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Enriched conditioning expands the regenerative ability of sensory neurons after spinal cord injury via neuronal intrinsic redox signaling

Overcoming the restricted axonal regenerative ability that limits functional repair following a central nervous system injury remains a challenge. Here we report a regenerative paradigm that we call enriched conditioning, which combines environmental enrichment (EE) followed by a conditioning sciati...

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Autores principales: De Virgiliis, Francesco, Hutson, Thomas H., Palmisano, Ilaria, Amachree, Sarah, Miao, Jian, Zhou, Luming, Todorova, Rositsa, Thompson, Richard, Danzi, Matt C., Lemmon, Vance P., Bixby, John L., Wittig, Ilka, Shah, Ajay M., Di Giovanni, Simone
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7752916/
https://www.ncbi.nlm.nih.gov/pubmed/33349630
http://dx.doi.org/10.1038/s41467-020-20179-z
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author De Virgiliis, Francesco
Hutson, Thomas H.
Palmisano, Ilaria
Amachree, Sarah
Miao, Jian
Zhou, Luming
Todorova, Rositsa
Thompson, Richard
Danzi, Matt C.
Lemmon, Vance P.
Bixby, John L.
Wittig, Ilka
Shah, Ajay M.
Di Giovanni, Simone
author_facet De Virgiliis, Francesco
Hutson, Thomas H.
Palmisano, Ilaria
Amachree, Sarah
Miao, Jian
Zhou, Luming
Todorova, Rositsa
Thompson, Richard
Danzi, Matt C.
Lemmon, Vance P.
Bixby, John L.
Wittig, Ilka
Shah, Ajay M.
Di Giovanni, Simone
author_sort De Virgiliis, Francesco
collection PubMed
description Overcoming the restricted axonal regenerative ability that limits functional repair following a central nervous system injury remains a challenge. Here we report a regenerative paradigm that we call enriched conditioning, which combines environmental enrichment (EE) followed by a conditioning sciatic nerve axotomy that precedes a spinal cord injury (SCI). Enriched conditioning significantly increases the regenerative ability of dorsal root ganglia (DRG) sensory neurons compared to EE or a conditioning injury alone, propelling axon growth well beyond the spinal injury site. Mechanistically, we established that enriched conditioning relies on the unique neuronal intrinsic signaling axis PKC-STAT3-NADPH oxidase 2 (NOX2), enhancing redox signaling as shown by redox proteomics in DRG. Finally, NOX2 conditional deletion or overexpression respectively blocked or phenocopied enriched conditioning-dependent axon regeneration after SCI leading to improved functional recovery. These studies provide a paradigm that drives the regenerative ability of sensory neurons offering a potential redox-dependent regenerative model for mechanistic and therapeutic discoveries.
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spelling pubmed-77529162021-01-11 Enriched conditioning expands the regenerative ability of sensory neurons after spinal cord injury via neuronal intrinsic redox signaling De Virgiliis, Francesco Hutson, Thomas H. Palmisano, Ilaria Amachree, Sarah Miao, Jian Zhou, Luming Todorova, Rositsa Thompson, Richard Danzi, Matt C. Lemmon, Vance P. Bixby, John L. Wittig, Ilka Shah, Ajay M. Di Giovanni, Simone Nat Commun Article Overcoming the restricted axonal regenerative ability that limits functional repair following a central nervous system injury remains a challenge. Here we report a regenerative paradigm that we call enriched conditioning, which combines environmental enrichment (EE) followed by a conditioning sciatic nerve axotomy that precedes a spinal cord injury (SCI). Enriched conditioning significantly increases the regenerative ability of dorsal root ganglia (DRG) sensory neurons compared to EE or a conditioning injury alone, propelling axon growth well beyond the spinal injury site. Mechanistically, we established that enriched conditioning relies on the unique neuronal intrinsic signaling axis PKC-STAT3-NADPH oxidase 2 (NOX2), enhancing redox signaling as shown by redox proteomics in DRG. Finally, NOX2 conditional deletion or overexpression respectively blocked or phenocopied enriched conditioning-dependent axon regeneration after SCI leading to improved functional recovery. These studies provide a paradigm that drives the regenerative ability of sensory neurons offering a potential redox-dependent regenerative model for mechanistic and therapeutic discoveries. Nature Publishing Group UK 2020-12-21 /pmc/articles/PMC7752916/ /pubmed/33349630 http://dx.doi.org/10.1038/s41467-020-20179-z Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
De Virgiliis, Francesco
Hutson, Thomas H.
Palmisano, Ilaria
Amachree, Sarah
Miao, Jian
Zhou, Luming
Todorova, Rositsa
Thompson, Richard
Danzi, Matt C.
Lemmon, Vance P.
Bixby, John L.
Wittig, Ilka
Shah, Ajay M.
Di Giovanni, Simone
Enriched conditioning expands the regenerative ability of sensory neurons after spinal cord injury via neuronal intrinsic redox signaling
title Enriched conditioning expands the regenerative ability of sensory neurons after spinal cord injury via neuronal intrinsic redox signaling
title_full Enriched conditioning expands the regenerative ability of sensory neurons after spinal cord injury via neuronal intrinsic redox signaling
title_fullStr Enriched conditioning expands the regenerative ability of sensory neurons after spinal cord injury via neuronal intrinsic redox signaling
title_full_unstemmed Enriched conditioning expands the regenerative ability of sensory neurons after spinal cord injury via neuronal intrinsic redox signaling
title_short Enriched conditioning expands the regenerative ability of sensory neurons after spinal cord injury via neuronal intrinsic redox signaling
title_sort enriched conditioning expands the regenerative ability of sensory neurons after spinal cord injury via neuronal intrinsic redox signaling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7752916/
https://www.ncbi.nlm.nih.gov/pubmed/33349630
http://dx.doi.org/10.1038/s41467-020-20179-z
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