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Spinal V2b neurons reveal a role for ipsilateral inhibition in speed control

The spinal cord contains a diverse array of interneurons that govern motor output. Traditionally, models of spinal circuits have emphasized the role of inhibition in enforcing reciprocal alternation between left and right sides or flexors and extensors. However, recent work has shown that inhibition...

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Autores principales: Callahan, Rebecca A, Roberts, Richard, Sengupta, Mohini, Kimura, Yukiko, Higashijima, Shin-ichi, Bagnall, Martha W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6701946/
https://www.ncbi.nlm.nih.gov/pubmed/31355747
http://dx.doi.org/10.7554/eLife.47837
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author Callahan, Rebecca A
Roberts, Richard
Sengupta, Mohini
Kimura, Yukiko
Higashijima, Shin-ichi
Bagnall, Martha W
author_facet Callahan, Rebecca A
Roberts, Richard
Sengupta, Mohini
Kimura, Yukiko
Higashijima, Shin-ichi
Bagnall, Martha W
author_sort Callahan, Rebecca A
collection PubMed
description The spinal cord contains a diverse array of interneurons that govern motor output. Traditionally, models of spinal circuits have emphasized the role of inhibition in enforcing reciprocal alternation between left and right sides or flexors and extensors. However, recent work has shown that inhibition also increases coincident with excitation during contraction. Here, using larval zebrafish, we investigate the V2b (Gata3+) class of neurons, which contribute to flexor-extensor alternation but are otherwise poorly understood. Using newly generated transgenic lines we define two stable subclasses with distinct neurotransmitter and morphological properties. These V2b subclasses synapse directly onto motor neurons with differential targeting to speed-specific circuits. In vivo, optogenetic manipulation of V2b activity modulates locomotor frequency: suppressing V2b neurons elicits faster locomotion, whereas activating V2b neurons slows locomotion. We conclude that V2b neurons serve as a brake on axial motor circuits. Together, these results indicate a role for ipsilateral inhibition in speed control.
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spelling pubmed-67019462019-08-22 Spinal V2b neurons reveal a role for ipsilateral inhibition in speed control Callahan, Rebecca A Roberts, Richard Sengupta, Mohini Kimura, Yukiko Higashijima, Shin-ichi Bagnall, Martha W eLife Neuroscience The spinal cord contains a diverse array of interneurons that govern motor output. Traditionally, models of spinal circuits have emphasized the role of inhibition in enforcing reciprocal alternation between left and right sides or flexors and extensors. However, recent work has shown that inhibition also increases coincident with excitation during contraction. Here, using larval zebrafish, we investigate the V2b (Gata3+) class of neurons, which contribute to flexor-extensor alternation but are otherwise poorly understood. Using newly generated transgenic lines we define two stable subclasses with distinct neurotransmitter and morphological properties. These V2b subclasses synapse directly onto motor neurons with differential targeting to speed-specific circuits. In vivo, optogenetic manipulation of V2b activity modulates locomotor frequency: suppressing V2b neurons elicits faster locomotion, whereas activating V2b neurons slows locomotion. We conclude that V2b neurons serve as a brake on axial motor circuits. Together, these results indicate a role for ipsilateral inhibition in speed control. eLife Sciences Publications, Ltd 2019-07-29 /pmc/articles/PMC6701946/ /pubmed/31355747 http://dx.doi.org/10.7554/eLife.47837 Text en © 2019, Callahan 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
Callahan, Rebecca A
Roberts, Richard
Sengupta, Mohini
Kimura, Yukiko
Higashijima, Shin-ichi
Bagnall, Martha W
Spinal V2b neurons reveal a role for ipsilateral inhibition in speed control
title Spinal V2b neurons reveal a role for ipsilateral inhibition in speed control
title_full Spinal V2b neurons reveal a role for ipsilateral inhibition in speed control
title_fullStr Spinal V2b neurons reveal a role for ipsilateral inhibition in speed control
title_full_unstemmed Spinal V2b neurons reveal a role for ipsilateral inhibition in speed control
title_short Spinal V2b neurons reveal a role for ipsilateral inhibition in speed control
title_sort spinal v2b neurons reveal a role for ipsilateral inhibition in speed control
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6701946/
https://www.ncbi.nlm.nih.gov/pubmed/31355747
http://dx.doi.org/10.7554/eLife.47837
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