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Corticospinal circuit remodeling after central nervous system injury is dependent on neuronal activity
The remodeling of supraspinal axonal circuits mediates functional recovery after spinal cord injury. This process critically depends on the selection of appropriate synaptic connections between cortical projection and spinal relay neurons. To unravel the principles that guide this target selection,...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829605/ https://www.ncbi.nlm.nih.gov/pubmed/31391209 http://dx.doi.org/10.1084/jem.20181406 |
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author | Bradley, Peter M. Denecke, Carmen K. Aljovic, Almir Schmalz, Anja Kerschensteiner, Martin Bareyre, Florence M. |
author_facet | Bradley, Peter M. Denecke, Carmen K. Aljovic, Almir Schmalz, Anja Kerschensteiner, Martin Bareyre, Florence M. |
author_sort | Bradley, Peter M. |
collection | PubMed |
description | The remodeling of supraspinal axonal circuits mediates functional recovery after spinal cord injury. This process critically depends on the selection of appropriate synaptic connections between cortical projection and spinal relay neurons. To unravel the principles that guide this target selection, we used genetic and chemogenetic tools to modulate NMDA receptor (NMDAR) integrity and function, CREB-mediated transcription, and neuronal firing of relay neurons during injury-induced corticospinal remodeling. We show that NMDAR signaling and CREB-mediated transcription maintain nascent corticospinal tract (CST)–relay neuron contacts. These activity-dependent signals act during a defined period of circuit remodeling and do not affect mature or uninjured circuits. Furthermore, chemogenetic modulation of relay neuron activity reveals that the regrowing CST axons select their postsynaptic partners in a competitive manner and that preventing such activity-dependent shaping of corticospinal circuits limits motor recovery after spinal cord injury. |
format | Online Article Text |
id | pubmed-6829605 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-68296052020-05-04 Corticospinal circuit remodeling after central nervous system injury is dependent on neuronal activity Bradley, Peter M. Denecke, Carmen K. Aljovic, Almir Schmalz, Anja Kerschensteiner, Martin Bareyre, Florence M. J Exp Med Research Articles The remodeling of supraspinal axonal circuits mediates functional recovery after spinal cord injury. This process critically depends on the selection of appropriate synaptic connections between cortical projection and spinal relay neurons. To unravel the principles that guide this target selection, we used genetic and chemogenetic tools to modulate NMDA receptor (NMDAR) integrity and function, CREB-mediated transcription, and neuronal firing of relay neurons during injury-induced corticospinal remodeling. We show that NMDAR signaling and CREB-mediated transcription maintain nascent corticospinal tract (CST)–relay neuron contacts. These activity-dependent signals act during a defined period of circuit remodeling and do not affect mature or uninjured circuits. Furthermore, chemogenetic modulation of relay neuron activity reveals that the regrowing CST axons select their postsynaptic partners in a competitive manner and that preventing such activity-dependent shaping of corticospinal circuits limits motor recovery after spinal cord injury. Rockefeller University Press 2019-11-04 2019-08-07 /pmc/articles/PMC6829605/ /pubmed/31391209 http://dx.doi.org/10.1084/jem.20181406 Text en © 2019 Bradley et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Research Articles Bradley, Peter M. Denecke, Carmen K. Aljovic, Almir Schmalz, Anja Kerschensteiner, Martin Bareyre, Florence M. Corticospinal circuit remodeling after central nervous system injury is dependent on neuronal activity |
title | Corticospinal circuit remodeling after central nervous system injury is dependent on neuronal activity |
title_full | Corticospinal circuit remodeling after central nervous system injury is dependent on neuronal activity |
title_fullStr | Corticospinal circuit remodeling after central nervous system injury is dependent on neuronal activity |
title_full_unstemmed | Corticospinal circuit remodeling after central nervous system injury is dependent on neuronal activity |
title_short | Corticospinal circuit remodeling after central nervous system injury is dependent on neuronal activity |
title_sort | corticospinal circuit remodeling after central nervous system injury is dependent on neuronal activity |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829605/ https://www.ncbi.nlm.nih.gov/pubmed/31391209 http://dx.doi.org/10.1084/jem.20181406 |
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