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Integrated-gut-liver-on-a-chip platform as an in vitro human model of non-alcoholic fatty liver disease
Non-alcoholic fatty liver disease (NAFLD) afflicts a significant percentage of the population; however, no effective treatments have yet been established because of the unsuitability of in vitro assays and animal experimental models. Here, we present an integrated-gut-liver-on-a-chip (iGLC) platform...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10036655/ https://www.ncbi.nlm.nih.gov/pubmed/36959276 http://dx.doi.org/10.1038/s42003-023-04710-8 |
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author | Yang, Jiandong Hirai, Yoshikazu Iida, Kei Ito, Shinji Trumm, Marika Terada, Shiho Sakai, Risako Tsuchiya, Toshiyuki Tabata, Osamu Kamei, Ken-ichiro |
author_facet | Yang, Jiandong Hirai, Yoshikazu Iida, Kei Ito, Shinji Trumm, Marika Terada, Shiho Sakai, Risako Tsuchiya, Toshiyuki Tabata, Osamu Kamei, Ken-ichiro |
author_sort | Yang, Jiandong |
collection | PubMed |
description | Non-alcoholic fatty liver disease (NAFLD) afflicts a significant percentage of the population; however, no effective treatments have yet been established because of the unsuitability of in vitro assays and animal experimental models. Here, we present an integrated-gut-liver-on-a-chip (iGLC) platform as an in vitro human model of the gut-liver axis (GLA) by co-culturing human gut and liver cell lines interconnected via microfluidics in a closed circulation loop, for the initiation and progression of NAFLD by treatment with free fatty acids (FFAs) for 1 and 7 days, respectively. Co-cultured Caco-2 gut-mimicking cells and HepG2 hepatocyte-like cells demonstrate the protective effects from apoptosis against FFAs treatment, whereas mono-cultured cells exhibit induced apoptosis. Phenotype and gene expression analyses reveal that the FFAs-treated gut and liver cells accumulated intracellular lipid droplets and show an increase in gene expression associated with a cellular response to copper ions and endoplasmic reticulum stress. As an in vitro human GLA model, the iGLC platform may serve as an alternative to animal experiments for investigating the mechanisms of NAFLD. |
format | Online Article Text |
id | pubmed-10036655 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-100366552023-03-25 Integrated-gut-liver-on-a-chip platform as an in vitro human model of non-alcoholic fatty liver disease Yang, Jiandong Hirai, Yoshikazu Iida, Kei Ito, Shinji Trumm, Marika Terada, Shiho Sakai, Risako Tsuchiya, Toshiyuki Tabata, Osamu Kamei, Ken-ichiro Commun Biol Article Non-alcoholic fatty liver disease (NAFLD) afflicts a significant percentage of the population; however, no effective treatments have yet been established because of the unsuitability of in vitro assays and animal experimental models. Here, we present an integrated-gut-liver-on-a-chip (iGLC) platform as an in vitro human model of the gut-liver axis (GLA) by co-culturing human gut and liver cell lines interconnected via microfluidics in a closed circulation loop, for the initiation and progression of NAFLD by treatment with free fatty acids (FFAs) for 1 and 7 days, respectively. Co-cultured Caco-2 gut-mimicking cells and HepG2 hepatocyte-like cells demonstrate the protective effects from apoptosis against FFAs treatment, whereas mono-cultured cells exhibit induced apoptosis. Phenotype and gene expression analyses reveal that the FFAs-treated gut and liver cells accumulated intracellular lipid droplets and show an increase in gene expression associated with a cellular response to copper ions and endoplasmic reticulum stress. As an in vitro human GLA model, the iGLC platform may serve as an alternative to animal experiments for investigating the mechanisms of NAFLD. Nature Publishing Group UK 2023-03-23 /pmc/articles/PMC10036655/ /pubmed/36959276 http://dx.doi.org/10.1038/s42003-023-04710-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Yang, Jiandong Hirai, Yoshikazu Iida, Kei Ito, Shinji Trumm, Marika Terada, Shiho Sakai, Risako Tsuchiya, Toshiyuki Tabata, Osamu Kamei, Ken-ichiro Integrated-gut-liver-on-a-chip platform as an in vitro human model of non-alcoholic fatty liver disease |
title | Integrated-gut-liver-on-a-chip platform as an in vitro human model of non-alcoholic fatty liver disease |
title_full | Integrated-gut-liver-on-a-chip platform as an in vitro human model of non-alcoholic fatty liver disease |
title_fullStr | Integrated-gut-liver-on-a-chip platform as an in vitro human model of non-alcoholic fatty liver disease |
title_full_unstemmed | Integrated-gut-liver-on-a-chip platform as an in vitro human model of non-alcoholic fatty liver disease |
title_short | Integrated-gut-liver-on-a-chip platform as an in vitro human model of non-alcoholic fatty liver disease |
title_sort | integrated-gut-liver-on-a-chip platform as an in vitro human model of non-alcoholic fatty liver disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10036655/ https://www.ncbi.nlm.nih.gov/pubmed/36959276 http://dx.doi.org/10.1038/s42003-023-04710-8 |
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