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Reversible silencing of lumbar spinal interneurons unmasks a task-specific network for securing hindlimb alternation
Neural circuitry in the lumbar spinal cord governs two principal features of locomotion, rhythm and pattern, which reflect intra- and interlimb movement. These features are functionally organized into a hierarchy that precisely controls stepping in a stereotypic, speed-dependent fashion. Here, we sh...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5719045/ https://www.ncbi.nlm.nih.gov/pubmed/29213073 http://dx.doi.org/10.1038/s41467-017-02033-x |
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author | Pocratsky, Amanda M. Burke, Darlene A. Morehouse, Johnny R. Beare, Jason E. Riegler, Amberly S. Tsoulfas, Pantelis States, Gregory J. R. Whittemore, Scott R. Magnuson, David S. K. |
author_facet | Pocratsky, Amanda M. Burke, Darlene A. Morehouse, Johnny R. Beare, Jason E. Riegler, Amberly S. Tsoulfas, Pantelis States, Gregory J. R. Whittemore, Scott R. Magnuson, David S. K. |
author_sort | Pocratsky, Amanda M. |
collection | PubMed |
description | Neural circuitry in the lumbar spinal cord governs two principal features of locomotion, rhythm and pattern, which reflect intra- and interlimb movement. These features are functionally organized into a hierarchy that precisely controls stepping in a stereotypic, speed-dependent fashion. Here, we show that a specific component of the locomotor pattern can be independently manipulated. Silencing spinal L2 interneurons that project to L5 selectively disrupts hindlimb alternation allowing a continuum of walking to hopping to emerge from the otherwise intact network. This perturbation, which is independent of speed and occurs spontaneously with each step, does not disrupt multi-joint movements or forelimb alternation, nor does it translate to a non-weight-bearing locomotor activity. Both the underlying rhythm and the usual relationship between speed and spatiotemporal characteristics of stepping persist. These data illustrate that hindlimb alternation can be manipulated independently from other core features of stepping, revealing a striking freedom in an otherwise precisely controlled system. |
format | Online Article Text |
id | pubmed-5719045 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57190452017-12-08 Reversible silencing of lumbar spinal interneurons unmasks a task-specific network for securing hindlimb alternation Pocratsky, Amanda M. Burke, Darlene A. Morehouse, Johnny R. Beare, Jason E. Riegler, Amberly S. Tsoulfas, Pantelis States, Gregory J. R. Whittemore, Scott R. Magnuson, David S. K. Nat Commun Article Neural circuitry in the lumbar spinal cord governs two principal features of locomotion, rhythm and pattern, which reflect intra- and interlimb movement. These features are functionally organized into a hierarchy that precisely controls stepping in a stereotypic, speed-dependent fashion. Here, we show that a specific component of the locomotor pattern can be independently manipulated. Silencing spinal L2 interneurons that project to L5 selectively disrupts hindlimb alternation allowing a continuum of walking to hopping to emerge from the otherwise intact network. This perturbation, which is independent of speed and occurs spontaneously with each step, does not disrupt multi-joint movements or forelimb alternation, nor does it translate to a non-weight-bearing locomotor activity. Both the underlying rhythm and the usual relationship between speed and spatiotemporal characteristics of stepping persist. These data illustrate that hindlimb alternation can be manipulated independently from other core features of stepping, revealing a striking freedom in an otherwise precisely controlled system. Nature Publishing Group UK 2017-12-06 /pmc/articles/PMC5719045/ /pubmed/29213073 http://dx.doi.org/10.1038/s41467-017-02033-x Text en © The Author(s) 2017 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 Pocratsky, Amanda M. Burke, Darlene A. Morehouse, Johnny R. Beare, Jason E. Riegler, Amberly S. Tsoulfas, Pantelis States, Gregory J. R. Whittemore, Scott R. Magnuson, David S. K. Reversible silencing of lumbar spinal interneurons unmasks a task-specific network for securing hindlimb alternation |
title | Reversible silencing of lumbar spinal interneurons unmasks a task-specific network for securing hindlimb alternation |
title_full | Reversible silencing of lumbar spinal interneurons unmasks a task-specific network for securing hindlimb alternation |
title_fullStr | Reversible silencing of lumbar spinal interneurons unmasks a task-specific network for securing hindlimb alternation |
title_full_unstemmed | Reversible silencing of lumbar spinal interneurons unmasks a task-specific network for securing hindlimb alternation |
title_short | Reversible silencing of lumbar spinal interneurons unmasks a task-specific network for securing hindlimb alternation |
title_sort | reversible silencing of lumbar spinal interneurons unmasks a task-specific network for securing hindlimb alternation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5719045/ https://www.ncbi.nlm.nih.gov/pubmed/29213073 http://dx.doi.org/10.1038/s41467-017-02033-x |
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