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Formation of somatosensory detour circuits mediates functional recovery following dorsal column injury

Anatomically incomplete spinal cord injuries can be followed by functional recovery mediated, in part, by the formation of intraspinal detour circuits. Here, we show that adult mice recover tactile and proprioceptive function following a unilateral dorsal column lesion. We therefore investigated the...

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Autores principales: Granier, Charlène, Schwarting, Julian, Fourli, Evangelia, Laage-Gaupp, Fabian, Hennrich, Alexandru A., Schmalz, Anja, Jacobi, Anne, Wesolowski, Marta, Conzelmann, Karl Klaus, Bareyre, Florence M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7331809/
https://www.ncbi.nlm.nih.gov/pubmed/32616790
http://dx.doi.org/10.1038/s41598-020-67866-x
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author Granier, Charlène
Schwarting, Julian
Fourli, Evangelia
Laage-Gaupp, Fabian
Hennrich, Alexandru A.
Schmalz, Anja
Jacobi, Anne
Wesolowski, Marta
Conzelmann, Karl Klaus
Bareyre, Florence M.
author_facet Granier, Charlène
Schwarting, Julian
Fourli, Evangelia
Laage-Gaupp, Fabian
Hennrich, Alexandru A.
Schmalz, Anja
Jacobi, Anne
Wesolowski, Marta
Conzelmann, Karl Klaus
Bareyre, Florence M.
author_sort Granier, Charlène
collection PubMed
description Anatomically incomplete spinal cord injuries can be followed by functional recovery mediated, in part, by the formation of intraspinal detour circuits. Here, we show that adult mice recover tactile and proprioceptive function following a unilateral dorsal column lesion. We therefore investigated the basis of this recovery and focused on the plasticity of the dorsal column-medial lemniscus pathway. We show that ascending dorsal root ganglion (DRG) axons branch in the spinal grey matter and substantially increase the number of these collaterals following injury. These sensory fibers exhibit synapsin-positive varicosities, indicating their integration into spinal networks. Using a monosynaptic circuit tracing with rabies viruses injected into the cuneate nucleus, we show the presence of spinal cord neurons that provide a detour pathway to the original target area of DRG axons. Notably the number of contacts between DRG collaterals and those spinal neurons increases by more than 300% after injury. We then characterized these interneurons and showed that the lesion triggers a remodeling of the connectivity pattern. Finally, using re-lesion experiments after initial remodeling of connections, we show that these detour circuits are responsible for the recovery of tactile and proprioceptive function. Taken together our study reveals that detour circuits represent a common blueprint for axonal rewiring after injury.
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spelling pubmed-73318092020-07-06 Formation of somatosensory detour circuits mediates functional recovery following dorsal column injury Granier, Charlène Schwarting, Julian Fourli, Evangelia Laage-Gaupp, Fabian Hennrich, Alexandru A. Schmalz, Anja Jacobi, Anne Wesolowski, Marta Conzelmann, Karl Klaus Bareyre, Florence M. Sci Rep Article Anatomically incomplete spinal cord injuries can be followed by functional recovery mediated, in part, by the formation of intraspinal detour circuits. Here, we show that adult mice recover tactile and proprioceptive function following a unilateral dorsal column lesion. We therefore investigated the basis of this recovery and focused on the plasticity of the dorsal column-medial lemniscus pathway. We show that ascending dorsal root ganglion (DRG) axons branch in the spinal grey matter and substantially increase the number of these collaterals following injury. These sensory fibers exhibit synapsin-positive varicosities, indicating their integration into spinal networks. Using a monosynaptic circuit tracing with rabies viruses injected into the cuneate nucleus, we show the presence of spinal cord neurons that provide a detour pathway to the original target area of DRG axons. Notably the number of contacts between DRG collaterals and those spinal neurons increases by more than 300% after injury. We then characterized these interneurons and showed that the lesion triggers a remodeling of the connectivity pattern. Finally, using re-lesion experiments after initial remodeling of connections, we show that these detour circuits are responsible for the recovery of tactile and proprioceptive function. Taken together our study reveals that detour circuits represent a common blueprint for axonal rewiring after injury. Nature Publishing Group UK 2020-07-02 /pmc/articles/PMC7331809/ /pubmed/32616790 http://dx.doi.org/10.1038/s41598-020-67866-x 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
Granier, Charlène
Schwarting, Julian
Fourli, Evangelia
Laage-Gaupp, Fabian
Hennrich, Alexandru A.
Schmalz, Anja
Jacobi, Anne
Wesolowski, Marta
Conzelmann, Karl Klaus
Bareyre, Florence M.
Formation of somatosensory detour circuits mediates functional recovery following dorsal column injury
title Formation of somatosensory detour circuits mediates functional recovery following dorsal column injury
title_full Formation of somatosensory detour circuits mediates functional recovery following dorsal column injury
title_fullStr Formation of somatosensory detour circuits mediates functional recovery following dorsal column injury
title_full_unstemmed Formation of somatosensory detour circuits mediates functional recovery following dorsal column injury
title_short Formation of somatosensory detour circuits mediates functional recovery following dorsal column injury
title_sort formation of somatosensory detour circuits mediates functional recovery following dorsal column injury
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7331809/
https://www.ncbi.nlm.nih.gov/pubmed/32616790
http://dx.doi.org/10.1038/s41598-020-67866-x
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