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Organelle calcium-derived voltage oscillations in pacemaker neurons drive the motor program for food-seeking behavior in Aplysia

The expression of motivated behaviors depends on both external and internally arising neural stimuli, yet the intrinsic releasing mechanisms for such variably occurring behaviors remain elusive. In isolated nervous system preparations of Aplysia, we have found that irregularly expressed cycles of mo...

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Autores principales: Bédécarrats, Alexis, Puygrenier, Laura, Castro O'Byrne, John, Lade, Quentin, Simmers, John, Nargeot, Romuald
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8263059/
https://www.ncbi.nlm.nih.gov/pubmed/34190043
http://dx.doi.org/10.7554/eLife.68651
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author Bédécarrats, Alexis
Puygrenier, Laura
Castro O'Byrne, John
Lade, Quentin
Simmers, John
Nargeot, Romuald
author_facet Bédécarrats, Alexis
Puygrenier, Laura
Castro O'Byrne, John
Lade, Quentin
Simmers, John
Nargeot, Romuald
author_sort Bédécarrats, Alexis
collection PubMed
description The expression of motivated behaviors depends on both external and internally arising neural stimuli, yet the intrinsic releasing mechanisms for such variably occurring behaviors remain elusive. In isolated nervous system preparations of Aplysia, we have found that irregularly expressed cycles of motor output underlying food-seeking behavior arise from regular membrane potential oscillations of varying magnitude in an identified pair of interneurons (B63) in the bilateral buccal ganglia. This rhythmic signal, which is specific to the B63 cells, is generated by organelle-derived intracellular calcium fluxes that activate voltage-independent plasma membrane channels. The resulting voltage oscillation spreads throughout a subset of gap junction-coupled buccal network neurons and by triggering plateau potential-mediated bursts in B63, can initiate motor output driving food-seeking action. Thus, an atypical neuronal pacemaker mechanism, based on rhythmic intracellular calcium store release and intercellular propagation, can act as an autonomous intrinsic releaser for the occurrence of a motivated behavior.
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spelling pubmed-82630592021-07-12 Organelle calcium-derived voltage oscillations in pacemaker neurons drive the motor program for food-seeking behavior in Aplysia Bédécarrats, Alexis Puygrenier, Laura Castro O'Byrne, John Lade, Quentin Simmers, John Nargeot, Romuald eLife Neuroscience The expression of motivated behaviors depends on both external and internally arising neural stimuli, yet the intrinsic releasing mechanisms for such variably occurring behaviors remain elusive. In isolated nervous system preparations of Aplysia, we have found that irregularly expressed cycles of motor output underlying food-seeking behavior arise from regular membrane potential oscillations of varying magnitude in an identified pair of interneurons (B63) in the bilateral buccal ganglia. This rhythmic signal, which is specific to the B63 cells, is generated by organelle-derived intracellular calcium fluxes that activate voltage-independent plasma membrane channels. The resulting voltage oscillation spreads throughout a subset of gap junction-coupled buccal network neurons and by triggering plateau potential-mediated bursts in B63, can initiate motor output driving food-seeking action. Thus, an atypical neuronal pacemaker mechanism, based on rhythmic intracellular calcium store release and intercellular propagation, can act as an autonomous intrinsic releaser for the occurrence of a motivated behavior. eLife Sciences Publications, Ltd 2021-06-30 /pmc/articles/PMC8263059/ /pubmed/34190043 http://dx.doi.org/10.7554/eLife.68651 Text en © 2021, Bédécarrats et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Bédécarrats, Alexis
Puygrenier, Laura
Castro O'Byrne, John
Lade, Quentin
Simmers, John
Nargeot, Romuald
Organelle calcium-derived voltage oscillations in pacemaker neurons drive the motor program for food-seeking behavior in Aplysia
title Organelle calcium-derived voltage oscillations in pacemaker neurons drive the motor program for food-seeking behavior in Aplysia
title_full Organelle calcium-derived voltage oscillations in pacemaker neurons drive the motor program for food-seeking behavior in Aplysia
title_fullStr Organelle calcium-derived voltage oscillations in pacemaker neurons drive the motor program for food-seeking behavior in Aplysia
title_full_unstemmed Organelle calcium-derived voltage oscillations in pacemaker neurons drive the motor program for food-seeking behavior in Aplysia
title_short Organelle calcium-derived voltage oscillations in pacemaker neurons drive the motor program for food-seeking behavior in Aplysia
title_sort organelle calcium-derived voltage oscillations in pacemaker neurons drive the motor program for food-seeking behavior in aplysia
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8263059/
https://www.ncbi.nlm.nih.gov/pubmed/34190043
http://dx.doi.org/10.7554/eLife.68651
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