Transcriptomic profiling of induced steatosis in mouse precision-cut liver slices

Progression of non-alcoholic fatty liver disease (NAFLD) to non-alcoholic steatohepatitis (NASH) is a major cause of end-stage liver diseases. There is a high need for predictive human ex vivo models to translate preclinical findings for potential new NAFLD drugs to human disease. About a decade ago, precision cut liver slices (PCLSs) have been established as an ex vivo assay for humans and other organisms. The molecular and functional baseline characteristics of PCLSs have been extensively described previously. In the present study, we provide a comprehensive RNA-Seq based molecular characterization of a new assay for NAFLD that induces steatosis in human and mouse PCLSs culture by incremental supplementation of sugars (glucose and fructose), insulin, and fatty acids (palmitate, oleate). Independent of the triglyceride levels of the human donor liver organs at baseline, the nutrient over-supplementation leads to an increase of triglyceride synthesis and cytokine release to the culture supernatant and thus recapitulates hallmark features of steatosis and inflammation in NAFLD. The mirrored design of human vs. mouse liver slices cultured at the exact same conditions allows a comprehensive assessment of donor variability and the contribution of time vs. nutrient factors to the overall observed molecular pattern and the investigation of conserved and species-specific transcriptional pathways that are involved in steatosis and inflammation of the liver. Animal Study Male C57/BL6 (Centrale Dienst Proefdieren, UMCG, Groningen, The Netherlands) were housed under standard conditions with chow and water ad libitum. Experiments were approved by the Animal Ethical Committee of the University of Groningen (Permit number 171290-01-001). At the time of sacrifice, mice were aged 10 weeks and their mean body weight was 26.4g. Livers were harvested after exsanguination under isoflurane/O2 anesthesia and stored in UW. Liver organs from five mice have been used for PCLS preparation. we incubated 48 PCLSs per animal (n=5), yielding a total of 80 samples. All mouse samples have been included. We prepared eight different media i.e. CTR: Control with 25mM Glucose, G: 36mM Glucose, F: 25mM Glucose + 5mM Fructose, GF: 36mM Glucose + 5mM Fructose, GFI: GF + 1nM Insulin, GFIO: GFI + 480uM Oleic acid, GIP: GFI + 240uM Palmitic acid, GFIPO: GFI + 480uM Oleic acid + 240uM Palmitic acid) and cultured PCLSs from each donor for 24h and 48h