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.
Nina GraffmannAudrey NcubeSoraia MartinsAurelian Robert FiszlPhilipp ReutherMartina BohndorfWasco WruckMathias BellerConstantin CzekeliusJames AdjayePublished in: Biology open (2021)
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.
Keyphrases
- high fat diet
- adipose tissue
- induced apoptosis
- insulin resistance
- induced pluripotent stem cells
- small molecule
- stem cells
- cell cycle arrest
- oxidative stress
- fatty acid
- endoplasmic reticulum stress
- high intensity
- cell death
- signaling pathway
- cell therapy
- gene expression
- genome wide
- cell proliferation
- copy number
- mesenchymal stem cells
- transcription factor
- heat stress