Neuronal development is promoted by weakened intrinsic antioxidant defences due to epigenetic repression of Nrf2

Forebrain neurons have weak intrinsic antioxidant defences compared with astrocytes, but the molecular basis and purpose of this is poorly understood. We show that early in mouse cortical neuronal development in vitro and in vivo , expression of the master-regulator of antioxidant genes, transcripti...

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Published inNature communications Vol. 6; no. 1; p. 7066
Main Authors Bell, Karen F.S., Al-Mubarak, Bashayer, Martel, Marc-André, McKay, Sean, Wheelan, Nicola, Hasel, Philip, Márkus, Nóra M., Baxter, Paul, Deighton, Ruth F., Serio, Andrea, Bilican, Bilada, Chowdhry, Sudhir, Meakin, Paul J., Ashford, Michael L.J., Wyllie, David J.A., Scannevin, Robert H., Chandran, Siddharthan, Hayes, John D., Hardingham, Giles E.
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 13.05.2015
Nature Publishing Group
Nature Pub. Group
Subjects
Online AccessGet full text
ISSN2041-1723
2041-1723
DOI10.1038/ncomms8066

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Abstract Forebrain neurons have weak intrinsic antioxidant defences compared with astrocytes, but the molecular basis and purpose of this is poorly understood. We show that early in mouse cortical neuronal development in vitro and in vivo , expression of the master-regulator of antioxidant genes, transcription factor NF-E2-related-factor-2 (Nrf2), is repressed by epigenetic inactivation of its promoter. Consequently, in contrast to astrocytes or young neurons, maturing neurons possess negligible Nrf2-dependent antioxidant defences, and exhibit no transcriptional responses to Nrf2 activators, or to ablation of Nrf2’s inhibitor Keap1. Neuronal Nrf2 inactivation seems to be required for proper development: in maturing neurons, ectopic Nrf2 expression inhibits neurite outgrowth and aborization, and electrophysiological maturation, including synaptogenesis. These defects arise because Nrf2 activity buffers neuronal redox status, inhibiting maturation processes dependent on redox-sensitive JNK and Wnt pathways. Thus, developmental epigenetic Nrf2 repression weakens neuronal antioxidant defences but is necessary to create an environment that supports neuronal development. Neurons in the brain are more susceptible to oxidative stress than astroglial cells but the molecular basis and biological reasons for this are poorly understood. Here the authors show that developing cortical neurons have reduced levels of the antioxidant transcription factor Nrf2 due to epigenetic silencing and that this is necessary for proper neuronal development.
AbstractList Forebrain neurons have weak intrinsic antioxidant defences compared with astrocytes, but the molecular basis and purpose of this is poorly understood. We show that early in mouse cortical neuronal development in vitro and in vivo, expression of the master-regulator of antioxidant genes, transcription factor NF-E2-related-factor-2 (Nrf2), is repressed by epigenetic inactivation of its promoter. Consequently, in contrast to astrocytes or young neurons, maturing neurons possess negligible Nrf2-dependent antioxidant defences, and exhibit no transcriptional responses to Nrf2 activators, or to ablation of Nrf2's inhibitor Keap1. Neuronal Nrf2 inactivation seems to be required for proper development: in maturing neurons, ectopic Nrf2 expression inhibits neurite outgrowth and aborization, and electrophysiological maturation, including synaptogenesis. These defects arise because Nrf2 activity buffers neuronal redox status, inhibiting maturation processes dependent on redox-sensitive JNK and Wnt pathways. Thus, developmental epigenetic Nrf2 repression weakens neuronal antioxidant defences but is necessary to create an environment that supports neuronal development.
Forebrain neurons have weak intrinsic antioxidant defences compared with astrocytes, but the molecular basis and purpose of this is poorly understood. We show that early in mouse cortical neuronal development in vitro and in vivo , expression of the master-regulator of antioxidant genes, transcription factor NF-E2-related-factor-2 (Nrf2), is repressed by epigenetic inactivation of its promoter. Consequently, in contrast to astrocytes or young neurons, maturing neurons possess negligible Nrf2-dependent antioxidant defences, and exhibit no transcriptional responses to Nrf2 activators, or to ablation of Nrf2’s inhibitor Keap1. Neuronal Nrf2 inactivation seems to be required for proper development: in maturing neurons, ectopic Nrf2 expression inhibits neurite outgrowth and aborization, and electrophysiological