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Consequences of collagen induced inflammatory arthritis on circadian regulation of the gut microbiome
The gut microbiota is important for host health and immune system function. Moreover autoimmune diseases, such as rheumatoid arthritis, are associated with significant gut microbiota dysbiosis, although the causes and consequences of this are not fully understood. It has become clear that the compos...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10107696/ https://www.ncbi.nlm.nih.gov/pubmed/36520064 http://dx.doi.org/10.1096/fj.202201728R |
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author | Simpkins, Devin Amanda Downton, Polly Gray, Kathryn J. Dickson, Suzanna H. Maidstone, Robert J. Konkel, Joanne E. Hepworth, Matthew R. Ray, David W. Bechtold, David A. Gibbs, Julie Elizabeth |
author_facet | Simpkins, Devin Amanda Downton, Polly Gray, Kathryn J. Dickson, Suzanna H. Maidstone, Robert J. Konkel, Joanne E. Hepworth, Matthew R. Ray, David W. Bechtold, David A. Gibbs, Julie Elizabeth |
author_sort | Simpkins, Devin Amanda |
collection | PubMed |
description | The gut microbiota is important for host health and immune system function. Moreover autoimmune diseases, such as rheumatoid arthritis, are associated with significant gut microbiota dysbiosis, although the causes and consequences of this are not fully understood. It has become clear that the composition and metabolic outputs of the microbiome exhibit robust 24 h oscillations, a result of daily variation in timing of food intake as well as rhythmic circadian clock function in the gut. Here, we report that experimental inflammatory arthritis leads to a re‐organization of circadian rhythmicity in both the gut and associated microbiome. Mice with collagen induced arthritis exhibited extensive changes in rhythmic gene expression in the colon, and reduced barrier integrity. Re‐modeling of the host gut circadian transcriptome was accompanied by significant alteration of the microbiota, including widespread loss of rhythmicity in symbiont species of Lactobacillus, and alteration in circulating microbial derived factors, such as tryptophan metabolites, which are associated with maintenance of barrier function and immune cell populations within the gut. These findings highlight that altered circadian rhythmicity during inflammatory disease contributes to dysregulation of gut integrity and microbiome function. |
format | Online Article Text |
id | pubmed-10107696 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101076962023-04-18 Consequences of collagen induced inflammatory arthritis on circadian regulation of the gut microbiome Simpkins, Devin Amanda Downton, Polly Gray, Kathryn J. Dickson, Suzanna H. Maidstone, Robert J. Konkel, Joanne E. Hepworth, Matthew R. Ray, David W. Bechtold, David A. Gibbs, Julie Elizabeth FASEB J Research Articles The gut microbiota is important for host health and immune system function. Moreover autoimmune diseases, such as rheumatoid arthritis, are associated with significant gut microbiota dysbiosis, although the causes and consequences of this are not fully understood. It has become clear that the composition and metabolic outputs of the microbiome exhibit robust 24 h oscillations, a result of daily variation in timing of food intake as well as rhythmic circadian clock function in the gut. Here, we report that experimental inflammatory arthritis leads to a re‐organization of circadian rhythmicity in both the gut and associated microbiome. Mice with collagen induced arthritis exhibited extensive changes in rhythmic gene expression in the colon, and reduced barrier integrity. Re‐modeling of the host gut circadian transcriptome was accompanied by significant alteration of the microbiota, including widespread loss of rhythmicity in symbiont species of Lactobacillus, and alteration in circulating microbial derived factors, such as tryptophan metabolites, which are associated with maintenance of barrier function and immune cell populations within the gut. These findings highlight that altered circadian rhythmicity during inflammatory disease contributes to dysregulation of gut integrity and microbiome function. John Wiley and Sons Inc. 2022-12-15 2023-01 /pmc/articles/PMC10107696/ /pubmed/36520064 http://dx.doi.org/10.1096/fj.202201728R Text en © 2022 The Authors. The FASEB Journal published by Wiley Periodicals LLC on behalf of Federation of American Societies for Experimental Biology. 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 Simpkins, Devin Amanda Downton, Polly Gray, Kathryn J. Dickson, Suzanna H. Maidstone, Robert J. Konkel, Joanne E. Hepworth, Matthew R. Ray, David W. Bechtold, David A. Gibbs, Julie Elizabeth Consequences of collagen induced inflammatory arthritis on circadian regulation of the gut microbiome |
title | Consequences of collagen induced inflammatory arthritis on circadian regulation of the gut microbiome |
title_full | Consequences of collagen induced inflammatory arthritis on circadian regulation of the gut microbiome |
title_fullStr | Consequences of collagen induced inflammatory arthritis on circadian regulation of the gut microbiome |
title_full_unstemmed | Consequences of collagen induced inflammatory arthritis on circadian regulation of the gut microbiome |
title_short | Consequences of collagen induced inflammatory arthritis on circadian regulation of the gut microbiome |
title_sort | consequences of collagen induced inflammatory arthritis on circadian regulation of the gut microbiome |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10107696/ https://www.ncbi.nlm.nih.gov/pubmed/36520064 http://dx.doi.org/10.1096/fj.202201728R |
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