In Vitro Fatty Liver (Steatosis) 2D/3D Research Models



Model Overview


In vitro fatty liver models replicate hepatic steatosis—a condition characterized by excessive lipid accumulation in hepatocytes—using 2D monolayer cultures or 3D multicellular systems. These models are critical for studying disease mechanisms, drug-induced lipid toxicity, and therapeutic interventions for non-alcoholic fatty liver disease (NAFLD) or alcoholic fatty liver disease (AFLD).


1. 2D Steatosis Models

  • Construction:

    • Primary hepatocytes or hepatoma cell lines (e.g., HepG2, Huh7) are exposed to free fatty acids (FFA, e.g., palmitate/oleate) or ethanol to induce lipid droplet formation.

  • Applications:

    • High-throughput screening of anti-steatotic compounds.

    • Mechanistic studies of lipid metabolism dysregulation (e.g., PPAR-γ, SREBP-1c pathways).

  • Advantages:

    • Simple, cost-effective, and scalable for rapid toxicity/efficacy assessments.


2. 3D Steatosis Models

  • Construction:

    • Co-culture hepatocytes with stellate cellsKupffer cells, and endothelial cells in 3D spheroids or organoids under lipid/ethanol stimulation.

    • Incorporate extracellular matrix (ECM) to mimic fibrotic progression in advanced NAFLD.

  • Applications:

    • Study cell-cell interactions driving inflammation and fibrosis.

    • Evaluate drug penetration and efficacy in a physiologically relevant microenvironment.

  • Advantages:

    • Recapitulate lipid accumulationoxidative stress, and immune activation observed in vivo.

    • Support long-term studies of chronic steatosis-to-NASH transition.


Key Features

  • Pathological Hallmarks:

    • Lipid droplet quantification (Oil Red O staining, BODIPY probes).

    • Inflammation biomarkers (TNF-α, IL-6) and fibrosis markers (α-SMA, collagen deposition).

  • Functional Readouts:

    • Mitochondrial dysfunction (ROS, ATP levels).

    • Insulin resistance (glucose uptake assays).


Technical Capabilities

  • Customizable Models:

    • Species-specific (human, mouse, rat) or disease-stage-specific (simple steatosis vs. NASH).

    • Integration with microfluidic chips for dynamic nutrient/drug perfusion.

  • Analytical Platforms:

    • High-content imaging, lipidomics, and transcriptomic profiling.


Why Choose Our Models?

Developed by a team with 14+ years of liver research expertise, our steatosis models bridge the gap between simplistic cell cultures and complex in vivo systems, delivering human-relevant data to accelerate drug discovery and mechanistic research.