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Industrialized human gut microbiota increases CD8+ T cells and mucus thickness in humanized mouse gut
Immigration to a highly industrialized nation has been associated with metabolic disease and simultaneous shifts in microbiota composition, but the underlying mechanisms are challenging to test in human studies. Here, we conducted a pilot study to assess the differential effects of human gut microbi...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10588527/ https://www.ncbi.nlm.nih.gov/pubmed/37853762 http://dx.doi.org/10.1080/19490976.2023.2266627 |
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author | Vangay, Pajau Ward, Tonya Lucas, Sarah Beura, Lalit K. Sabas, Dominique Abramson, Max Till, Lisa Hoops, Susan L. Kashyap, Purna Hunter, Ryan C. Masopust, David Knights, Dan |
author_facet | Vangay, Pajau Ward, Tonya Lucas, Sarah Beura, Lalit K. Sabas, Dominique Abramson, Max Till, Lisa Hoops, Susan L. Kashyap, Purna Hunter, Ryan C. Masopust, David Knights, Dan |
author_sort | Vangay, Pajau |
collection | PubMed |
description | Immigration to a highly industrialized nation has been associated with metabolic disease and simultaneous shifts in microbiota composition, but the underlying mechanisms are challenging to test in human studies. Here, we conducted a pilot study to assess the differential effects of human gut microbiota collected from the United States (US) and rural Thailand on the murine gut mucosa and immune system. Colonization of germ-free mice with microbiota from US individuals resulted in an increased accumulation of innate-like CD8 T cells in the small intestine lamina propria and intra-epithelial compartments when compared to colonization with microbiota from Thai individuals. Both TCRγδ and CD8αα T cells showed a marked increase in mice receiving Western microbiota and, interestingly, this phenotype was also associated with an increase in intestinal mucus thickness. Serendipitously, an accidentally infected group of mice corroborated this association between elevated inflammatory response and increased mucus thickness. These results suggest that Western-associated human gut microbes contribute to a pro-inflammatory immune response. |
format | Online Article Text |
id | pubmed-10588527 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-105885272023-10-21 Industrialized human gut microbiota increases CD8+ T cells and mucus thickness in humanized mouse gut Vangay, Pajau Ward, Tonya Lucas, Sarah Beura, Lalit K. Sabas, Dominique Abramson, Max Till, Lisa Hoops, Susan L. Kashyap, Purna Hunter, Ryan C. Masopust, David Knights, Dan Gut Microbes Brief Report Immigration to a highly industrialized nation has been associated with metabolic disease and simultaneous shifts in microbiota composition, but the underlying mechanisms are challenging to test in human studies. Here, we conducted a pilot study to assess the differential effects of human gut microbiota collected from the United States (US) and rural Thailand on the murine gut mucosa and immune system. Colonization of germ-free mice with microbiota from US individuals resulted in an increased accumulation of innate-like CD8 T cells in the small intestine lamina propria and intra-epithelial compartments when compared to colonization with microbiota from Thai individuals. Both TCRγδ and CD8αα T cells showed a marked increase in mice receiving Western microbiota and, interestingly, this phenotype was also associated with an increase in intestinal mucus thickness. Serendipitously, an accidentally infected group of mice corroborated this association between elevated inflammatory response and increased mucus thickness. These results suggest that Western-associated human gut microbes contribute to a pro-inflammatory immune response. Taylor & Francis 2023-10-18 /pmc/articles/PMC10588527/ /pubmed/37853762 http://dx.doi.org/10.1080/19490976.2023.2266627 Text en © 2023 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent. |
spellingShingle | Brief Report Vangay, Pajau Ward, Tonya Lucas, Sarah Beura, Lalit K. Sabas, Dominique Abramson, Max Till, Lisa Hoops, Susan L. Kashyap, Purna Hunter, Ryan C. Masopust, David Knights, Dan Industrialized human gut microbiota increases CD8+ T cells and mucus thickness in humanized mouse gut |
title | Industrialized human gut microbiota increases CD8+ T cells and mucus thickness in humanized mouse gut |
title_full | Industrialized human gut microbiota increases CD8+ T cells and mucus thickness in humanized mouse gut |
title_fullStr | Industrialized human gut microbiota increases CD8+ T cells and mucus thickness in humanized mouse gut |
title_full_unstemmed | Industrialized human gut microbiota increases CD8+ T cells and mucus thickness in humanized mouse gut |
title_short | Industrialized human gut microbiota increases CD8+ T cells and mucus thickness in humanized mouse gut |
title_sort | industrialized human gut microbiota increases cd8+ t cells and mucus thickness in humanized mouse gut |
topic | Brief Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10588527/ https://www.ncbi.nlm.nih.gov/pubmed/37853762 http://dx.doi.org/10.1080/19490976.2023.2266627 |
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