AI Article Synopsis

  • Non-alcoholic fatty liver disease (NAFLD) affects many people, but effective treatments are lacking due to limitations in current research methods.
  • The study introduces an integrated-gut-liver-on-a-chip (iGLC) system that simulates human gut-liver interactions by co-culturing gut and liver cell lines in a microfluidic environment, allowing for observation of NAFLD development.
  • Results show that gut-liver co-cultured cells can protect against fat-induced cell death, while providing insights into lipid accumulation and gene expression changes linked to cellular stress, suggesting the iGLC platform could replace animal testing for studying NAFLD.

Article Abstract

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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10036655PMC
http://dx.doi.org/10.1038/s42003-023-04710-8DOI Listing

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