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V2a interneuron diversity tailors spinal circuit organization to control the vigor of locomotor movements

Locomotion is a complex motor task generated by spinal circuits driving motoneurons in a precise sequence to control the timing and vigor of movements, but the underlying circuit logic remains to be understood. Here we reveal, in adult zebrafish, how the diversity and selective distribution of two V...

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Autores principales: Song, Jianren, Dahlberg, Elin, El Manira, Abdeljabbar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6105610/
https://www.ncbi.nlm.nih.gov/pubmed/30135498
http://dx.doi.org/10.1038/s41467-018-05827-9
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author Song, Jianren
Dahlberg, Elin
El Manira, Abdeljabbar
author_facet Song, Jianren
Dahlberg, Elin
El Manira, Abdeljabbar
author_sort Song, Jianren
collection PubMed
description Locomotion is a complex motor task generated by spinal circuits driving motoneurons in a precise sequence to control the timing and vigor of movements, but the underlying circuit logic remains to be understood. Here we reveal, in adult zebrafish, how the diversity and selective distribution of two V2a interneuron types within the locomotor network transform commands into an appropriate, task-dependent circuit organization. Bursting-type V2a interneurons with unidirectional axons predominantly target distal dendrites of slow motoneurons to provide potent, non-linear excitation involving NMDA-dependent potentiation. A second type, non-bursting V2a interneurons with bidirectional axons, predominantly target somata of fast motoneurons, providing weaker, non-potentiating excitation. Together, this ensures the rapid, first-order recruitment of the slow circuit, while reserving the fast circuit for highly salient stimuli involving synchronous inputs. Our results thus identify how interneuron diversity is captured and transformed into a parsimonious task-specific circuit design controlling the vigor of locomotion.
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spelling pubmed-61056102018-08-27 V2a interneuron diversity tailors spinal circuit organization to control the vigor of locomotor movements Song, Jianren Dahlberg, Elin El Manira, Abdeljabbar Nat Commun Article Locomotion is a complex motor task generated by spinal circuits driving motoneurons in a precise sequence to control the timing and vigor of movements, but the underlying circuit logic remains to be understood. Here we reveal, in adult zebrafish, how the diversity and selective distribution of two V2a interneuron types within the locomotor network transform commands into an appropriate, task-dependent circuit organization. Bursting-type V2a interneurons with unidirectional axons predominantly target distal dendrites of slow motoneurons to provide potent, non-linear excitation involving NMDA-dependent potentiation. A second type, non-bursting V2a interneurons with bidirectional axons, predominantly target somata of fast motoneurons, providing weaker, non-potentiating excitation. Together, this ensures the rapid, first-order recruitment of the slow circuit, while reserving the fast circuit for highly salient stimuli involving synchronous inputs. Our results thus identify how interneuron diversity is captured and transformed into a parsimonious task-specific circuit design controlling the vigor of locomotion. Nature Publishing Group UK 2018-08-22 /pmc/articles/PMC6105610/ /pubmed/30135498 http://dx.doi.org/10.1038/s41467-018-05827-9 Text en © The Author(s) 2018 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
Song, Jianren
Dahlberg, Elin
El Manira, Abdeljabbar
V2a interneuron diversity tailors spinal circuit organization to control the vigor of locomotor movements
title V2a interneuron diversity tailors spinal circuit organization to control the vigor of locomotor movements
title_full V2a interneuron diversity tailors spinal circuit organization to control the vigor of locomotor movements
title_fullStr V2a interneuron diversity tailors spinal circuit organization to control the vigor of locomotor movements
title_full_unstemmed V2a interneuron diversity tailors spinal circuit organization to control the vigor of locomotor movements
title_short V2a interneuron diversity tailors spinal circuit organization to control the vigor of locomotor movements
title_sort v2a interneuron diversity tailors spinal circuit organization to control the vigor of locomotor movements
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6105610/
https://www.ncbi.nlm.nih.gov/pubmed/30135498
http://dx.doi.org/10.1038/s41467-018-05827-9
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