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A stem cell based in vitro model of NAFLD enables the analysis of patient specific individual metabolic adaptations in response to a high fat diet and AdipoRon interference
Non-alcoholic fatty liver disease (NAFLD) is a multifactorial disease. Its development and progression depend on genetically predisposed susceptibility of the patient towards several ‘hits’ that induce fat storage first and later inflammation and fibrosis. Here, we differentiated induced pluripotent...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7860118/ https://www.ncbi.nlm.nih.gov/pubmed/33372064 http://dx.doi.org/10.1242/bio.054189 |
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author | Graffmann, Nina Ncube, Audrey Martins, Soraia Fiszl, Aurelian Robert Reuther, Philipp Bohndorf, Martina Wruck, Wasco Beller, Mathias Czekelius, Constantin Adjaye, James |
author_facet | Graffmann, Nina Ncube, Audrey Martins, Soraia Fiszl, Aurelian Robert Reuther, Philipp Bohndorf, Martina Wruck, Wasco Beller, Mathias Czekelius, Constantin Adjaye, James |
author_sort | Graffmann, Nina |
collection | PubMed |
description | Non-alcoholic fatty liver disease (NAFLD) is a multifactorial disease. Its development and progression depend on genetically predisposed susceptibility of the patient towards several ‘hits’ that induce fat storage first and later inflammation and fibrosis. Here, we differentiated induced pluripotent stem cells (iPSCs) derived from four distinct donors with varying disease stages into hepatocyte like cells (HLCs) and determined fat storage as well as metabolic adaptations after stimulations with oleic acid. We could recapitulate the complex networks that control lipid and glucose metabolism and we identified distinct gene expression profiles related to the steatosis phenotype of the donor. In an attempt to reverse the steatotic phenotype, cells were treated with the small molecule AdipoRon, a synthetic analogue of adiponectin. Although the responses varied between cells lines, they suggest a general influence of AdipoRon on metabolism, transport, immune system, cell stress and signalling. |
format | Online Article Text |
id | pubmed-7860118 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-78601182021-02-04 A stem cell based in vitro model of NAFLD enables the analysis of patient specific individual metabolic adaptations in response to a high fat diet and AdipoRon interference Graffmann, Nina Ncube, Audrey Martins, Soraia Fiszl, Aurelian Robert Reuther, Philipp Bohndorf, Martina Wruck, Wasco Beller, Mathias Czekelius, Constantin Adjaye, James Biol Open Research Article Non-alcoholic fatty liver disease (NAFLD) is a multifactorial disease. Its development and progression depend on genetically predisposed susceptibility of the patient towards several ‘hits’ that induce fat storage first and later inflammation and fibrosis. Here, we differentiated induced pluripotent stem cells (iPSCs) derived from four distinct donors with varying disease stages into hepatocyte like cells (HLCs) and determined fat storage as well as metabolic adaptations after stimulations with oleic acid. We could recapitulate the complex networks that control lipid and glucose metabolism and we identified distinct gene expression profiles related to the steatosis phenotype of the donor. In an attempt to reverse the steatotic phenotype, cells were treated with the small molecule AdipoRon, a synthetic analogue of adiponectin. Although the responses varied between cells lines, they suggest a general influence of AdipoRon on metabolism, transport, immune system, cell stress and signalling. The Company of Biologists Ltd 2021-01-25 /pmc/articles/PMC7860118/ /pubmed/33372064 http://dx.doi.org/10.1242/bio.054189 Text en © 2021. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/4.0This 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 that the original work is properly attributed. |
spellingShingle | Research Article Graffmann, Nina Ncube, Audrey Martins, Soraia Fiszl, Aurelian Robert Reuther, Philipp Bohndorf, Martina Wruck, Wasco Beller, Mathias Czekelius, Constantin Adjaye, James A stem cell based in vitro model of NAFLD enables the analysis of patient specific individual metabolic adaptations in response to a high fat diet and AdipoRon interference |
title | A stem cell based in vitro model of NAFLD enables the analysis of patient specific individual metabolic adaptations in response to a high fat diet and AdipoRon interference |
title_full | A stem cell based in vitro model of NAFLD enables the analysis of patient specific individual metabolic adaptations in response to a high fat diet and AdipoRon interference |
title_fullStr | A stem cell based in vitro model of NAFLD enables the analysis of patient specific individual metabolic adaptations in response to a high fat diet and AdipoRon interference |
title_full_unstemmed | A stem cell based in vitro model of NAFLD enables the analysis of patient specific individual metabolic adaptations in response to a high fat diet and AdipoRon interference |
title_short | A stem cell based in vitro model of NAFLD enables the analysis of patient specific individual metabolic adaptations in response to a high fat diet and AdipoRon interference |
title_sort | stem cell based in vitro model of nafld enables the analysis of patient specific individual metabolic adaptations in response to a high fat diet and adiporon interference |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7860118/ https://www.ncbi.nlm.nih.gov/pubmed/33372064 http://dx.doi.org/10.1242/bio.054189 |
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