Integrated-gut-liver-on-a-chip platform as an in vitro human model of non-alcoholic fatty liver disease

• Published in: Communications biology Vol. 6; no. 1; p. 310
• Main Authors: Yang, Jiandong, Hirai, Yoshikazu, Iida, Kei, Ito, Shinji, Trumm, Marika, Terada, Shiho, Sakai, Risako, Tsuchiya, Toshiyuki, Tabata, Osamu, Kamei, Ken-Ichiro
• Format: Journal Article
• Language: English
• Published: England Nature Publishing Group 23.03.2023; Nature Publishing Group UK; Nature Portfolio
• Subjects: Animal models; Animals; Apoptosis; Biology; Caco-2 Cells; Cell lines; Endoplasmic reticulum; Fatty acids; Fatty liver; Gene expression; Hepatocytes; Humans; Lab-On-A-Chip Devices; Lipid Metabolism - genetics; Liver diseases; Microfluidics; Non-alcoholic Fatty Liver Disease - metabolism; Phenotypes
• ISSN: 2399-3642; 2399-3642
• DOI: 10.1038/s42003-023-04710-8

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.