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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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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. |
format | Online Article Text |
id | pubmed-6701946 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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