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Hypoxia and HIF Signaling: One Axis with Divergent Effects

The correct concentration of oxygen in all tissues is a hallmark of cellular wellness, and the negative regulation of oxygen homeostasis is able to affect the cells and tissues of the whole organism. The cellular response to hypoxia is characterized by the activation of multiple genes involved in ma...

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Detalles Bibliográficos
Autores principales: Corrado, Chiara, Fontana, Simona
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7460602/
https://www.ncbi.nlm.nih.gov/pubmed/32764403
http://dx.doi.org/10.3390/ijms21165611
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author Corrado, Chiara
Fontana, Simona
author_facet Corrado, Chiara
Fontana, Simona
author_sort Corrado, Chiara
collection PubMed
description The correct concentration of oxygen in all tissues is a hallmark of cellular wellness, and the negative regulation of oxygen homeostasis is able to affect the cells and tissues of the whole organism. The cellular response to hypoxia is characterized by the activation of multiple genes involved in many biological processes. Among them, hypoxia-inducible factor (HIF) represents the master regulator of the hypoxia response. The active heterodimeric complex HIF α/β, binding to hypoxia-responsive elements (HREs), determines the induction of at least 100 target genes to restore tissue homeostasis. A growing body of evidence demonstrates that hypoxia signaling can act by generating contrasting responses in cells and tissues. Here, this dual and controversial role of hypoxia and the HIF signaling pathway is discussed, with particular reference to the effects induced on the complex activities of the immune system and on mechanisms determining cell and tissue responses after an injury in both acute and chronic human diseases related to the heart, lung, liver, and kidney.
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spelling pubmed-74606022020-09-03 Hypoxia and HIF Signaling: One Axis with Divergent Effects Corrado, Chiara Fontana, Simona Int J Mol Sci Review The correct concentration of oxygen in all tissues is a hallmark of cellular wellness, and the negative regulation of oxygen homeostasis is able to affect the cells and tissues of the whole organism. The cellular response to hypoxia is characterized by the activation of multiple genes involved in many biological processes. Among them, hypoxia-inducible factor (HIF) represents the master regulator of the hypoxia response. The active heterodimeric complex HIF α/β, binding to hypoxia-responsive elements (HREs), determines the induction of at least 100 target genes to restore tissue homeostasis. A growing body of evidence demonstrates that hypoxia signaling can act by generating contrasting responses in cells and tissues. Here, this dual and controversial role of hypoxia and the HIF signaling pathway is discussed, with particular reference to the effects induced on the complex activities of the immune system and on mechanisms determining cell and tissue responses after an injury in both acute and chronic human diseases related to the heart, lung, liver, and kidney. MDPI 2020-08-05 /pmc/articles/PMC7460602/ /pubmed/32764403 http://dx.doi.org/10.3390/ijms21165611 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
Corrado, Chiara
Fontana, Simona
Hypoxia and HIF Signaling: One Axis with Divergent Effects
title Hypoxia and HIF Signaling: One Axis with Divergent Effects
title_full Hypoxia and HIF Signaling: One Axis with Divergent Effects
title_fullStr Hypoxia and HIF Signaling: One Axis with Divergent Effects
title_full_unstemmed Hypoxia and HIF Signaling: One Axis with Divergent Effects
title_short Hypoxia and HIF Signaling: One Axis with Divergent Effects
title_sort hypoxia and hif signaling: one axis with divergent effects
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7460602/
https://www.ncbi.nlm.nih.gov/pubmed/32764403
http://dx.doi.org/10.3390/ijms21165611
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