The pregnane X receptor drives sexually dimorphic hepatic changes in lipid and xenobiotic metabolism in response to gut microbiota in mice

Abstract Background The gut microbiota–intestine–liver relationship is emerging as an important factor in multiple hepatic pathologies, but the hepatic sensors and effectors of microbial signals are not well defined. Results By comparing publicly available liver transcriptomics data from conventiona...

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Main Authors: Sharon Ann Barretto, Frederic Lasserre, Marine Huillet, Marion Régnier, Arnaud Polizzi, Yannick Lippi, Anne Fougerat, Elodie Person, Sandrine Bruel, Colette Bétoulières, Claire Naylies, Céline Lukowicz, Sarra Smati, Laurence Guzylack, Maïwenn Olier, Vassilia Théodorou, Laila Mselli-Lakhal, Daniel Zalko, Walter Wahli, Nicolas Loiseau, Laurence Gamet-Payrastre, Hervé Guillou, Sandrine Ellero-Simatos
Format: Article
Language:English
Published: BMC 2021-04-01
Series:Microbiome
Subjects:
Online Access:https://doi.org/10.1186/s40168-021-01050-9
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language English
format Article
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author Sharon Ann Barretto
Frederic Lasserre
Marine Huillet
Marion Régnier
Arnaud Polizzi
Yannick Lippi
Anne Fougerat
Elodie Person
Sandrine Bruel
Colette Bétoulières
Claire Naylies
Céline Lukowicz
Sarra Smati
Laurence Guzylack
Maïwenn Olier
Vassilia Théodorou
Laila Mselli-Lakhal
Daniel Zalko
Walter Wahli
Nicolas Loiseau
Laurence Gamet-Payrastre
Hervé Guillou
Sandrine Ellero-Simatos
spellingShingle Sharon Ann Barretto
Frederic Lasserre
Marine Huillet
Marion Régnier
Arnaud Polizzi
Yannick Lippi
Anne Fougerat
Elodie Person
Sandrine Bruel
Colette Bétoulières
Claire Naylies
Céline Lukowicz
Sarra Smati
Laurence Guzylack
Maïwenn Olier
Vassilia Théodorou
Laila Mselli-Lakhal
Daniel Zalko
Walter Wahli
Nicolas Loiseau
Laurence Gamet-Payrastre
Hervé Guillou
Sandrine Ellero-Simatos
The pregnane X receptor drives sexually dimorphic hepatic changes in lipid and xenobiotic metabolism in response to gut microbiota in mice
Microbiome
Gut microbiota
Liver
Pregnane X receptor
NR1I2
Xenobiotic metabolism
Fatty acid metabolism
author_facet Sharon Ann Barretto
Frederic Lasserre
Marine Huillet
Marion Régnier
Arnaud Polizzi
Yannick Lippi
Anne Fougerat
Elodie Person
Sandrine Bruel
Colette Bétoulières
Claire Naylies
Céline Lukowicz
Sarra Smati
Laurence Guzylack
Maïwenn Olier
Vassilia Théodorou
Laila Mselli-Lakhal
Daniel Zalko
Walter Wahli
Nicolas Loiseau
Laurence Gamet-Payrastre
Hervé Guillou
Sandrine Ellero-Simatos
author_sort Sharon Ann Barretto
title The pregnane X receptor drives sexually dimorphic hepatic changes in lipid and xenobiotic metabolism in response to gut microbiota in mice
title_short The pregnane X receptor drives sexually dimorphic hepatic changes in lipid and xenobiotic metabolism in response to gut microbiota in mice
title_full The pregnane X receptor drives sexually dimorphic hepatic changes in lipid and xenobiotic metabolism in response to gut microbiota in mice
title_fullStr The pregnane X receptor drives sexually dimorphic hepatic changes in lipid and xenobiotic metabolism in response to gut microbiota in mice
title_full_unstemmed The pregnane X receptor drives sexually dimorphic hepatic changes in lipid and xenobiotic metabolism in response to gut microbiota in mice
title_sort pregnane x receptor drives sexually dimorphic hepatic changes in lipid and xenobiotic metabolism in response to gut microbiota in mice
publisher BMC
series Microbiome
issn 2049-2618
publishDate 2021-04-01
description Abstract Background The gut microbiota–intestine–liver relationship is emerging as an important factor in multiple hepatic pathologies, but the hepatic sensors and effectors of microbial signals are not well defined. Results By comparing publicly available liver transcriptomics data from conventional vs. germ-free mice, we identified pregnane X receptor (PXR, NR1I2) transcriptional activity as strongly affected by the absence of gut microbes. Microbiota depletion using antibiotics in Pxr +/+ vs Pxr -/- C57BL/6J littermate mice followed by hepatic transcriptomics revealed that most microbiota-sensitive genes were PXR-dependent in the liver in males, but not in females. Pathway enrichment analysis suggested that microbiota–PXR interaction controlled fatty acid and xenobiotic metabolism. We confirmed that antibiotic treatment reduced liver triglyceride content and hampered xenobiotic metabolism in the liver from Pxr +/+ but not Pxr -/- male mice. Conclusions These findings identify PXR as a hepatic effector of microbiota-derived signals that regulate the host’s sexually dimorphic lipid and xenobiotic metabolisms in the liver. Thus, our results reveal a potential new mechanism for unexpected drug–drug or food–drug interactions. Video abstract
