Role of HNF4α-cMyc Interaction in CDE Diet-Induced Liver Injury and Regeneration.

Am J Pathol

Department of Pharmacology, Toxicology, and Therapeutics, University of Kansas Medical Center, Kansas City, Kansas. Electronic address:

Published: July 2024

AI Article Synopsis

  • HNF4α is crucial for liver function and helps regulate cMyc, affecting liver injury and regeneration.
  • The study used different mouse models to investigate the effects of HNF4α and cMyc on liver damage caused by a CDE diet, showing that HNF4α deletion led to increased liver injury.
  • Results indicated that while HNF4α protects the liver from inflammation and fibrosis, the absence of cMyc resulted in reduced liver injury, suggesting HNF4α's protective role is influenced by cMyc.

Article Abstract

Hepatocyte nuclear factor 4 alpha (HNF4α) is a nuclear factor essential for liver function that regulates the expression of cMyc and plays an important role during liver regeneration. This study investigated the role of the HNF4α-cMyc interaction in regulating liver injury and regeneration using the choline-deficient and ethionine-supplemented (CDE) diet model. Wild-type (WT), hepatocyte-specific HNF4α-knockout (KO), cMyc-KO, and HNF4α-cMyc double KO (DKO) mice were fed a CDE diet for 1 week to induce subacute liver injury. To study regeneration, normal chow diet was fed for 1 week after CDE diet. WT mice exhibited significant liver injury and decreased HNF4α mRNA and protein expression after CDE diet. HNF4α deletion resulted in significantly higher injury with increased inflammation, fibrosis, proliferation, and hepatic progenitor cell activation compared with WT mice after CDE diet but indicated similar recovery. Deletion of cMyc lowered liver injury with activation of inflammatory genes compared with WT and HNF4α-KO mice after CDE diet. DKO mice had a phenotype comparable to that of the HNF4α-KO mice after CDE diet and a complete recovery. DKO mice exhibited a significant increase in hepatic progenitor cell markers both after injury and recovery phase. Taken together, these data show that HNF4α protects against inflammatory and fibrotic changes after CDE diet-induced injury, which is driven by cMyc.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11317903PMC
http://dx.doi.org/10.1016/j.ajpath.2024.03.008DOI Listing

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