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Neural Control of Startle-Induced Locomotion by the Mushroom Bodies and Associated Neurons in Drosophila

Startle-induced locomotion is commonly used in Drosophila research to monitor locomotor reactivity and its progressive decline with age or under various neuropathological conditions. A widely used paradigm is startle-induced negative geotaxis (SING), in which flies entrapped in a narrow column react...

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Autores principales: Sun, Jun, Xu, An Qi, Giraud, Julia, Poppinga, Haiko, Riemensperger, Thomas, Fiala, André, Birman, Serge
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5882849/
https://www.ncbi.nlm.nih.gov/pubmed/29643770
http://dx.doi.org/10.3389/fnsys.2018.00006
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author Sun, Jun
Xu, An Qi
Giraud, Julia
Poppinga, Haiko
Riemensperger, Thomas
Fiala, André
Birman, Serge
author_facet Sun, Jun
Xu, An Qi
Giraud, Julia
Poppinga, Haiko
Riemensperger, Thomas
Fiala, André
Birman, Serge
author_sort Sun, Jun
collection PubMed
description Startle-induced locomotion is commonly used in Drosophila research to monitor locomotor reactivity and its progressive decline with age or under various neuropathological conditions. A widely used paradigm is startle-induced negative geotaxis (SING), in which flies entrapped in a narrow column react to a gentle mechanical shock by climbing rapidly upwards. Here we combined in vivo manipulation of neuronal activity and splitGFP reconstitution across cells to search for brain neurons and putative circuits that regulate this behavior. We show that the activity of specific clusters of dopaminergic neurons (DANs) afferent to the mushroom bodies (MBs) modulates SING, and that DAN-mediated SING regulation requires expression of the DA receptor Dop1R1/Dumb, but not Dop1R2/Damb, in intrinsic MB Kenyon cells (KCs). We confirmed our previous observation that activating the MB α'β', but not αβ, KCs decreased the SING response, and we identified further MB neurons implicated in SING control, including KCs of the γ lobe and two subtypes of MB output neurons (MBONs). We also observed that co-activating the αβ KCs antagonizes α'β' and γ KC-mediated SING modulation, suggesting the existence of subtle regulation mechanisms between the different MB lobes in locomotion control. Overall, this study contributes to an emerging picture of the brain circuits modulating locomotor reactivity in Drosophila that appear both to overlap and differ from those underlying associative learning and memory, sleep/wake state and stress-induced hyperactivity.
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spelling pubmed-58828492018-04-11 Neural Control of Startle-Induced Locomotion by the Mushroom Bodies and Associated Neurons in Drosophila Sun, Jun Xu, An Qi Giraud, Julia Poppinga, Haiko Riemensperger, Thomas Fiala, André Birman, Serge Front Syst Neurosci Neuroscience Startle-induced locomotion is commonly used in Drosophila research to monitor locomotor reactivity and its progressive decline with age or under various neuropathological conditions. A widely used paradigm is startle-induced negative geotaxis (SING), in which flies entrapped in a narrow column react to a gentle mechanical shock by climbing rapidly upwards. Here we combined in vivo manipulation of neuronal activity and splitGFP reconstitution across cells to search for brain neurons and putative circuits that regulate this behavior. We show that the activity of specific clusters of dopaminergic neurons (DANs) afferent to the mushroom bodies (MBs) modulates SING, and that DAN-mediated SING regulation requires expression of the DA receptor Dop1R1/Dumb, but not Dop1R2/Damb, in intrinsic MB Kenyon cells (KCs). We confirmed our previous observation that activating the MB α'β', but not αβ, KCs decreased the SING response, and we identified further MB neurons implicated in SING control, including KCs of the γ lobe and two subtypes of MB output neurons (MBONs). We also observed that co-activating the αβ KCs antagonizes α'β' and γ KC-mediated SING modulation, suggesting the existence of subtle regulation mechanisms between the different MB lobes in locomotion control. Overall, this study contributes to an emerging picture of the brain circuits modulating locomotor reactivity in Drosophila that appear both to overlap and differ from those underlying associative learning and memory, sleep/wake state and stress-induced hyperactivity. Frontiers Media S.A. 2018-03-28 /pmc/articles/PMC5882849/ /pubmed/29643770 http://dx.doi.org/10.3389/fnsys.2018.00006 Text en Copyright © 2018 Sun, Xu, Giraud, Poppinga, Riemensperger, Fiala and Birman. http://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 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 Neuroscience
Sun, Jun
Xu, An Qi
Giraud, Julia
Poppinga, Haiko
Riemensperger, Thomas
Fiala, André
Birman, Serge
Neural Control of Startle-Induced Locomotion by the Mushroom Bodies and Associated Neurons in Drosophila
title Neural Control of Startle-Induced Locomotion by the Mushroom Bodies and Associated Neurons in Drosophila
title_full Neural Control of Startle-Induced Locomotion by the Mushroom Bodies and Associated Neurons in Drosophila
title_fullStr Neural Control of Startle-Induced Locomotion by the Mushroom Bodies and Associated Neurons in Drosophila
title_full_unstemmed Neural Control of Startle-Induced Locomotion by the Mushroom Bodies and Associated Neurons in Drosophila
title_short Neural Control of Startle-Induced Locomotion by the Mushroom Bodies and Associated Neurons in Drosophila
title_sort neural control of startle-induced locomotion by the mushroom bodies and associated neurons in drosophila
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5882849/
https://www.ncbi.nlm.nih.gov/pubmed/29643770
http://dx.doi.org/10.3389/fnsys.2018.00006
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