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Exploiting three-dimensional human hepatic constructs to investigate the impact of rs174537 on fatty acid metabolism
The Modern Western Diet has been associated with the rise in metabolic and inflammatory diseases, including obesity, diabetes, and cardiovascular disease. This has been attributed, in part, to the increase in dietary omega-6 polyunsaturated fatty acid (PUFA) consumption, specifically linoleic acid (...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8775235/ https://www.ncbi.nlm.nih.gov/pubmed/35051193 http://dx.doi.org/10.1371/journal.pone.0262173 |
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author | Kirk, L. Madison Waits, Charlotte Mae K. Bashore, Alexander C. Dosso, Beverly Meyers, Allison K. Renaldo, Antonio C. DePalma, Thomas J. Simms, Kelli N. Hauser, Nathaniel Chuang Key, Chia-Chi McCall, Charles E. Parks, John S. Sergeant, Susan Langefeld, Carl D. Skardal, Aleksander Rahbar, Elaheh |
author_facet | Kirk, L. Madison Waits, Charlotte Mae K. Bashore, Alexander C. Dosso, Beverly Meyers, Allison K. Renaldo, Antonio C. DePalma, Thomas J. Simms, Kelli N. Hauser, Nathaniel Chuang Key, Chia-Chi McCall, Charles E. Parks, John S. Sergeant, Susan Langefeld, Carl D. Skardal, Aleksander Rahbar, Elaheh |
author_sort | Kirk, L. Madison |
collection | PubMed |
description | The Modern Western Diet has been associated with the rise in metabolic and inflammatory diseases, including obesity, diabetes, and cardiovascular disease. This has been attributed, in part, to the increase in dietary omega-6 polyunsaturated fatty acid (PUFA) consumption, specifically linoleic acid (LA), arachidonic acid (ARA), and their subsequent metabolism to pro-inflammatory metabolites which may be driving human disease. Conversion of dietary LA to ARA is regulated by genetic variants near and within the fatty acid desaturase (FADS) haplotype block, most notably single nucleotide polymorphism rs174537 is strongly associated with FADS1 activity and expression. This variant and others within high linkage disequilibrium may potentially explain the diversity in both diet and inflammatory mediators that drive chronic inflammatory disease in human populations. Mechanistic exploration into this phenomenon using human hepatocytes is limited by current two-dimensional culture models that poorly replicate in vivo functionality. Therefore, we aimed to develop and characterize a three-dimensional hepatic construct for the study of human PUFA metabolism. Primary human hepatocytes cultured in 3D hydrogels were characterized for their capacity to represent basic lipid processing functions, including lipid esterification, de novo lipogenesis, and cholesterol efflux. They were then exposed to control and LA-enriched media and reproducibly displayed allele-specific metabolic activity of FADS1, based on genotype at rs174537. Hepatocytes derived from individuals homozygous with the minor allele at rs174537 (i.e., TT) displayed the slowest metabolic conversion of LA to ARA and significantly reduced FADS1 and FADS2 expression. These results support the feasibility of using 3D human hepatic cultures for the study of human PUFA and lipid metabolism and relevant gene-diet interactions, thereby enabling future nutrition targets in humans. |
format | Online Article Text |
id | pubmed-8775235 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-87752352022-01-21 Exploiting three-dimensional human hepatic constructs to investigate the impact of rs174537 on fatty acid metabolism Kirk, L. Madison Waits, Charlotte Mae K. Bashore, Alexander C. Dosso, Beverly Meyers, Allison K. Renaldo, Antonio C. DePalma, Thomas J. Simms, Kelli N. Hauser, Nathaniel Chuang Key, Chia-Chi McCall, Charles E. Parks, John S. Sergeant, Susan Langefeld, Carl D. Skardal, Aleksander Rahbar, Elaheh PLoS One Research Article The Modern Western Diet has been associated with the rise in metabolic and inflammatory diseases, including obesity, diabetes, and cardiovascular disease. This has been attributed, in part, to the increase in dietary omega-6 polyunsaturated fatty acid (PUFA) consumption, specifically linoleic acid (LA), arachidonic acid (ARA), and their subsequent metabolism to pro-inflammatory metabolites which may be driving human disease. Conversion of dietary LA to ARA is regulated by genetic variants near and within the fatty acid desaturase (FADS) haplotype block, most notably single nucleotide polymorphism rs174537 is strongly associated with FADS1 activity and expression. This variant and others within high linkage disequilibrium may potentially explain the diversity in both diet and inflammatory mediators that drive chronic inflammatory disease in human populations. Mechanistic exploration into this phenomenon using human hepatocytes is limited by current two-dimensional culture models that poorly replicate in vivo functionality. Therefore, we aimed to develop and characterize a three-dimensional hepatic construct for the study of human PUFA metabolism. Primary human hepatocytes cultured in 3D hydrogels were characterized for their capacity to represent basic lipid processing functions, including lipid esterification, de novo lipogenesis, and cholesterol efflux. They were then exposed to control and LA-enriched media and reproducibly displayed allele-specific metabolic activity of FADS1, based on genotype at rs174537. Hepatocytes derived from individuals homozygous with the minor allele at rs174537 (i.e., TT) displayed the slowest metabolic conversion of LA to ARA and significantly reduced FADS1 and FADS2 expression. These results support the feasibility of using 3D human hepatic cultures for the study of human PUFA and lipid metabolism and relevant gene-diet interactions, thereby enabling future nutrition targets in humans. Public Library of Science 2022-01-20 /pmc/articles/PMC8775235/ /pubmed/35051193 http://dx.doi.org/10.1371/journal.pone.0262173 Text en © 2022 Kirk et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Kirk, L. Madison Waits, Charlotte Mae K. Bashore, Alexander C. Dosso, Beverly Meyers, Allison K. Renaldo, Antonio C. DePalma, Thomas J. Simms, Kelli N. Hauser, Nathaniel Chuang Key, Chia-Chi McCall, Charles E. Parks, John S. Sergeant, Susan Langefeld, Carl D. Skardal, Aleksander Rahbar, Elaheh Exploiting three-dimensional human hepatic constructs to investigate the impact of rs174537 on fatty acid metabolism |
title | Exploiting three-dimensional human hepatic constructs to investigate the impact of rs174537 on fatty acid metabolism |
title_full | Exploiting three-dimensional human hepatic constructs to investigate the impact of rs174537 on fatty acid metabolism |
title_fullStr | Exploiting three-dimensional human hepatic constructs to investigate the impact of rs174537 on fatty acid metabolism |
title_full_unstemmed | Exploiting three-dimensional human hepatic constructs to investigate the impact of rs174537 on fatty acid metabolism |
title_short | Exploiting three-dimensional human hepatic constructs to investigate the impact of rs174537 on fatty acid metabolism |
title_sort | exploiting three-dimensional human hepatic constructs to investigate the impact of rs174537 on fatty acid metabolism |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8775235/ https://www.ncbi.nlm.nih.gov/pubmed/35051193 http://dx.doi.org/10.1371/journal.pone.0262173 |
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