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NCOA4-Mediated Ferritinophagy: A Potential Link to Neurodegeneration

NCOA4 (Nuclear receptor coactivator 4) mediates the selective autophagic degradation of ferritin, the cellular cytosolic iron storage complex, thereby playing a critical role in intracellular and systemic iron homeostasis. Disruptions in iron homeostasis and autophagy are observed in several neurode...

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Detalles Bibliográficos
Autores principales: Quiles del Rey, Maria, Mancias, Joseph D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6427834/
https://www.ncbi.nlm.nih.gov/pubmed/30930742
http://dx.doi.org/10.3389/fnins.2019.00238
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author Quiles del Rey, Maria
Mancias, Joseph D.
author_facet Quiles del Rey, Maria
Mancias, Joseph D.
author_sort Quiles del Rey, Maria
collection PubMed
description NCOA4 (Nuclear receptor coactivator 4) mediates the selective autophagic degradation of ferritin, the cellular cytosolic iron storage complex, thereby playing a critical role in intracellular and systemic iron homeostasis. Disruptions in iron homeostasis and autophagy are observed in several neurodegenerative disorders raising the possibility that NCOA4-mediated ferritinophagy links these two observations and may underlie, in part, the pathophysiology of neurodegeneration. Here, we review the available evidence detailing the molecular mechanisms of NCOA4-mediated ferritinophagy and recent studies examining its role in systemic iron homeostasis and erythropoiesis. We propose additional studies to examine the potential role of NCOA4 in the brain in the context of neurodegenerative diseases.
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spelling pubmed-64278342019-03-29 NCOA4-Mediated Ferritinophagy: A Potential Link to Neurodegeneration Quiles del Rey, Maria Mancias, Joseph D. Front Neurosci Neuroscience NCOA4 (Nuclear receptor coactivator 4) mediates the selective autophagic degradation of ferritin, the cellular cytosolic iron storage complex, thereby playing a critical role in intracellular and systemic iron homeostasis. Disruptions in iron homeostasis and autophagy are observed in several neurodegenerative disorders raising the possibility that NCOA4-mediated ferritinophagy links these two observations and may underlie, in part, the pathophysiology of neurodegeneration. Here, we review the available evidence detailing the molecular mechanisms of NCOA4-mediated ferritinophagy and recent studies examining its role in systemic iron homeostasis and erythropoiesis. We propose additional studies to examine the potential role of NCOA4 in the brain in the context of neurodegenerative diseases. Frontiers Media S.A. 2019-03-14 /pmc/articles/PMC6427834/ /pubmed/30930742 http://dx.doi.org/10.3389/fnins.2019.00238 Text en Copyright © 2019 Quiles del Rey and Mancias. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Quiles del Rey, Maria
Mancias, Joseph D.
NCOA4-Mediated Ferritinophagy: A Potential Link to Neurodegeneration
title NCOA4-Mediated Ferritinophagy: A Potential Link to Neurodegeneration
title_full NCOA4-Mediated Ferritinophagy: A Potential Link to Neurodegeneration
title_fullStr NCOA4-Mediated Ferritinophagy: A Potential Link to Neurodegeneration
title_full_unstemmed NCOA4-Mediated Ferritinophagy: A Potential Link to Neurodegeneration
title_short NCOA4-Mediated Ferritinophagy: A Potential Link to Neurodegeneration
title_sort ncoa4-mediated ferritinophagy: a potential link to neurodegeneration
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6427834/
https://www.ncbi.nlm.nih.gov/pubmed/30930742
http://dx.doi.org/10.3389/fnins.2019.00238
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