maturation, including synaptogenesis. These defects arise because Nrf2 activity buffers neuronal redox status, inhibiting maturation processes dependent on redox-sensitive JNK and Wnt pathways. Thus, developmental epigenetic Nrf2 repression weakens neuronal antioxidant defences but is necessary to create an environment that supports neuronal development. Neurons in the brain are more susceptible to oxidative stress than astroglial cells but the molecular basis and biological reasons for this are poorly understood. Here the authors show that developing cortical neurons have reduced levels of the antioxidant transcription factor Nrf2 due to epigenetic silencing and that this is necessary for proper neuronal development.
Forebrain neurons have weak intrinsic antioxidant defences compared with astrocytes, but the molecular basis and purpose of this is poorly understood. We show that early in mouse cortical neuronal development in vitro and in vivo , expression of the master-regulator of antioxidant genes, transcription factor NF-E2-related-factor-2 (Nrf2), is repressed by epigenetic inactivation of its promoter. Consequently, in contrast to astrocytes or young neurons, maturing neurons possess negligible Nrf2-dependent antioxidant defences, and exhibit no transcriptional responses to Nrf2 activators, or to ablation of Nrf2’s inhibitor Keap1. Neuronal Nrf2 inactivation seems to be required for proper development: in maturing neurons, ectopic Nrf2 expression inhibits neurite outgrowth and aborization, and electrophysiological maturation, including synaptogenesis. These defects arise because Nrf2 activity buffers neuronal redox status, inhibiting maturation processes dependent on redox-sensitive JNK and Wnt pathways. Thus, developmental epigenetic Nrf2 repression weakens neuronal antioxidant defences but is necessary to create an environment that supports neuronal development.
ArticleNumber 7066
Author McKay, Sean
Chowdhry, Sudhir
Al-Mubarak, Bashayer
Meakin, Paul J.
Serio, Andrea
Scannevin, Robert H.
Hardingham, Giles E.
Deighton, Ruth F.
Wheelan, Nicola
Hasel, Philip
Bilican, Bilada
Baxter, Paul
Márkus, Nóra M.
Wyllie, David J.A.
Chandran, Siddharthan
Hayes, John D.
Bell, Karen F.S.
Martel, Marc-André
Ashford, Michael L.J.
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  organization: Centre for Integrative Physiology, University of Edinburgh
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/25967870$$D View this record in MEDLINE/PubMed
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ContentType Journal Article
Copyright The Author(s) 2015
Copyright Nature Publishing Group May 2015
Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. 2015 Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved.
Copyright_xml – notice: The Author(s) 2015
– notice: Copyright Nature Publishing Group May 2015
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  doi: 10.1073/pnas.1402097111
– volume: 341
  start-page: 274
  year: 2012
  ident: BFncomms8066_CR59
  publication-title: J. Pharmacol. Exp. Ther.
  doi: 10.1124/jpet.111.190132
SSID ssj0000391844
Score 2.5261326
Snippet Forebrain neurons have weak intrinsic antioxidant defences compared with astrocytes, but the molecular basis and purpose of this is poorly understood. We show...
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SubjectTerms 13/100
13/106
13/109
13/51
13/95
14/35
14/63
38/15
631/136/368
631/378/2584
631/378/2596/1308
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Adaptor Proteins, Signal Transducing - genetics
Adaptor Proteins, Signal Transducing - metabolism
Animals
Antioxidants
Antioxidants - metabolism
Cerebral Cortex - cytology
Cerebral Cortex - embryology
Cytoskeletal Proteins - genetics
Cytoskeletal Proteins - metabolism
Electrophysiological Phenomena
Epigenesis, Genetic - physiology
Epigenetics
Gene expression
Gene Expression Regulation, Developmental - physiology
Humanities and Social Sciences
Inactivation
Kelch-Like ECH-Associated Protein 1
Mice
Mice, Knockout
multidisciplinary
Neurons
Neurons - physiology
NF-E2-Related Factor 2 - genetics
NF-E2-Related Factor 2 - metabolism
Oxidative stress
Science
Science (multidisciplinary)
Transcription factors
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Title Neuronal development is promoted by weakened intrinsic antioxidant defences due to epigenetic repression of Nrf2
URI https://link.springer.com/article/10.1038/ncomms8066
https://www.ncbi.nlm.nih.gov/pubmed/25967870
https://www.proquest.com/docview/1680432598
https://www.proquest.com/docview/1680955398
https://pubmed.ncbi.nlm.nih.gov/PMC4441249
Volume 6
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