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Control of Cell Identity by the Nuclear Receptor HNF4 in Organ Pathophysiology

Hepatocyte Nuclear Factor 4 (HNF4) is a transcription factor (TF) belonging to the nuclear receptor family whose expression and activities are restricted to a limited number of organs including the liver and gastrointestinal tract. In this review, we present robust evidence pointing to HNF4 as a mas...

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Autores principales: Dubois, Vanessa, Staels, Bart, Lefebvre, Philippe, Verzi, Michael P., Eeckhoute, Jérôme
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7600215/
https://www.ncbi.nlm.nih.gov/pubmed/32998360
http://dx.doi.org/10.3390/cells9102185
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author Dubois, Vanessa
Staels, Bart
Lefebvre, Philippe
Verzi, Michael P.
Eeckhoute, Jérôme
author_facet Dubois, Vanessa
Staels, Bart
Lefebvre, Philippe
Verzi, Michael P.
Eeckhoute, Jérôme
author_sort Dubois, Vanessa
collection PubMed
description Hepatocyte Nuclear Factor 4 (HNF4) is a transcription factor (TF) belonging to the nuclear receptor family whose expression and activities are restricted to a limited number of organs including the liver and gastrointestinal tract. In this review, we present robust evidence pointing to HNF4 as a master regulator of cellular differentiation during development and a safekeeper of acquired cell identity in adult organs. Importantly, we discuss that transient loss of HNF4 may represent a protective mechanism upon acute organ injury, while prolonged impairment of HNF4 activities could contribute to organ dysfunction. In this context, we describe in detail mechanisms involved in the pathophysiological control of cell identity by HNF4, including how HNF4 works as part of cell-specific TF networks and how its expression/activities are disrupted in injured organs.
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spelling pubmed-76002152020-11-01 Control of Cell Identity by the Nuclear Receptor HNF4 in Organ Pathophysiology Dubois, Vanessa Staels, Bart Lefebvre, Philippe Verzi, Michael P. Eeckhoute, Jérôme Cells Review Hepatocyte Nuclear Factor 4 (HNF4) is a transcription factor (TF) belonging to the nuclear receptor family whose expression and activities are restricted to a limited number of organs including the liver and gastrointestinal tract. In this review, we present robust evidence pointing to HNF4 as a master regulator of cellular differentiation during development and a safekeeper of acquired cell identity in adult organs. Importantly, we discuss that transient loss of HNF4 may represent a protective mechanism upon acute organ injury, while prolonged impairment of HNF4 activities could contribute to organ dysfunction. In this context, we describe in detail mechanisms involved in the pathophysiological control of cell identity by HNF4, including how HNF4 works as part of cell-specific TF networks and how its expression/activities are disrupted in injured organs. MDPI 2020-09-28 /pmc/articles/PMC7600215/ /pubmed/32998360 http://dx.doi.org/10.3390/cells9102185 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Dubois, Vanessa
Staels, Bart
Lefebvre, Philippe
Verzi, Michael P.
Eeckhoute, Jérôme
Control of Cell Identity by the Nuclear Receptor HNF4 in Organ Pathophysiology
title Control of Cell Identity by the Nuclear Receptor HNF4 in Organ Pathophysiology
title_full Control of Cell Identity by the Nuclear Receptor HNF4 in Organ Pathophysiology
title_fullStr Control of Cell Identity by the Nuclear Receptor HNF4 in Organ Pathophysiology
title_full_unstemmed Control of Cell Identity by the Nuclear Receptor HNF4 in Organ Pathophysiology
title_short Control of Cell Identity by the Nuclear Receptor HNF4 in Organ Pathophysiology
title_sort control of cell identity by the nuclear receptor hnf4 in organ pathophysiology
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7600215/
https://www.ncbi.nlm.nih.gov/pubmed/32998360
http://dx.doi.org/10.3390/cells9102185
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