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Long ascending propriospinal neurons provide flexible, context-specific control of interlimb coordination

Within the cervical and lumbar spinal enlargements, central pattern generator (CPG) circuitry produces the rhythmic output necessary for limb coordination during locomotion. Long propriospinal neurons that inter-connect these CPGs are thought to secure hindlimb-forelimb coordination, ensuring that d...

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Autores principales: Pocratsky, Amanda M, Shepard, Courtney T, Morehouse, Johnny R, Burke, Darlene A, Riegler, Amberley S, Hardin, Josiah T, Beare, Jason E, Hainline, Casey, States, Gregory JR, Brown, Brandon L, Whittemore, Scott R, Magnuson, David SK
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7527236/
https://www.ncbi.nlm.nih.gov/pubmed/32902379
http://dx.doi.org/10.7554/eLife.53565
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author Pocratsky, Amanda M
Shepard, Courtney T
Morehouse, Johnny R
Burke, Darlene A
Riegler, Amberley S
Hardin, Josiah T
Beare, Jason E
Hainline, Casey
States, Gregory JR
Brown, Brandon L
Whittemore, Scott R
Magnuson, David SK
author_facet Pocratsky, Amanda M
Shepard, Courtney T
Morehouse, Johnny R
Burke, Darlene A
Riegler, Amberley S
Hardin, Josiah T
Beare, Jason E
Hainline, Casey
States, Gregory JR
Brown, Brandon L
Whittemore, Scott R
Magnuson, David SK
author_sort Pocratsky, Amanda M
collection PubMed
description Within the cervical and lumbar spinal enlargements, central pattern generator (CPG) circuitry produces the rhythmic output necessary for limb coordination during locomotion. Long propriospinal neurons that inter-connect these CPGs are thought to secure hindlimb-forelimb coordination, ensuring that diagonal limb pairs move synchronously while the ipsilateral limb pairs move out-of-phase during stepping. Here, we show that silencing long ascending propriospinal neurons (LAPNs) that inter-connect the lumbar and cervical CPGs disrupts left-right limb coupling of each limb pair in the adult rat during overground locomotion on a high-friction surface. These perturbations occurred independent of the locomotor rhythm, intralimb coordination, and speed-dependent (or any other) principal features of locomotion. Strikingly, the functional consequences of silencing LAPNs are highly context-dependent; the phenotype was not expressed during swimming, treadmill stepping, exploratory locomotion, or walking on an uncoated, slick surface. These data reveal surprising flexibility and context-dependence in the control of interlimb coordination during locomotion.
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spelling pubmed-75272362020-10-01 Long ascending propriospinal neurons provide flexible, context-specific control of interlimb coordination Pocratsky, Amanda M Shepard, Courtney T Morehouse, Johnny R Burke, Darlene A Riegler, Amberley S Hardin, Josiah T Beare, Jason E Hainline, Casey States, Gregory JR Brown, Brandon L Whittemore, Scott R Magnuson, David SK eLife Neuroscience Within the cervical and lumbar spinal enlargements, central pattern generator (CPG) circuitry produces the rhythmic output necessary for limb coordination during locomotion. Long propriospinal neurons that inter-connect these CPGs are thought to secure hindlimb-forelimb coordination, ensuring that diagonal limb pairs move synchronously while the ipsilateral limb pairs move out-of-phase during stepping. Here, we show that silencing long ascending propriospinal neurons (LAPNs) that inter-connect the lumbar and cervical CPGs disrupts left-right limb coupling of each limb pair in the adult rat during overground locomotion on a high-friction surface. These perturbations occurred independent of the locomotor rhythm, intralimb coordination, and speed-dependent (or any other) principal features of locomotion. Strikingly, the functional consequences of silencing LAPNs are highly context-dependent; the phenotype was not expressed during swimming, treadmill stepping, exploratory locomotion, or walking on an uncoated, slick surface. These data reveal surprising flexibility and context-dependence in the control of interlimb coordination during locomotion. eLife Sciences Publications, Ltd 2020-09-09 /pmc/articles/PMC7527236/ /pubmed/32902379 http://dx.doi.org/10.7554/eLife.53565 Text en © 2020, Pocratsky et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Pocratsky, Amanda M
Shepard, Courtney T
Morehouse, Johnny R
Burke, Darlene A
Riegler, Amberley S
Hardin, Josiah T
Beare, Jason E
Hainline, Casey
States, Gregory JR
Brown, Brandon L
Whittemore, Scott R
Magnuson, David SK
Long ascending propriospinal neurons provide flexible, context-specific control of interlimb coordination
title Long ascending propriospinal neurons provide flexible, context-specific control of interlimb coordination
title_full Long ascending propriospinal neurons provide flexible, context-specific control of interlimb coordination
title_fullStr Long ascending propriospinal neurons provide flexible, context-specific control of interlimb coordination
title_full_unstemmed Long ascending propriospinal neurons provide flexible, context-specific control of interlimb coordination
title_short Long ascending propriospinal neurons provide flexible, context-specific control of interlimb coordination
title_sort long ascending propriospinal neurons provide flexible, context-specific control of interlimb coordination
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7527236/
https://www.ncbi.nlm.nih.gov/pubmed/32902379
http://dx.doi.org/10.7554/eLife.53565
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