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Microbiota Modulates Cardiac Transcriptional Responses to Intermittent Hypoxia and Hypercapnia
The microbiota plays a critical role in regulating organismal health and response to environmental stresses. Intermittent hypoxia and hypercapnia, a condition that represents the main hallmark of obstructive sleep apnea in humans, is known to induce significant alterations in the gut microbiome and...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8267877/ https://www.ncbi.nlm.nih.gov/pubmed/34248668 http://dx.doi.org/10.3389/fphys.2021.680275 |
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author | Zhou, Dan Xue, Jin Miyamoto, Yukiko Poulsen, Orit Eckmann, Lars Haddad, Gabriel G. |
author_facet | Zhou, Dan Xue, Jin Miyamoto, Yukiko Poulsen, Orit Eckmann, Lars Haddad, Gabriel G. |
author_sort | Zhou, Dan |
collection | PubMed |
description | The microbiota plays a critical role in regulating organismal health and response to environmental stresses. Intermittent hypoxia and hypercapnia, a condition that represents the main hallmark of obstructive sleep apnea in humans, is known to induce significant alterations in the gut microbiome and metabolism, and promotes the progression of atherosclerosis in mouse models. To further understand the role of the microbiome in the cardiovascular response to intermittent hypoxia and hypercapnia, we developed a new rodent cage system that allows exposure of mice to controlled levels of O(2) and CO(2) under gnotobiotic conditions. Using this experimental setup, we determined the impact of the microbiome on the transcriptional response to intermittent hypoxia and hypercapnia in the left ventricle of the mouse heart. We identified significant changes in gene expression in both conventionally reared and germ-free mice. Following intermittent hypoxia and hypercapnia exposure, we detected 192 significant changes in conventionally reared mice (96 upregulated and 96 downregulated) and 161 significant changes (70 upregulated and 91 downregulated) in germ-free mice. Only 19 of these differentially expressed transcripts (∼10%) were common to conventionally reared and germ-free mice. Such distinct transcriptional responses imply that the host microbiota plays an important role in regulating the host transcriptional response to intermittent hypoxia and hypercapnia in the mouse heart. |
format | Online Article Text |
id | pubmed-8267877 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82678772021-07-10 Microbiota Modulates Cardiac Transcriptional Responses to Intermittent Hypoxia and Hypercapnia Zhou, Dan Xue, Jin Miyamoto, Yukiko Poulsen, Orit Eckmann, Lars Haddad, Gabriel G. Front Physiol Physiology The microbiota plays a critical role in regulating organismal health and response to environmental stresses. Intermittent hypoxia and hypercapnia, a condition that represents the main hallmark of obstructive sleep apnea in humans, is known to induce significant alterations in the gut microbiome and metabolism, and promotes the progression of atherosclerosis in mouse models. To further understand the role of the microbiome in the cardiovascular response to intermittent hypoxia and hypercapnia, we developed a new rodent cage system that allows exposure of mice to controlled levels of O(2) and CO(2) under gnotobiotic conditions. Using this experimental setup, we determined the impact of the microbiome on the transcriptional response to intermittent hypoxia and hypercapnia in the left ventricle of the mouse heart. We identified significant changes in gene expression in both conventionally reared and germ-free mice. Following intermittent hypoxia and hypercapnia exposure, we detected 192 significant changes in conventionally reared mice (96 upregulated and 96 downregulated) and 161 significant changes (70 upregulated and 91 downregulated) in germ-free mice. Only 19 of these differentially expressed transcripts (∼10%) were common to conventionally reared and germ-free mice. Such distinct transcriptional responses imply that the host microbiota plays an important role in regulating the host transcriptional response to intermittent hypoxia and hypercapnia in the mouse heart. Frontiers Media S.A. 2021-06-25 /pmc/articles/PMC8267877/ /pubmed/34248668 http://dx.doi.org/10.3389/fphys.2021.680275 Text en Copyright © 2021 Zhou, Xue, Miyamoto, Poulsen, Eckmann and Haddad. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Physiology Zhou, Dan Xue, Jin Miyamoto, Yukiko Poulsen, Orit Eckmann, Lars Haddad, Gabriel G. Microbiota Modulates Cardiac Transcriptional Responses to Intermittent Hypoxia and Hypercapnia |
title | Microbiota Modulates Cardiac Transcriptional Responses to Intermittent Hypoxia and Hypercapnia |
title_full | Microbiota Modulates Cardiac Transcriptional Responses to Intermittent Hypoxia and Hypercapnia |
title_fullStr | Microbiota Modulates Cardiac Transcriptional Responses to Intermittent Hypoxia and Hypercapnia |
title_full_unstemmed | Microbiota Modulates Cardiac Transcriptional Responses to Intermittent Hypoxia and Hypercapnia |
title_short | Microbiota Modulates Cardiac Transcriptional Responses to Intermittent Hypoxia and Hypercapnia |
title_sort | microbiota modulates cardiac transcriptional responses to intermittent hypoxia and hypercapnia |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8267877/ https://www.ncbi.nlm.nih.gov/pubmed/34248668 http://dx.doi.org/10.3389/fphys.2021.680275 |
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