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dc.contributor.authorLucas, Sébastien
dc.contributor.authorOmata, Yasunori
dc.contributor.authorHofmann, Jörg
dc.contributor.authorBöttcher, Martin
dc.contributor.authorIljazovic, Aida
dc.contributor.authorSarter, Kerstin
dc.contributor.authorAlbrecht, Olivia
dc.contributor.authorSchulz, Oscar
dc.contributor.authorKrishnacoumar, Brenda
dc.contributor.authorKrönke, Gerhard
dc.contributor.authorHerrmann, Martin
dc.contributor.authorMougiakakos, Dimitrios
dc.contributor.authorStrowig, Till
dc.contributor.authorSchett, Georg
dc.contributor.authorZaiss, Mario M
dc.date.accessioned2018-01-16T08:49:05Z
dc.date.available2018-01-16T08:49:05Z
dc.date.issued2018
dc.identifier.citationShort-chain fatty acids regulate systemic bone mass and protect from pathological bone loss. 2018, 9 (1):55 Nat Communen
dc.identifier.issn2041-1723
dc.identifier.pmid29302038
dc.identifier.doi10.1038/s41467-017-02490-4
dc.identifier.urihttp://hdl.handle.net/10033/621233
dc.description.abstractMicrobial 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.
dc.language.isoenen
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/*
dc.titleShort-chain fatty acids regulate systemic bone mass and protect from pathological bone loss.en
dc.typeArticleen
dc.contributor.departmentHelmholtz-Zentrum für Infektionsforschung GmbH, Inhoffenstr. 7, 38124 Braunschweig, Germany.en
dc.identifier.journalNature communicationsen
refterms.dateFOA2018-06-13T09:04:17Z
html.description.abstractMicrobial 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.


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