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The essential roles of FXR in diet and age influenced metabolic changes and liver disease development: a multi-omics study
BACKGROUND: Aging and diet are risks for metabolic diseases. Bile acid receptor farnesoid X receptor (FXR) knockout (KO) mice develop metabolic liver diseases that progress into cancer as they age, which is accelerated by Western diet (WD) intake. The current study uncovers the molecular signatures...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9938992/ https://www.ncbi.nlm.nih.gov/pubmed/36803569 http://dx.doi.org/10.1186/s40364-023-00458-9 |
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author | Yang, Guiyan Jena, Prasant K. Hu, Ying Sheng, Lili Chen, Shin-Yu Slupsky, Carolyn M. Davis, Ryan Tepper, Clifford G. Wan, Yu-Jui Yvonne |
author_facet | Yang, Guiyan Jena, Prasant K. Hu, Ying Sheng, Lili Chen, Shin-Yu Slupsky, Carolyn M. Davis, Ryan Tepper, Clifford G. Wan, Yu-Jui Yvonne |
author_sort | Yang, Guiyan |
collection | PubMed |
description | BACKGROUND: Aging and diet are risks for metabolic diseases. Bile acid receptor farnesoid X receptor (FXR) knockout (KO) mice develop metabolic liver diseases that progress into cancer as they age, which is accelerated by Western diet (WD) intake. The current study uncovers the molecular signatures for diet and age-linked metabolic liver disease development in an FXR-dependent manner. METHODS: Wild-type (WT) and FXR KO male mice, either on a healthy control diet (CD) or a WD, were euthanized at the ages of 5, 10, or 15 months. Hepatic transcriptomics, liver, serum, and urine metabolomics as well as microbiota were profiled. RESULTS: WD intake facilitated hepatic aging in WT mice. In an FXR-dependent manner, increased inflammation and reduced oxidative phosphorylation were the primary pathways affected by WD and aging. FXR has a role in modulating inflammation and B cell-mediated humoral immunity which was enhanced by aging. Moreover, FXR dictated neuron differentiation, muscle contraction, and cytoskeleton organization in addition to metabolism. There were 654 transcripts commonly altered by diets, ages, and FXR KO, and 76 of them were differentially expressed in human hepatocellular carcinoma (HCC) and healthy livers. Urine metabolites differentiated dietary effects in both genotypes, and serum metabolites clearly separated ages irrespective of diets. Aging and FXR KO commonly affected amino acid metabolism and TCA cycle. Moreover, FXR is essential for colonization of age-related gut microbes. Integrated analyses uncovered metabolites and bacteria linked with hepatic transcripts affected by WD intake, aging, and FXR KO as well as related to HCC patient survival. CONCLUSION: FXR is a target to prevent diet or age-associated metabolic disease. The uncovered metabolites and microbes can be diagnostic markers for metabolic disease. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40364-023-00458-9. |
format | Online Article Text |
id | pubmed-9938992 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-99389922023-02-20 The essential roles of FXR in diet and age influenced metabolic changes and liver disease development: a multi-omics study Yang, Guiyan Jena, Prasant K. Hu, Ying Sheng, Lili Chen, Shin-Yu Slupsky, Carolyn M. Davis, Ryan Tepper, Clifford G. Wan, Yu-Jui Yvonne Biomark Res Research BACKGROUND: Aging and diet are risks for metabolic diseases. Bile acid receptor farnesoid X receptor (FXR) knockout (KO) mice develop metabolic liver diseases that progress into cancer as they age, which is accelerated by Western diet (WD) intake. The current study uncovers the molecular signatures for diet and age-linked metabolic liver disease development in an FXR-dependent manner. METHODS: Wild-type (WT) and FXR KO male mice, either on a healthy control diet (CD) or a WD, were euthanized at the ages of 5, 10, or 15 months. Hepatic transcriptomics, liver, serum, and urine metabolomics as well as microbiota were profiled. RESULTS: WD intake facilitated hepatic aging in WT mice. In an FXR-dependent manner, increased inflammation and reduced oxidative phosphorylation were the primary pathways affected by WD and aging. FXR has a role in modulating inflammation and B cell-mediated humoral immunity which was enhanced by aging. Moreover, FXR dictated neuron differentiation, muscle contraction, and cytoskeleton organization in addition to metabolism. There were 654 transcripts commonly altered by diets, ages, and FXR KO, and 76 of them were differentially expressed in human hepatocellular carcinoma (HCC) and healthy livers. Urine metabolites differentiated dietary effects in both genotypes, and serum metabolites clearly separated ages irrespective of diets. Aging and FXR KO commonly affected amino acid metabolism and TCA cycle. Moreover, FXR is essential for colonization of age-related gut microbes. Integrated analyses uncovered metabolites and bacteria linked with hepatic transcripts affected by WD intake, aging, and FXR KO as well as related to HCC patient survival. CONCLUSION: FXR is a target to prevent diet or age-associated metabolic disease. The uncovered metabolites and microbes can be diagnostic markers for metabolic disease. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40364-023-00458-9. BioMed Central 2023-02-18 /pmc/articles/PMC9938992/ /pubmed/36803569 http://dx.doi.org/10.1186/s40364-023-00458-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Yang, Guiyan Jena, Prasant K. Hu, Ying Sheng, Lili Chen, Shin-Yu Slupsky, Carolyn M. Davis, Ryan Tepper, Clifford G. Wan, Yu-Jui Yvonne The essential roles of FXR in diet and age influenced metabolic changes and liver disease development: a multi-omics study |
title | The essential roles of FXR in diet and age influenced metabolic changes and liver disease development: a multi-omics study |
title_full | The essential roles of FXR in diet and age influenced metabolic changes and liver disease development: a multi-omics study |
title_fullStr | The essential roles of FXR in diet and age influenced metabolic changes and liver disease development: a multi-omics study |
title_full_unstemmed | The essential roles of FXR in diet and age influenced metabolic changes and liver disease development: a multi-omics study |
title_short | The essential roles of FXR in diet and age influenced metabolic changes and liver disease development: a multi-omics study |
title_sort | essential roles of fxr in diet and age influenced metabolic changes and liver disease development: a multi-omics study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9938992/ https://www.ncbi.nlm.nih.gov/pubmed/36803569 http://dx.doi.org/10.1186/s40364-023-00458-9 |
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