Hepatocyte-specific deletion of hepatocyte nuclear factor-4α in adult mice results in increased hepatocyte proliferation

• DOI: 10.1152/ajpgi.00064.2012
• Publication Date: 2012-10-27T00:51:23Z
• Authors: Chad Walesky; Sumedha Gunewardena; Ernest F. Terwill...; Genea Edwards; Prachi Borude; Udayan Apte
• Keywords: Mice, Knockout; Chromatin Immunoprecipitation; 0303 health sciences; Blotting, Western; Cell Cycle; Fluorescent Antibody Technique; Mitosis; Dependovirus; Flow Cytometry; Microarray Analysis; Real-Time Polymerase Chain Reaction; Immunohistochemistry; Cell Line; Liver Regeneration; 3. Good health; Mice; 03 medical and health sciences; Hepatocyte Nuclear Factor 4; Capillary Electrochromatography; Hepatocytes; Animals; Gene Deletion; Cell Proliferation

Hepatocyte nuclear factor-4α (HNF4α) is known as the master regulator of hepatocyte differentiation. Recent studies indicate that HNF4α may inhibit hepatocyte proliferation via mechanisms that have yet to be identified. Using a HNF4α knockdown mouse model based on delivery of inducible Cre recombinase via an adeno-associated virus 8 viral vector, we investigated the role of HNF4α in the regulation of hepatocyte proliferation. Hepatocyte-specific deletion of HNF4α resulted in increased hepatocyte proliferation. Global gene expression analysis showed that a majority of the downregulated genes were previously known HNF4α target genes involved in hepatic differentiation. Interestingly, ≥500 upregulated genes were associated with cell proliferation and cancer. Furthermore, we identified potential negative target genes of HNF4α, many of which are involved in the stimulation of proliferation. Using chromatin immunoprecipitation analysis, we confirmed binding of HNF4α at three of these genes. Furthermore, overexpression of HNF4α in mouse hepatocellular carcinoma cells resulted in a decrease in promitogenic gene expression and cell cycle arrest. Taken together, these data indicate that, apart from its role in hepatocyte differentiation, HNF4α actively inhibits hepatocyte proliferation by repression of specific promitogenic genes.