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The Factor Inhibiting HIF Asparaginyl Hydroxylase Regulates Oxidative Metabolism and Accelerates Metabolic Adaptation to Hypoxia

Animals require an immediate response to oxygen availability to allow rapid shifts between oxidative and glycolytic metabolism. These metabolic shifts are highly regulated by the HIF transcription factor. The factor inhibiting HIF (FIH) is an asparaginyl hydroxylase that controls HIF transcriptional...

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Autores principales: Sim, Jingwei, Cowburn, Andrew S., Palazon, Asis, Madhu, Basetti, Tyrakis, Petros A., Macías, David, Bargiela, David M., Pietsch, Sandra, Gralla, Michael, Evans, Colin E., Kittipassorn, Thaksaon, Chey, Yu C.J., Branco, Cristina M., Rundqvist, Helene, Peet, Daniel J., Johnson, Randall S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5887987/
https://www.ncbi.nlm.nih.gov/pubmed/29617647
http://dx.doi.org/10.1016/j.cmet.2018.02.020
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author Sim, Jingwei
Cowburn, Andrew S.
Palazon, Asis
Madhu, Basetti
Tyrakis, Petros A.
Macías, David
Bargiela, David M.
Pietsch, Sandra
Gralla, Michael
Evans, Colin E.
Kittipassorn, Thaksaon
Chey, Yu C.J.
Branco, Cristina M.
Rundqvist, Helene
Peet, Daniel J.
Johnson, Randall S.
author_facet Sim, Jingwei
Cowburn, Andrew S.
Palazon, Asis
Madhu, Basetti
Tyrakis, Petros A.
Macías, David
Bargiela, David M.
Pietsch, Sandra
Gralla, Michael
Evans, Colin E.
Kittipassorn, Thaksaon
Chey, Yu C.J.
Branco, Cristina M.
Rundqvist, Helene
Peet, Daniel J.
Johnson, Randall S.
author_sort Sim, Jingwei
collection PubMed
description Animals require an immediate response to oxygen availability to allow rapid shifts between oxidative and glycolytic metabolism. These metabolic shifts are highly regulated by the HIF transcription factor. The factor inhibiting HIF (FIH) is an asparaginyl hydroxylase that controls HIF transcriptional activity in an oxygen-dependent manner. We show here that FIH loss increases oxidative metabolism, while also increasing glycolytic capacity, and that this gives rise to an increase in oxygen consumption. We further show that the loss of FIH acts to accelerate the cellular metabolic response to hypoxia. Skeletal muscle expresses 50-fold higher levels of FIH than other tissues: we analyzed skeletal muscle FIH mutants and found a decreased metabolic efficiency, correlated with an increased oxidative rate and an increased rate of hypoxic response. We find that FIH, through its regulation of oxidation, acts in concert with the PHD/vHL pathway to accelerate HIF-mediated metabolic responses to hypoxia.
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spelling pubmed-58879872018-04-06 The Factor Inhibiting HIF Asparaginyl Hydroxylase Regulates Oxidative Metabolism and Accelerates Metabolic Adaptation to Hypoxia Sim, Jingwei Cowburn, Andrew S. Palazon, Asis Madhu, Basetti Tyrakis, Petros A. Macías, David Bargiela, David M. Pietsch, Sandra Gralla, Michael Evans, Colin E. Kittipassorn, Thaksaon Chey, Yu C.J. Branco, Cristina M. Rundqvist, Helene Peet, Daniel J. Johnson, Randall S. Cell Metab Article Animals require an immediate response to oxygen availability to allow rapid shifts between oxidative and glycolytic metabolism. These metabolic shifts are highly regulated by the HIF transcription factor. The factor inhibiting HIF (FIH) is an asparaginyl hydroxylase that controls HIF transcriptional activity in an oxygen-dependent manner. We show here that FIH loss increases oxidative metabolism, while also increasing glycolytic capacity, and that this gives rise to an increase in oxygen consumption. We further show that the loss of FIH acts to accelerate the cellular metabolic response to hypoxia. Skeletal muscle expresses 50-fold higher levels of FIH than other tissues: we analyzed skeletal muscle FIH mutants and found a decreased metabolic efficiency, correlated with an increased oxidative rate and an increased rate of hypoxic response. We find that FIH, through its regulation of oxidation, acts in concert with the PHD/vHL pathway to accelerate HIF-mediated metabolic responses to hypoxia. Cell Press 2018-04-03 /pmc/articles/PMC5887987/ /pubmed/29617647 http://dx.doi.org/10.1016/j.cmet.2018.02.020 Text en © 2018 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sim, Jingwei
Cowburn, Andrew S.
Palazon, Asis
Madhu, Basetti
Tyrakis, Petros A.
Macías, David
Bargiela, David M.
Pietsch, Sandra
Gralla, Michael
Evans, Colin E.
Kittipassorn, Thaksaon
Chey, Yu C.J.
Branco, Cristina M.
Rundqvist, Helene
Peet, Daniel J.
Johnson, Randall S.
The Factor Inhibiting HIF Asparaginyl Hydroxylase Regulates Oxidative Metabolism and Accelerates Metabolic Adaptation to Hypoxia
title The Factor Inhibiting HIF Asparaginyl Hydroxylase Regulates Oxidative Metabolism and Accelerates Metabolic Adaptation to Hypoxia
title_full The Factor Inhibiting HIF Asparaginyl Hydroxylase Regulates Oxidative Metabolism and Accelerates Metabolic Adaptation to Hypoxia
title_fullStr The Factor Inhibiting HIF Asparaginyl Hydroxylase Regulates Oxidative Metabolism and Accelerates Metabolic Adaptation to Hypoxia
title_full_unstemmed The Factor Inhibiting HIF Asparaginyl Hydroxylase Regulates Oxidative Metabolism and Accelerates Metabolic Adaptation to Hypoxia
title_short The Factor Inhibiting HIF Asparaginyl Hydroxylase Regulates Oxidative Metabolism and Accelerates Metabolic Adaptation to Hypoxia
title_sort factor inhibiting hif asparaginyl hydroxylase regulates oxidative metabolism and accelerates metabolic adaptation to hypoxia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5887987/
https://www.ncbi.nlm.nih.gov/pubmed/29617647
http://dx.doi.org/10.1016/j.cmet.2018.02.020
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