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

Hepatocyte 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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Hepatology (Baltimore, Md.) Md.), 2019-03, Vol.70 (2), p.666-681
Hauptverfasser: Huck, Ian, Gunewardena, Sumedha, Espanol-Suner, Regina, Willenbring, Holger, Apte, Udayan
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 681
container_issue 2
container_start_page 666
container_title Hepatology (Baltimore, Md.)
container_volume 70
creator Huck, Ian
Gunewardena, Sumedha
Espanol-Suner, Regina
Willenbring, Holger
Apte, Udayan
description Hepatocyte 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 delayed but 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.
doi_str_mv 10.1002/hep.30405
format Article
fullrecord <record><control><sourceid>pubmedcentral</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6551324</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>pubmedcentral_primary_oai_pubmedcentral_nih_gov_6551324</sourcerecordid><originalsourceid>FETCH-pubmedcentral_primary_oai_pubmedcentral_nih_gov_65513243</originalsourceid><addsrcrecordid>eNqljM1Kw0AURgdRbPxZ-AZ3qYvUm_lpzUYQachCupDuwzXeNCNJJsxMA30sX8RnslQ3rl198J3DEeImw3mGKO9bHucKNZoTkWRGLlOlDJ6KBOUS0zxT-UxchPCBiLmWD-diptBIxIVMRFvySNHV-8iw3tUdk4eC6ug8aKBubAluy3Whvz7v4KmOdqJo3QA2wCoEHqKlDpqDvGHf2-EHugZe7MQeXnnLA_vjeyXOGuoCX__upXgsVpvnMh13bz2_14eWp64ave3J7ytHtvpLBttWWzdVC2MyJbX6d-AbkYhlaQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Hepatocyte Nuclear Factor 4 alpha (HNF4α) Activation is Essential for Termination of Liver Regeneration</title><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Access via Wiley Online Library</source><creator>Huck, Ian ; Gunewardena, Sumedha ; Espanol-Suner, Regina ; Willenbring, Holger ; Apte, Udayan</creator><creatorcontrib>Huck, Ian ; Gunewardena, Sumedha ; Espanol-Suner, Regina ; Willenbring, Holger ; Apte, Udayan</creatorcontrib><description>Hepatocyte 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 delayed but 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.</description><identifier>ISSN: 0270-9139</identifier><identifier>EISSN: 1527-3350</identifier><identifier>DOI: 10.1002/hep.30405</identifier><identifier>PMID: 30520062</identifier><language>eng</language><ispartof>Hepatology (Baltimore, Md.), 2019-03, Vol.70 (2), p.666-681</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,315,781,785,886,27929,27930</link.rule.ids></links><search><creatorcontrib>Huck, Ian</creatorcontrib><creatorcontrib>Gunewardena, Sumedha</creatorcontrib><creatorcontrib>Espanol-Suner, Regina</creatorcontrib><creatorcontrib>Willenbring, Holger</creatorcontrib><creatorcontrib>Apte, Udayan</creatorcontrib><title>Hepatocyte Nuclear Factor 4 alpha (HNF4α) Activation is Essential for Termination of Liver Regeneration</title><title>Hepatology (Baltimore, Md.)</title><description>Hepatocyte 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 delayed but 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.</description><issn>0270-9139</issn><issn>1527-3350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNqljM1Kw0AURgdRbPxZ-AZ3qYvUm_lpzUYQachCupDuwzXeNCNJJsxMA30sX8RnslQ3rl198J3DEeImw3mGKO9bHucKNZoTkWRGLlOlDJ6KBOUS0zxT-UxchPCBiLmWD-diptBIxIVMRFvySNHV-8iw3tUdk4eC6ug8aKBubAluy3Whvz7v4KmOdqJo3QA2wCoEHqKlDpqDvGHf2-EHugZe7MQeXnnLA_vjeyXOGuoCX__upXgsVpvnMh13bz2_14eWp64ave3J7ytHtvpLBttWWzdVC2MyJbX6d-AbkYhlaQ</recordid><startdate>20190310</startdate><enddate>20190310</enddate><creator>Huck, Ian</creator><creator>Gunewardena, Sumedha</creator><creator>Espanol-Suner, Regina</creator><creator>Willenbring, Holger</creator><creator>Apte, Udayan</creator><scope>5PM</scope></search><sort><creationdate>20190310</creationdate><title>Hepatocyte Nuclear Factor 4 alpha (HNF4α) Activation is Essential for Termination of Liver Regeneration</title><author>Huck, Ian ; Gunewardena, Sumedha ; Espanol-Suner, Regina ; Willenbring, Holger ; Apte, Udayan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-pubmedcentral_primary_oai_pubmedcentral_nih_gov_65513243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Huck, Ian</creatorcontrib><creatorcontrib>Gunewardena, Sumedha</creatorcontrib><creatorcontrib>Espanol-Suner, Regina</creatorcontrib><creatorcontrib>Willenbring, Holger</creatorcontrib><creatorcontrib>Apte, Udayan</creatorcontrib><collection>PubMed Central (Full Participant titles)</collection><jtitle>Hepatology (Baltimore, Md.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Huck, Ian</au><au>Gunewardena, Sumedha</au><au>Espanol-Suner, Regina</au><au>Willenbring, Holger</au><au>Apte, Udayan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hepatocyte Nuclear Factor 4 alpha (HNF4α) Activation is Essential for Termination of Liver Regeneration</atitle><jtitle>Hepatology (Baltimore, Md.)</jtitle><date>2019-03-10</date><risdate>2019</risdate><volume>70</volume><issue>2</issue><spage>666</spage><epage>681</epage><pages>666-681</pages><issn>0270-9139</issn><eissn>1527-3350</eissn><abstract>Hepatocyte 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 delayed but 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.</abstract><pmid>30520062</pmid><doi>10.1002/hep.30405</doi></addata></record>
fulltext fulltext
identifier ISSN: 0270-9139
ispartof Hepatology (Baltimore, Md.), 2019-03, Vol.70 (2), p.666-681
issn 0270-9139
1527-3350
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6551324
source Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Access via Wiley Online Library
title Hepatocyte Nuclear Factor 4 alpha (HNF4α) Activation is Essential for Termination of Liver Regeneration
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-09T19%3A53%3A35IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmedcentral&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Hepatocyte%20Nuclear%20Factor%204%20alpha%20(HNF4%CE%B1)%20Activation%20is%20Essential%20for%20Termination%20of%20Liver%20Regeneration&rft.jtitle=Hepatology%20(Baltimore,%20Md.)&rft.au=Huck,%20Ian&rft.date=2019-03-10&rft.volume=70&rft.issue=2&rft.spage=666&rft.epage=681&rft.pages=666-681&rft.issn=0270-9139&rft.eissn=1527-3350&rft_id=info:doi/10.1002/hep.30405&rft_dat=%3Cpubmedcentral%3Epubmedcentral_primary_oai_pubmedcentral_nih_gov_6551324%3C/pubmedcentral%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/30520062&rfr_iscdi=true