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Brown adipose tissue is the key depot for glucose clearance in microbiota depleted mice
Gut microbiota deficient mice demonstrate accelerated glucose clearance. However, which tissues are responsible for the upregulated glucose uptake remains unresolved, with different studies suggesting that browning of white adipose tissue, or modulated hepatic gluconeogenesis, may be related to enha...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8342435/ https://www.ncbi.nlm.nih.gov/pubmed/34354051 http://dx.doi.org/10.1038/s41467-021-24659-8 |
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author | Li, Min Li, Li Li, Baoguo Hambly, Catherine Wang, Guanlin Wu, Yingga Jin, Zengguang Wang, Anyongqi Niu, Chaoqun Wolfrum, Christian Speakman, John R. |
author_facet | Li, Min Li, Li Li, Baoguo Hambly, Catherine Wang, Guanlin Wu, Yingga Jin, Zengguang Wang, Anyongqi Niu, Chaoqun Wolfrum, Christian Speakman, John R. |
author_sort | Li, Min |
collection | PubMed |
description | Gut microbiota deficient mice demonstrate accelerated glucose clearance. However, which tissues are responsible for the upregulated glucose uptake remains unresolved, with different studies suggesting that browning of white adipose tissue, or modulated hepatic gluconeogenesis, may be related to enhanced glucose clearance when the gut microbiota is absent. Here, we investigate glucose uptake in 22 different tissues in 3 different mouse models. We find that gut microbiota depletion via treatment with antibiotic cocktails (ABX) promotes glucose uptake in brown adipose tissue (BAT) and cecum. Nevertheless, the adaptive thermogenesis and the expression of uncoupling protein 1 (UCP1) are dispensable for the increased glucose uptake and clearance. Deletion of Ucp1 expressing cells blunts the improvement of glucose clearance in ABX-treated mice. Our results indicate that BAT and cecum, but not white adipose tissue (WAT) or liver, contribute to the glucose uptake in the gut microbiota depleted mouse model and this response is dissociated from adaptive thermogenesis. |
format | Online Article Text |
id | pubmed-8342435 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-83424352021-08-20 Brown adipose tissue is the key depot for glucose clearance in microbiota depleted mice Li, Min Li, Li Li, Baoguo Hambly, Catherine Wang, Guanlin Wu, Yingga Jin, Zengguang Wang, Anyongqi Niu, Chaoqun Wolfrum, Christian Speakman, John R. Nat Commun Article Gut microbiota deficient mice demonstrate accelerated glucose clearance. However, which tissues are responsible for the upregulated glucose uptake remains unresolved, with different studies suggesting that browning of white adipose tissue, or modulated hepatic gluconeogenesis, may be related to enhanced glucose clearance when the gut microbiota is absent. Here, we investigate glucose uptake in 22 different tissues in 3 different mouse models. We find that gut microbiota depletion via treatment with antibiotic cocktails (ABX) promotes glucose uptake in brown adipose tissue (BAT) and cecum. Nevertheless, the adaptive thermogenesis and the expression of uncoupling protein 1 (UCP1) are dispensable for the increased glucose uptake and clearance. Deletion of Ucp1 expressing cells blunts the improvement of glucose clearance in ABX-treated mice. Our results indicate that BAT and cecum, but not white adipose tissue (WAT) or liver, contribute to the glucose uptake in the gut microbiota depleted mouse model and this response is dissociated from adaptive thermogenesis. Nature Publishing Group UK 2021-08-05 /pmc/articles/PMC8342435/ /pubmed/34354051 http://dx.doi.org/10.1038/s41467-021-24659-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Li, Min Li, Li Li, Baoguo Hambly, Catherine Wang, Guanlin Wu, Yingga Jin, Zengguang Wang, Anyongqi Niu, Chaoqun Wolfrum, Christian Speakman, John R. Brown adipose tissue is the key depot for glucose clearance in microbiota depleted mice |
title | Brown adipose tissue is the key depot for glucose clearance in microbiota depleted mice |
title_full | Brown adipose tissue is the key depot for glucose clearance in microbiota depleted mice |
title_fullStr | Brown adipose tissue is the key depot for glucose clearance in microbiota depleted mice |
title_full_unstemmed | Brown adipose tissue is the key depot for glucose clearance in microbiota depleted mice |
title_short | Brown adipose tissue is the key depot for glucose clearance in microbiota depleted mice |
title_sort | brown adipose tissue is the key depot for glucose clearance in microbiota depleted mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8342435/ https://www.ncbi.nlm.nih.gov/pubmed/34354051 http://dx.doi.org/10.1038/s41467-021-24659-8 |
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