanisms of microbial regulation of intestinal function and the integrity of the ENS. Spontaneous reconstitution of the Abx-depleted microbiota was used to assess the plasticity of structure and function of the GI tract and ENS. Microbiota-dependent molecular mechanisms of ENS neuronal survival and neurogenesis were also assessed. RESULTS: Adult male and female Abx-treated mice exhibited alterations in GI structure and function, including a longer small intestine, slower transit time, increased carbachol-stimulated ion secretion, and increased intestinal permeability. These alterations were accompanied by the loss of enteric neurons in the ileum and proximal colon in both submucosal and myenteric plexuses. A reduction in the number of enteric glia was only observed in the ileal myenteric plexus. Recovery of the microbiota restored intestinal function and stimulated enteric neurogenesis leading to increases in the number of enteric glia and neurons. Lipopolysaccharide (LPS) supplementation enhanced neuronal survival alongside bacterial depletion, but had no effect on neuronal recovery once the Abx-induced neuronal loss was established. In contrast, short-chain fatty acids (SCFA) were able to restore neuronal numbers after Abx-induced neuronal loss, demonstrating that SCFA stimulate enteric neurogenesis in vivo. CONCLUSIONS: Our results demonstrate a role for the gut microbiota in regulating the structure and function of the GI tract in a sex-independent manner. Moreover, the microbiota is essential for the maintenance of ENS integrity, by regulating enteric neuronal survival and promoting neurogenesis. Molecular determinants of the microbiota, LPS and SCFA, regulate enteric neuronal survival, while SCFA also stimulates neurogenesis. Our data reveal new insights into the role of the gut microbiota that could lead to therapeutic developments for the treatment of enteric neuropathies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-021-01165-z. BioMed Central 2021-10-26 /pmc/articles/PMC8549243/ /pubmed/34702353 http://dx.doi.org/10.1186/s40168-021-01165-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Vicentini, Fernando A. Keenan, Catherine M. Wallace, Laurie E. Woods, Crystal Cavin, Jean-Baptiste Flockton, Amanda R. Macklin, Wendy B. Belkind-Gerson, Jaime Hirota, Simon A. Sharkey, Keith A. Intestinal microbiota shapes gut physiology and regulates enteric neurons and glia |
title | Intestinal microbiota shapes gut physiology and regulates enteric neurons and glia |
title_full | Intestinal microbiota shapes gut physiology and regulates enteric neurons and glia |
title_fullStr | Intestinal microbiota shapes gut physiology and regulates enteric neurons and glia |
title_full_unstemmed | Intestinal microbiota shapes gut physiology and regulates enteric neurons and glia |
title_short | Intestinal microbiota shapes gut physiology and regulates enteric neurons and glia |
title_sort | intestinal microbiota shapes gut physiology and regulates enteric neurons and glia |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8549243/ https://www.ncbi.nlm.nih.gov/pubmed/34702353 http://dx.doi.org/10.1186/s40168-021-01165-z |
work_keys_str_mv | AT vicentinifernandoa intestinalmicrobiotashapesgutphysiologyandregulatesentericneuronsandglia AT keenancatherinem intestinalmicrobiotashapesgutphysiologyandregulatesentericneuronsandglia AT wallacelauriee intestinalmicrobiotashapesgutphysiologyandregulatesentericneuronsandglia AT woodscrystal intestinalmicrobiotashapesgutphysiologyandregulatesentericneuronsandglia AT cavinjeanbaptiste intestinalmicrobiotashapesgutphysiologyandregulatesentericneuronsandglia AT flocktonamandar intestinalmicrobiotashapesgutphysiologyandregulatesentericneuronsandglia AT macklinwendyb intestinalmicrobiotashapesgutphysiologyandregulatesentericneuronsandglia AT belkindgersonjaime intestinalmicrobiotashapesgutphysiologyandregulatesentericneuronsandglia AT hirotasimona intestinalmicrobiotashapesgutphysiologyandregulatesentericneuronsandglia AT sharkeykeitha intestinalmicrobiotashapesgutphysiologyandregulatesentericneuronsandglia |