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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2021-04-01
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Online Access: | https://doi.org/10.1186/s40168-021-01050-9 |
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DOAJ |
language |
English |
format |
Article |
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DOAJ |
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 |
work_keys_str_mv |
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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 |