Cargando…

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 (...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
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
_version_ 1784636536251219968
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
work_keys_str_mv AT kirklmadison exploitingthreedimensionalhumanhepaticconstructstoinvestigatetheimpactofrs174537onfattyacidmetabolism
AT waitscharlottemaek exploitingthreedimensionalhumanhepaticconstructstoinvestigatetheimpactofrs174537onfattyacidmetabolism
AT bashorealexanderc exploitingthreedimensionalhumanhepaticconstructstoinvestigatetheimpactofrs174537onfattyacidmetabolism
AT dossobeverly exploitingthreedimensionalhumanhepaticconstructstoinvestigatetheimpactofrs174537onfattyacidmetabolism
AT meyersallisonk exploitingthreedimensionalhumanhepaticconstructstoinvestigatetheimpactofrs174537onfattyacidmetabolism
AT renaldoantonioc exploitingthreedimensionalhumanhepaticconstructstoinvestigatetheimpactofrs174537onfattyacidmetabolism
AT depalmathomasj exploitingthreedimensionalhumanhepaticconstructstoinvestigatetheimpactofrs174537onfattyacidmetabolism
AT simmskellin exploitingthreedimensionalhumanhepaticconstructstoinvestigatetheimpactofrs174537onfattyacidmetabolism
AT hausernathaniel exploitingthreedimensionalhumanhepaticconstructstoinvestigatetheimpactofrs174537onfattyacidmetabolism
AT chuangkeychiachi exploitingthreedimensionalhumanhepaticconstructstoinvestigatetheimpactofrs174537onfattyacidmetabolism
AT mccallcharlese exploitingthreedimensionalhumanhepaticconstructstoinvestigatetheimpactofrs174537onfattyacidmetabolism
AT parksjohns exploitingthreedimensionalhumanhepaticconstructstoinvestigatetheimpactofrs174537onfattyacidmetabolism
AT sergeantsusan exploitingthreedimensionalhumanhepaticconstructstoinvestigatetheimpactofrs174537onfattyacidmetabolism
AT langefeldcarld exploitingthreedimensionalhumanhepaticconstructstoinvestigatetheimpactofrs174537onfattyacidmetabolism
AT skardalaleksander exploitingthreedimensionalhumanhepaticconstructstoinvestigatetheimpactofrs174537onfattyacidmetabolism
AT rahbarelaheh exploitingthreedimensionalhumanhepaticconstructstoinvestigatetheimpactofrs174537onfattyacidmetabolism