Cargando…
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...
Autores principales: | , , , , , , , , , , , |
---|---|
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 |
_version_ | 1783589014811443200 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7527236 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT pocratskyamandam longascendingpropriospinalneuronsprovideflexiblecontextspecificcontrolofinterlimbcoordination AT shepardcourtneyt longascendingpropriospinalneuronsprovideflexiblecontextspecificcontrolofinterlimbcoordination AT morehousejohnnyr longascendingpropriospinalneuronsprovideflexiblecontextspecificcontrolofinterlimbcoordination AT burkedarlenea longascendingpropriospinalneuronsprovideflexiblecontextspecificcontrolofinterlimbcoordination AT riegleramberleys longascendingpropriospinalneuronsprovideflexiblecontextspecificcontrolofinterlimbcoordination AT hardinjosiaht longascendingpropriospinalneuronsprovideflexiblecontextspecificcontrolofinterlimbcoordination AT bearejasone longascendingpropriospinalneuronsprovideflexiblecontextspecificcontrolofinterlimbcoordination AT hainlinecasey longascendingpropriospinalneuronsprovideflexiblecontextspecificcontrolofinterlimbcoordination AT statesgregoryjr longascendingpropriospinalneuronsprovideflexiblecontextspecificcontrolofinterlimbcoordination AT brownbrandonl longascendingpropriospinalneuronsprovideflexiblecontextspecificcontrolofinterlimbcoordination AT whittemorescottr longascendingpropriospinalneuronsprovideflexiblecontextspecificcontrolofinterlimbcoordination AT magnusondavidsk longascendingpropriospinalneuronsprovideflexiblecontextspecificcontrolofinterlimbcoordination |