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Brain-wide analysis of the supraspinal connectome reveals anatomical correlates to functional recovery after spinal injury

The supraspinal connectome is essential for normal behavior and homeostasis and consists of numerous sensory, motor, and autonomic projections from brain to spinal cord. Study of supraspinal control and its restoration after damage has focused mostly on a handful of major populations that carry moto...

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Autores principales: Wang, Zimei, Romanski, Adam, Mehra, Vatsal, Wang, Yunfang, Brannigan, Matthew, Campbell, Benjamin C, Petsko, Gregory A, Tsoulfas, Pantelis, Blackmore, Murray G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9345604/
https://www.ncbi.nlm.nih.gov/pubmed/35838234
http://dx.doi.org/10.7554/eLife.76254
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author Wang, Zimei
Romanski, Adam
Mehra, Vatsal
Wang, Yunfang
Brannigan, Matthew
Campbell, Benjamin C
Petsko, Gregory A
Tsoulfas, Pantelis
Blackmore, Murray G
author_facet Wang, Zimei
Romanski, Adam
Mehra, Vatsal
Wang, Yunfang
Brannigan, Matthew
Campbell, Benjamin C
Petsko, Gregory A
Tsoulfas, Pantelis
Blackmore, Murray G
author_sort Wang, Zimei
collection PubMed
description The supraspinal connectome is essential for normal behavior and homeostasis and consists of numerous sensory, motor, and autonomic projections from brain to spinal cord. Study of supraspinal control and its restoration after damage has focused mostly on a handful of major populations that carry motor commands, with only limited consideration of dozens more that provide autonomic or crucial motor modulation. Here, we assemble an experimental workflow to rapidly profile the entire supraspinal mesoconnectome in adult mice and disseminate the output in a web-based resource. Optimized viral labeling, 3D imaging, and registration to a mouse digital neuroanatomical atlas assigned tens of thousands of supraspinal neurons to 69 identified regions. We demonstrate the ability of this approach to clarify essential points of topographic mapping between spinal levels, measure population-specific sensitivity to spinal injury, and test the relationships between region-specific neuronal sparing and variability in functional recovery. This work will spur progress by broadening understanding of essential but understudied supraspinal populations.
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spelling pubmed-93456042022-08-03 Brain-wide analysis of the supraspinal connectome reveals anatomical correlates to functional recovery after spinal injury Wang, Zimei Romanski, Adam Mehra, Vatsal Wang, Yunfang Brannigan, Matthew Campbell, Benjamin C Petsko, Gregory A Tsoulfas, Pantelis Blackmore, Murray G eLife Neuroscience The supraspinal connectome is essential for normal behavior and homeostasis and consists of numerous sensory, motor, and autonomic projections from brain to spinal cord. Study of supraspinal control and its restoration after damage has focused mostly on a handful of major populations that carry motor commands, with only limited consideration of dozens more that provide autonomic or crucial motor modulation. Here, we assemble an experimental workflow to rapidly profile the entire supraspinal mesoconnectome in adult mice and disseminate the output in a web-based resource. Optimized viral labeling, 3D imaging, and registration to a mouse digital neuroanatomical atlas assigned tens of thousands of supraspinal neurons to 69 identified regions. We demonstrate the ability of this approach to clarify essential points of topographic mapping between spinal levels, measure population-specific sensitivity to spinal injury, and test the relationships between region-specific neuronal sparing and variability in functional recovery. This work will spur progress by broadening understanding of essential but understudied supraspinal populations. eLife Sciences Publications, Ltd 2022-07-15 /pmc/articles/PMC9345604/ /pubmed/35838234 http://dx.doi.org/10.7554/eLife.76254 Text en © 2022, Wang et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Wang, Zimei
Romanski, Adam
Mehra, Vatsal
Wang, Yunfang
Brannigan, Matthew
Campbell, Benjamin C
Petsko, Gregory A
Tsoulfas, Pantelis
Blackmore, Murray G
Brain-wide analysis of the supraspinal connectome reveals anatomical correlates to functional recovery after spinal injury
title Brain-wide analysis of the supraspinal connectome reveals anatomical correlates to functional recovery after spinal injury
title_full Brain-wide analysis of the supraspinal connectome reveals anatomical correlates to functional recovery after spinal injury
title_fullStr Brain-wide analysis of the supraspinal connectome reveals anatomical correlates to functional recovery after spinal injury
title_full_unstemmed Brain-wide analysis of the supraspinal connectome reveals anatomical correlates to functional recovery after spinal injury
title_short Brain-wide analysis of the supraspinal connectome reveals anatomical correlates to functional recovery after spinal injury
title_sort brain-wide analysis of the supraspinal connectome reveals anatomical correlates to functional recovery after spinal injury
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9345604/
https://www.ncbi.nlm.nih.gov/pubmed/35838234
http://dx.doi.org/10.7554/eLife.76254
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