scholarly journals Critical role of charged residues in helix 7 of the ligand binding domain in Hepatocyte Nuclear Factor 4  dimerisation and transcriptional activity

2003 ◽  
Vol 31 (22) ◽  
pp. 6640-6650 ◽  
Author(s):  
J. Eeckhoute
Keyword(s):  
Ligand Binding ◽  
Transcriptional Activity ◽  
Critical Role ◽  
Binding Domain ◽  
Ligand Binding Domain ◽  
Nuclear Factor ◽  
Hepatocyte Nuclear Factor ◽  
Charged Residues ◽  
Hepatocyte Nuclear Factor 4

scholarly journals Critical Role of Residues Defining the Ligand Binding Pocket in Hepatocyte Nuclear Factor-4α

2004 ◽  
Vol 279 (29) ◽  
pp. 30680-30688 ◽  
Author(s):  
Eleni Aggelidou ◽  
Panagiota Iordanidou ◽  
Panayota Tsantili ◽  
Georgios Papadopoulos ◽  
Margarita Hadzopoulou-Cladaras
Keyword(s):  
Ligand Binding ◽  
Critical Role ◽  
Binding Pocket ◽  
Nuclear Factor ◽  
Hepatocyte Nuclear Factor ◽  
Ligand Binding Pocket ◽  
Hepatocyte Nuclear Factor 4Α

Solution Structure of the Ligand Binding Domain of the Fibroblast Growth Factor Receptor:  Role of Heparin in the Activation of the Receptor†,‡

Biochemistry ◽  
2005 ◽  
Vol 44 (48) ◽  
pp. 15787-15798 ◽  
Author(s):  
Kuo-Wei Hung ◽  
Thallapuranam Krishnaswamy S. Kumar ◽  
Karuppanan Muthusamy Kathir ◽  
Ping Xu ◽  
Feng Ni ◽  
...  
Keyword(s):  
Growth Factor ◽  
Ligand Binding ◽  
Fibroblast Growth Factor ◽  
Solution Structure ◽  
Fibroblast Growth Factor Receptor ◽  
Growth Factor Receptor ◽  
Binding Domain ◽  
Ligand Binding Domain ◽  
Fibroblast Growth

scholarly journals Hepatocyte Nuclear Factor 4 alpha (HNF4α) Activation is Essential for Termination of Liver Regeneration

2018 ◽  
Author(s):  
Ian Huck ◽  
Sumedha Gunewardena ◽  
Regina Espanol-Suner ◽  
Holger Willenbring ◽  
Udayan Apte
Keyword(s):  
Gene Expression ◽  
Liver Regeneration ◽  
Target Gene ◽  
Nuclear Factor ◽  
Hepatocyte Nuclear Factor ◽  
Hepatic Differentiation ◽  
Target Gene Expression ◽  
Protein Levels ◽  
Hepatocyte Nuclear Factor 4

AbstractHepatocyte Nuclear Factor 4 alpha (HNF4α) is critical for hepatic differentiation. Recent studies have highlighted its role in inhibition of hepatocyte proliferation and tumor suppression. However, the role of HNF4α in liver regeneration is not known. We hypothesized that hepatocytes modulate HNF4α activity when navigating between differentiated and proliferative states during liver regeneration. Western blot analysis revealed a rapid decline in nuclear and cytoplasmic HNF4α protein levels accompanied with decreased target gene expression within 1 hour after 2/3 partial hepatectomy (post-PH) in C57BL/6J mice. HNF4α protein expression did not recover to the pre-PH levels until day 3. Hepatocyte-specific deletion of HNF4α (HNF4α-KO) in mice resulted in 100% mortality post-PH despite increased proliferative marker expression throughout regeneration. Sustained loss of HNF4α target gene expression throughout regeneration indicated HNF4α-KO mice were unable to compensate for loss of HNF4α transcriptional activity. Deletion of HNF4α resulted in sustained proliferation accompanied by c-myc and cyclin D1 over expression and a complete deficiency of hepatocyte function after PH. Interestingly, overexpression of degradation-resistant HNF4α in hepatocytes did not prevent initiation of regeneration after PH. Finally, AAV8-mediated reexpression of HNF4α in hepatocytes of HNF4α-KO mice post-PH restored HNF4α protein levels, induced target gene expression and improved survival of HNF4α-KO mice post-PH. In conclusion, these data indicate that HNF4α reexpression following initial decrease is critical for hepatocytes to exit from cell cycle and resume function during the termination phase of liver regeneration. These results reveal the role of HNF4α in liver regeneration and have implications for therapy of liver failure.

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