topic Gut microbiota
Liver
Pregnane X receptor
NR1I2
Xenobiotic metabolism
Fatty acid metabolism
url https://doi.org/10.1186/s40168-021-01050-9
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spelling doaj-12bed86311cd49f3af2cf456cbbcc32d2021-04-25T11:46:17ZengBMCMicrobiome2049-26182021-04-019111610.1186/s40168-021-01050-9The pregnane X receptor drives sexually dimorphic hepatic changes in lipid and xenobiotic metabolism in response to gut microbiota in miceSharon Ann Barretto0Frederic Lasserre1Marine Huillet2Marion Régnier3Arnaud Polizzi4Yannick Lippi5Anne Fougerat6Elodie Person7Sandrine Bruel8Colette Bétoulières9Claire Naylies10Céline Lukowicz11Sarra Smati12Laurence Guzylack13Maïwenn Olier14Vassilia Théodorou15Laila Mselli-Lakhal16Daniel Zalko17Walter Wahli18Nicolas Loiseau19Laurence Gamet-Payrastre20Hervé Guillou21Sandrine Ellero-Simatos22Toxalim (Research Centre in Food Toxicology), INRAE, ENVT, INP-Purpan, UPS, Université de ToulouseToxalim (Research Centre in Food Toxicology), INRAE, ENVT, INP-Purpan, UPS, Université de ToulouseToxalim (Research Centre in Food Toxicology), INRAE, ENVT, INP-Purpan, UPS, Université de ToulouseToxalim (Research Centre in Food Toxicology), INRAE, ENVT, INP-Purpan, UPS, Université de ToulouseToxalim (Research Centre in Food Toxicology), INRAE, ENVT, INP-Purpan, UPS, Université de ToulouseToxalim (Research Centre in Food Toxicology), INRAE, ENVT, INP-Purpan, UPS, Université de ToulouseToxalim (Research Centre in Food Toxicology), INRAE, ENVT, INP-Purpan, UPS, Université de ToulouseToxalim (Research Centre in Food Toxicology), INRAE, ENVT, INP-Purpan, UPS, Université de ToulouseToxalim (Research Centre in Food Toxicology), INRAE, ENVT, INP-Purpan, UPS, Université de ToulouseToxalim (Research Centre in Food Toxicology), INRAE, ENVT, INP-Purpan, UPS, Université de ToulouseToxalim (Research Centre in Food Toxicology), INRAE, ENVT, INP-Purpan, UPS, Université de ToulouseToxalim (Research Centre in Food Toxicology), INRAE, ENVT, INP-Purpan, UPS, Université de ToulouseToxalim (Research Centre in Food Toxicology), INRAE, ENVT, INP-Purpan, UPS, Université de ToulouseToxalim (Research Centre in Food Toxicology), INRAE, ENVT, INP-Purpan, UPS, Université de ToulouseToxalim (Research Centre in Food Toxicology), INRAE, ENVT, INP-Purpan, UPS, Université de ToulouseToxalim (Research Centre in Food Toxicology), INRAE, ENVT, INP-Purpan, UPS, Université de ToulouseToxalim (Research Centre in Food Toxicology), INRAE, ENVT, INP-Purpan, UPS, Université de ToulouseToxalim (Research Centre in Food Toxicology), INRAE, ENVT, INP-Purpan, UPS, Université de ToulouseToxalim (Research Centre in Food Toxicology), INRAE, ENVT, INP-Purpan, UPS, Université de ToulouseToxalim (Research Centre in Food Toxicology), INRAE, ENVT, INP-Purpan, UPS, Université de ToulouseToxalim (Research Centre in Food Toxicology), INRAE, ENVT, INP-Purpan, UPS, Université de ToulouseToxalim (Research Centre in Food Toxicology), INRAE, ENVT, INP-Purpan, UPS, Université de ToulouseToxalim (Research Centre in Food Toxicology), INRAE, ENVT, INP-Purpan, UPS, Université de ToulouseAbstract Background The gut microbiota–intestine–liver relationship is emerging as an important factor in multiple hepatic pathologies, but the hepatic sensors and effectors of microbial signals are not well defined. Results By comparing publicly available liver transcriptomics data from conventional vs. germ-free mice, we identified pregnane X receptor (PXR, NR1I2) transcriptional activity as strongly affected by the absence of gut microbes. Microbiota depletion using antibiotics in Pxr +/+ vs Pxr -/- C57BL/6J littermate mice followed by hepatic transcriptomics revealed that most microbiota-sensitive genes were PXR-dependent in the liver in males, but not in females. Pathway enrichment analysis suggested that microbiota–PXR interaction controlled fatty acid and xenobiotic metabolism. We confirmed that antibiotic treatment reduced liver triglyceride content and hampered xenobiotic metabolism in the liver from Pxr +/+ but not Pxr -/- male mice. Conclusions These findings identify PXR as a hepatic effector of microbiota-derived signals that regulate the host’s sexually dimorphic lipid and xenobiotic metabolisms in the liver. Thus, our results reveal a potential new mechanism for unexpected drug–drug or food–drug interactions. Video abstracthttps://doi.org/10.1186/s40168-021-01050-9Gut microbiotaLiverPregnane X receptorNR1I2Xenobiotic metabolismFatty acid metabolism