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Akkermansia muciniphila mediates negative effects of IFNγ on glucose metabolism

Cross-talk between the gut microbiota and the host immune system regulates host metabolism, and its dysregulation can cause metabolic disease. Here, we show that the gut microbe Akkermansia muciniphila can mediate negative effects of IFNγ on glucose tolerance. In IFNγ-deficient mice, A. muciniphila...

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Autores principales: Greer, Renee L., Dong, Xiaoxi, Moraes, Ana Carolina F., Zielke, Ryszard A., Fernandes, Gabriel R., Peremyslova, Ekaterina, Vasquez-Perez, Stephany, Schoenborn, Alexi A., Gomes, Everton P., Pereira, Alexandre C., Ferreira, Sandra R. G., Yao, Michael, Fuss, Ivan J., Strober, Warren, Sikora, Aleksandra E., Taylor, Gregory A., Gulati, Ajay S., Morgun, Andrey, Shulzhenko, Natalia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5114536/
https://www.ncbi.nlm.nih.gov/pubmed/27841267
http://dx.doi.org/10.1038/ncomms13329
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author Greer, Renee L.
Dong, Xiaoxi
Moraes, Ana Carolina F.
Zielke, Ryszard A.
Fernandes, Gabriel R.
Peremyslova, Ekaterina
Vasquez-Perez, Stephany
Schoenborn, Alexi A.
Gomes, Everton P.
Pereira, Alexandre C.
Ferreira, Sandra R. G.
Yao, Michael
Fuss, Ivan J.
Strober, Warren
Sikora, Aleksandra E.
Taylor, Gregory A.
Gulati, Ajay S.
Morgun, Andrey
Shulzhenko, Natalia
author_facet Greer, Renee L.
Dong, Xiaoxi
Moraes, Ana Carolina F.
Zielke, Ryszard A.
Fernandes, Gabriel R.
Peremyslova, Ekaterina
Vasquez-Perez, Stephany
Schoenborn, Alexi A.
Gomes, Everton P.
Pereira, Alexandre C.
Ferreira, Sandra R. G.
Yao, Michael
Fuss, Ivan J.
Strober, Warren
Sikora, Aleksandra E.
Taylor, Gregory A.
Gulati, Ajay S.
Morgun, Andrey
Shulzhenko, Natalia
author_sort Greer, Renee L.
collection PubMed
description Cross-talk between the gut microbiota and the host immune system regulates host metabolism, and its dysregulation can cause metabolic disease. Here, we show that the gut microbe Akkermansia muciniphila can mediate negative effects of IFNγ on glucose tolerance. In IFNγ-deficient mice, A. muciniphila is significantly increased and restoration of IFNγ levels reduces A. muciniphila abundance. We further show that IFNγ-knockout mice whose microbiota does not contain A. muciniphila do not show improvement in glucose tolerance and adding back A. muciniphila promoted enhanced glucose tolerance. We go on to identify Irgm1 as an IFNγ-regulated gene in the mouse ileum that controls gut A. muciniphila levels. A. muciniphila is also linked to IFNγ-regulated gene expression in the intestine and glucose parameters in humans, suggesting that this trialogue between IFNγ, A. muciniphila and glucose tolerance might be an evolutionally conserved mechanism regulating metabolic health in mice and humans.
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spelling pubmed-51145362016-11-29 Akkermansia muciniphila mediates negative effects of IFNγ on glucose metabolism Greer, Renee L. Dong, Xiaoxi Moraes, Ana Carolina F. Zielke, Ryszard A. Fernandes, Gabriel R. Peremyslova, Ekaterina Vasquez-Perez, Stephany Schoenborn, Alexi A. Gomes, Everton P. Pereira, Alexandre C. Ferreira, Sandra R. G. Yao, Michael Fuss, Ivan J. Strober, Warren Sikora, Aleksandra E. Taylor, Gregory A. Gulati, Ajay S. Morgun, Andrey Shulzhenko, Natalia Nat Commun Article Cross-talk between the gut microbiota and the host immune system regulates host metabolism, and its dysregulation can cause metabolic disease. Here, we show that the gut microbe Akkermansia muciniphila can mediate negative effects of IFNγ on glucose tolerance. In IFNγ-deficient mice, A. muciniphila is significantly increased and restoration of IFNγ levels reduces A. muciniphila abundance. We further show that IFNγ-knockout mice whose microbiota does not contain A. muciniphila do not show improvement in glucose tolerance and adding back A. muciniphila promoted enhanced glucose tolerance. We go on to identify Irgm1 as an IFNγ-regulated gene in the mouse ileum that controls gut A. muciniphila levels. A. muciniphila is also linked to IFNγ-regulated gene expression in the intestine and glucose parameters in humans, suggesting that this trialogue between IFNγ, A. muciniphila and glucose tolerance might be an evolutionally conserved mechanism regulating metabolic health in mice and humans. Nature Publishing Group 2016-11-14 /pmc/articles/PMC5114536/ /pubmed/27841267 http://dx.doi.org/10.1038/ncomms13329 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Greer, Renee L.
Dong, Xiaoxi
Moraes, Ana Carolina F.
Zielke, Ryszard A.
Fernandes, Gabriel R.
Peremyslova, Ekaterina
Vasquez-Perez, Stephany
Schoenborn, Alexi A.
Gomes, Everton P.
Pereira, Alexandre C.
Ferreira, Sandra R. G.
Yao, Michael
Fuss, Ivan J.
Strober, Warren
Sikora, Aleksandra E.
Taylor, Gregory A.
Gulati, Ajay S.
Morgun, Andrey
Shulzhenko, Natalia
Akkermansia muciniphila mediates negative effects of IFNγ on glucose metabolism
title Akkermansia muciniphila mediates negative effects of IFNγ on glucose metabolism
title_full Akkermansia muciniphila mediates negative effects of IFNγ on glucose metabolism
title_fullStr Akkermansia muciniphila mediates negative effects of IFNγ on glucose metabolism
title_full_unstemmed Akkermansia muciniphila mediates negative effects of IFNγ on glucose metabolism
title_short Akkermansia muciniphila mediates negative effects of IFNγ on glucose metabolism
title_sort akkermansia muciniphila mediates negative effects of ifnγ on glucose metabolism
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5114536/
https://www.ncbi.nlm.nih.gov/pubmed/27841267
http://dx.doi.org/10.1038/ncomms13329
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