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Gut bacteria signaling to mitochondria in intestinal inflammation and cancer

The gastrointestinal microbiome plays a pivotal role in physiological homeostasis of the intestine as well as in the pathophysiology of diseases including inflammatory bowel diseases (IBD) and colorectal cancer (CRC). Emerging evidence suggests that gut microbiota signal to the mitochondria of mucos...

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Detalles Bibliográficos
Autores principales: Jackson, Dakota N., Theiss, Arianne L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7524274/
https://www.ncbi.nlm.nih.gov/pubmed/30913966
http://dx.doi.org/10.1080/19490976.2019.1592421
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author Jackson, Dakota N.
Theiss, Arianne L.
author_facet Jackson, Dakota N.
Theiss, Arianne L.
author_sort Jackson, Dakota N.
collection PubMed
description The gastrointestinal microbiome plays a pivotal role in physiological homeostasis of the intestine as well as in the pathophysiology of diseases including inflammatory bowel diseases (IBD) and colorectal cancer (CRC). Emerging evidence suggests that gut microbiota signal to the mitochondria of mucosal cells, including epithelial cells and immune cells. Gut microbiota signaling to mitochondria has been shown to alter mitochondrial metabolism, activate immune cells, induce inflammasome signaling, and alter epithelial barrier function. Both dysbiosis of the gut microbiota and mitochondrial dysfunction are associated with chronic intestinal inflammation and CRC. This review discusses mitochondrial metabolism of gut mucosal cells, mitochondrial dysfunction, and known gut microbiota-mediated mitochondrial alterations during IBD and CRC.
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spelling pubmed-75242742020-10-06 Gut bacteria signaling to mitochondria in intestinal inflammation and cancer Jackson, Dakota N. Theiss, Arianne L. Gut Microbes Review The gastrointestinal microbiome plays a pivotal role in physiological homeostasis of the intestine as well as in the pathophysiology of diseases including inflammatory bowel diseases (IBD) and colorectal cancer (CRC). Emerging evidence suggests that gut microbiota signal to the mitochondria of mucosal cells, including epithelial cells and immune cells. Gut microbiota signaling to mitochondria has been shown to alter mitochondrial metabolism, activate immune cells, induce inflammasome signaling, and alter epithelial barrier function. Both dysbiosis of the gut microbiota and mitochondrial dysfunction are associated with chronic intestinal inflammation and CRC. This review discusses mitochondrial metabolism of gut mucosal cells, mitochondrial dysfunction, and known gut microbiota-mediated mitochondrial alterations during IBD and CRC. Taylor & Francis 2019-03-26 /pmc/articles/PMC7524274/ /pubmed/30913966 http://dx.doi.org/10.1080/19490976.2019.1592421 Text en © 2019 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.
spellingShingle Review
Jackson, Dakota N.
Theiss, Arianne L.
Gut bacteria signaling to mitochondria in intestinal inflammation and cancer
title Gut bacteria signaling to mitochondria in intestinal inflammation and cancer
title_full Gut bacteria signaling to mitochondria in intestinal inflammation and cancer
title_fullStr Gut bacteria signaling to mitochondria in intestinal inflammation and cancer
title_full_unstemmed Gut bacteria signaling to mitochondria in intestinal inflammation and cancer
title_short Gut bacteria signaling to mitochondria in intestinal inflammation and cancer
title_sort gut bacteria signaling to mitochondria in intestinal inflammation and cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7524274/
https://www.ncbi.nlm.nih.gov/pubmed/30913966
http://dx.doi.org/10.1080/19490976.2019.1592421
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