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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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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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. |
format | Online Article Text |
id | pubmed-7752916 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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