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Short-chain fatty acids regulate systemic bone mass and protect from pathological bone loss
Microbial metabolites are known to modulate immune responses of the host. The main metabolites derived from microbial fermentation of dietary fibers in the intestine, short-chain fatty acids (SCFA), affect local and systemic immune functions. Here we show that SCFA are regulators of osteoclast metab...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5754356/ https://www.ncbi.nlm.nih.gov/pubmed/29302038 http://dx.doi.org/10.1038/s41467-017-02490-4 |
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author | Lucas, Sébastien Omata, Yasunori Hofmann, Jörg Böttcher, Martin Iljazovic, Aida Sarter, Kerstin Albrecht, Olivia Schulz, Oscar Krishnacoumar, Brenda Krönke, Gerhard Herrmann, Martin Mougiakakos, Dimitrios Strowig, Till Schett, Georg Zaiss, Mario M. |
author_facet | Lucas, Sébastien Omata, Yasunori Hofmann, Jörg Böttcher, Martin Iljazovic, Aida Sarter, Kerstin Albrecht, Olivia Schulz, Oscar Krishnacoumar, Brenda Krönke, Gerhard Herrmann, Martin Mougiakakos, Dimitrios Strowig, Till Schett, Georg Zaiss, Mario M. |
author_sort | Lucas, Sébastien |
collection | PubMed |
description | Microbial metabolites are known to modulate immune responses of the host. The main metabolites derived from microbial fermentation of dietary fibers in the intestine, short-chain fatty acids (SCFA), affect local and systemic immune functions. Here we show that SCFA are regulators of osteoclast metabolism and bone mass in vivo. Treatment of mice with SCFA as well as feeding with a high-fiber diet significantly increases bone mass and prevents postmenopausal and inflammation-induced bone loss. The protective effects of SCFA on bone mass are associated with inhibition of osteoclast differentiation and bone resorption in vitro and in vivo, while bone formation is not affected. Mechanistically, propionate (C3) and butyrate (C4) induce metabolic reprogramming of osteoclasts resulting in enhanced glycolysis at the expense of oxidative phosphorylation, thereby downregulating essential osteoclast genes such as TRAF6 and NFATc1. In summary, these data identify SCFA as potent regulators of osteoclast metabolism and bone homeostasis. |
format | Online Article Text |
id | pubmed-5754356 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57543562018-01-12 Short-chain fatty acids regulate systemic bone mass and protect from pathological bone loss Lucas, Sébastien Omata, Yasunori Hofmann, Jörg Böttcher, Martin Iljazovic, Aida Sarter, Kerstin Albrecht, Olivia Schulz, Oscar Krishnacoumar, Brenda Krönke, Gerhard Herrmann, Martin Mougiakakos, Dimitrios Strowig, Till Schett, Georg Zaiss, Mario M. Nat Commun Article Microbial metabolites are known to modulate immune responses of the host. The main metabolites derived from microbial fermentation of dietary fibers in the intestine, short-chain fatty acids (SCFA), affect local and systemic immune functions. Here we show that SCFA are regulators of osteoclast metabolism and bone mass in vivo. Treatment of mice with SCFA as well as feeding with a high-fiber diet significantly increases bone mass and prevents postmenopausal and inflammation-induced bone loss. The protective effects of SCFA on bone mass are associated with inhibition of osteoclast differentiation and bone resorption in vitro and in vivo, while bone formation is not affected. Mechanistically, propionate (C3) and butyrate (C4) induce metabolic reprogramming of osteoclasts resulting in enhanced glycolysis at the expense of oxidative phosphorylation, thereby downregulating essential osteoclast genes such as TRAF6 and NFATc1. In summary, these data identify SCFA as potent regulators of osteoclast metabolism and bone homeostasis. Nature Publishing Group UK 2018-01-04 /pmc/articles/PMC5754356/ /pubmed/29302038 http://dx.doi.org/10.1038/s41467-017-02490-4 Text en © The Author(s) 2017 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/. |
spellingShingle | Article Lucas, Sébastien Omata, Yasunori Hofmann, Jörg Böttcher, Martin Iljazovic, Aida Sarter, Kerstin Albrecht, Olivia Schulz, Oscar Krishnacoumar, Brenda Krönke, Gerhard Herrmann, Martin Mougiakakos, Dimitrios Strowig, Till Schett, Georg Zaiss, Mario M. Short-chain fatty acids regulate systemic bone mass and protect from pathological bone loss |
title | Short-chain fatty acids regulate systemic bone mass and protect from pathological bone loss |
title_full | Short-chain fatty acids regulate systemic bone mass and protect from pathological bone loss |
title_fullStr | Short-chain fatty acids regulate systemic bone mass and protect from pathological bone loss |
title_full_unstemmed | Short-chain fatty acids regulate systemic bone mass and protect from pathological bone loss |
title_short | Short-chain fatty acids regulate systemic bone mass and protect from pathological bone loss |
title_sort | short-chain fatty acids regulate systemic bone mass and protect from pathological bone loss |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5754356/ https://www.ncbi.nlm.nih.gov/pubmed/29302038 http://dx.doi.org/10.1038/s41467-017-02490-4 |
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