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Motor Rhythm Dissection From the Backward Circuit in C. elegans

Motor rhythm is initiated and sustained by oscillatory neuronal activity. We recently discovered that the A-class excitatory motor neurons (MNs) (A-MNs) function as intrinsic oscillators. They drive backward locomotion by generating rhythmic postsynaptic currents (rPSCs) in body wall muscles. Molecu...

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Detalles Bibliográficos
Autores principales: Yu, Bin, Wang, Ya, Gao, Shangbang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8966088/
https://www.ncbi.nlm.nih.gov/pubmed/35370545
http://dx.doi.org/10.3389/fnmol.2022.845733
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author Yu, Bin
Wang, Ya
Gao, Shangbang
author_facet Yu, Bin
Wang, Ya
Gao, Shangbang
author_sort Yu, Bin
collection PubMed
description Motor rhythm is initiated and sustained by oscillatory neuronal activity. We recently discovered that the A-class excitatory motor neurons (MNs) (A-MNs) function as intrinsic oscillators. They drive backward locomotion by generating rhythmic postsynaptic currents (rPSCs) in body wall muscles. Molecular underpinning of the rPSCs, however, is not fully elucidated. We report here that there are three types of the rPSC patterns, namely the phasic, tonic, and long-lasting, each with distinct kinetics and channel-dependence. The Na(+) leak channel is required for all rPSC patterns. The tonic rPSCs exhibit strong dependence on the high-voltage-gated Ca(2+) channels. Three K(+) channels, the BK-type Ca(2+)-activated K(+) channel, Na(+)-activated K(+) channel, and voltage-gated K(+) channel (Kv4), primarily inhibit tonic and long-lasting rPSCs with varying degrees and preferences. The elaborate regulation of rPSCs by different channels, through increasing or decreasing the rPSCs frequency and/or charge, correlates with the changes in the reversal velocity for respective channel mutants. The molecular dissection of different A-MNs-rPSC components therefore reveals different mechanisms for multiplex motor rhythm.
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spelling pubmed-89660882022-03-31 Motor Rhythm Dissection From the Backward Circuit in C. elegans Yu, Bin Wang, Ya Gao, Shangbang Front Mol Neurosci Molecular Neuroscience Motor rhythm is initiated and sustained by oscillatory neuronal activity. We recently discovered that the A-class excitatory motor neurons (MNs) (A-MNs) function as intrinsic oscillators. They drive backward locomotion by generating rhythmic postsynaptic currents (rPSCs) in body wall muscles. Molecular underpinning of the rPSCs, however, is not fully elucidated. We report here that there are three types of the rPSC patterns, namely the phasic, tonic, and long-lasting, each with distinct kinetics and channel-dependence. The Na(+) leak channel is required for all rPSC patterns. The tonic rPSCs exhibit strong dependence on the high-voltage-gated Ca(2+) channels. Three K(+) channels, the BK-type Ca(2+)-activated K(+) channel, Na(+)-activated K(+) channel, and voltage-gated K(+) channel (Kv4), primarily inhibit tonic and long-lasting rPSCs with varying degrees and preferences. The elaborate regulation of rPSCs by different channels, through increasing or decreasing the rPSCs frequency and/or charge, correlates with the changes in the reversal velocity for respective channel mutants. The molecular dissection of different A-MNs-rPSC components therefore reveals different mechanisms for multiplex motor rhythm. Frontiers Media S.A. 2022-03-16 /pmc/articles/PMC8966088/ /pubmed/35370545 http://dx.doi.org/10.3389/fnmol.2022.845733 Text en Copyright © 2022 Yu, Wang and Gao. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Molecular Neuroscience
Yu, Bin
Wang, Ya
Gao, Shangbang
Motor Rhythm Dissection From the Backward Circuit in C. elegans
title Motor Rhythm Dissection From the Backward Circuit in C. elegans
title_full Motor Rhythm Dissection From the Backward Circuit in C. elegans
title_fullStr Motor Rhythm Dissection From the Backward Circuit in C. elegans
title_full_unstemmed Motor Rhythm Dissection From the Backward Circuit in C. elegans
title_short Motor Rhythm Dissection From the Backward Circuit in C. elegans
title_sort motor rhythm dissection from the backward circuit in c. elegans
topic Molecular Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8966088/
https://www.ncbi.nlm.nih.gov/pubmed/35370545
http://dx.doi.org/10.3389/fnmol.2022.845733
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