This study investigates the interplay between the PIDDosome complex and SCAP in regulating the progression from simple steatosis to steatohepatitis under a high-fructose diet. Using hepatocyte-specific Knockout mouse models for SCAP and PIDDosome components, the researchers demonstrate that SCAP ablation prevents simple steatosis but exacerbates ER stress and liver damage when combined with a high-fructose diet. Conversely, PIDDosome ablation reduces ER stress and protects against steatohepatitis, highlighting the antagonistic roles of these pathways in liver disease progression.
SCAP ablation inhibits simple steatosis but increases susceptibility to steatohepatitis under high-fructose diet due to enhanced ER stress. PIDDosome component ablation mitigates ER stress and protects against liver damage, suggesting potential therapeutic targets for preventing NASH progression.
Hepatocyte-specific SCAP Knockout (Scap^ΔHep) and PIDDosome component Knockouts (e.g., Casp2^−/−, Pidd1^−/−)
Non-alcoholic fatty liver disease (NAFLD), Non-alcoholic steatohepatitis (NASH), ER stress, Lipid metabolism, Hepatic inflammation
Conditional Knockout models, Hepatocyte-specific gene deletion, Albumin-Cre driver, High-fructose diet-induced liver disease, ER stress modulation
From model design to experimental results
Featured in 600+ scientific articles
Collaboration with 17 Top Pharmas,
170+ Biotechs and 380+ Academic Institutions
Generated with biopharma partners and in-house
and guaranteed freedom to operate
Models with certified health status from professional breeders in US and Europe
