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 in | Nature communications Vol. 6; no. 1; p. 7066 |
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Main Authors | , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
13.05.2015
Nature Publishing Group Nature Pub. Group |
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Online Access | Get full text |
ISSN | 2041-1723 2041-1723 |
DOI | 10.1038/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. |
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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. |
Author_xml | – sequence: 1 givenname: Karen F.S. surname: Bell fullname: Bell, Karen F.S. organization: Centre for Integrative Physiology, University of Edinburgh – sequence: 2 givenname: Bashayer surname: Al-Mubarak fullname: Al-Mubarak, Bashayer organization: Centre for Integrative Physiology, University of Edinburgh – sequence: 3 givenname: Marc-André surname: Martel fullname: Martel, Marc-André organization: Centre for Integrative Physiology, University of Edinburgh – sequence: 4 givenname: Sean surname: McKay fullname: McKay, Sean organization: Centre for Integrative Physiology, University of Edinburgh – sequence: 5 givenname: Nicola surname: Wheelan fullname: Wheelan, Nicola organization: Centre for Integrative Physiology, University of Edinburgh – sequence: 6 givenname: Philip surname: Hasel fullname: Hasel, Philip organization: Centre for Integrative Physiology, University of Edinburgh – sequence: 7 givenname: Nóra M. surname: Márkus fullname: Márkus, Nóra M. organization: Centre for Integrative Physiology, University of Edinburgh – sequence: 8 givenname: Paul surname: Baxter fullname: Baxter, Paul organization: Centre for Integrative Physiology, University of Edinburgh – sequence: 9 givenname: Ruth F. surname: Deighton fullname: Deighton, Ruth F. organization: Centre for Integrative Physiology, University of Edinburgh – sequence: 10 givenname: Andrea surname: Serio fullname: Serio, Andrea organization: MRC Centre for Regenerative Medicine, University of Edinburgh – sequence: 11 givenname: Bilada surname: Bilican fullname: Bilican, Bilada organization: MRC Centre for Regenerative Medicine, University of Edinburgh – sequence: 12 givenname: Sudhir surname: Chowdhry fullname: Chowdhry, Sudhir organization: Medical Research Institute, University of Dundee, Ninewells Hospital and Medical School – sequence: 13 givenname: Paul J. surname: Meakin fullname: Meakin, Paul J. organization: Medical Research Institute, University of Dundee, Ninewells Hospital and Medical School – sequence: 14 givenname: Michael L.J. surname: Ashford fullname: Ashford, Michael L.J. organization: Medical Research Institute, University of Dundee, Ninewells Hospital and Medical School – sequence: 15 givenname: David J.A. surname: Wyllie fullname: Wyllie, David J.A. organization: Centre for Integrative Physiology, University of Edinburgh – sequence: 16 givenname: Robert H. surname: Scannevin fullname: Scannevin, Robert H. organization: Biogen Idec, 14 Cambridge Center – sequence: 17 givenname: Siddharthan surname: Chandran fullname: Chandran, Siddharthan organization: MRC Centre for Regenerative Medicine, University of Edinburgh – sequence: 18 givenname: John D. surname: Hayes fullname: Hayes, John D. organization: Medical Research Institute, University of Dundee, Ninewells Hospital and Medical School – sequence: 19 givenname: Giles E. surname: Hardingham fullname: Hardingham, Giles E. email: Giles.Hardingham@ed.ac.uk organization: Centre for Integrative Physiology, University of Edinburgh |
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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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Title | Neuronal development is promoted by weakened intrinsic antioxidant defences due to epigenetic repression of Nrf2 |
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