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Mechanosensory circuits coordinate two opposing motor actions in Drosophila feeding

Mechanoreception detects physical forces in the senses of hearing, touch, and proprioception. Here, we show that labellar mechanoreception wires two motor circuits to facilitate and terminate Drosophila feeding. Using patch-clamp recordings, we identified mechanosensory neurons (MSNs) in taste pegs...

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Autores principales: Zhou, Yao, Cao, Li-Hui, Sui, Xiu-Wen, Guo, Xiao-Qing, Luo, Dong-Gen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6531006/
https://www.ncbi.nlm.nih.gov/pubmed/31131327
http://dx.doi.org/10.1126/sciadv.aaw5141
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author Zhou, Yao
Cao, Li-Hui
Sui, Xiu-Wen
Guo, Xiao-Qing
Luo, Dong-Gen
author_facet Zhou, Yao
Cao, Li-Hui
Sui, Xiu-Wen
Guo, Xiao-Qing
Luo, Dong-Gen
author_sort Zhou, Yao
collection PubMed
description Mechanoreception detects physical forces in the senses of hearing, touch, and proprioception. Here, we show that labellar mechanoreception wires two motor circuits to facilitate and terminate Drosophila feeding. Using patch-clamp recordings, we identified mechanosensory neurons (MSNs) in taste pegs of the inner labella and taste bristles of the outer labella, both of which rely on the same mechanoreceptor, NOMPC (no mechanoreceptor potential C), to transduce mechanical deflection. Connecting with distinct brain motor circuits, bristle MSNs drive labellar spread to facilitate feeding and peg MSNs elicit proboscis retraction to terminate feeding. Bitter sense modulates these two mechanosensory circuits in opposing manners, preventing labellar spread by bristle MSNs and promoting proboscis retraction by peg MSNs. Together, these labeled-line circuits enable labellar peg and bristle MSNs to use the same mechanoreceptors to direct opposing feeding actions and differentially integrate gustatory information in shaping feeding decisions.
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spelling pubmed-65310062019-05-26 Mechanosensory circuits coordinate two opposing motor actions in Drosophila feeding Zhou, Yao Cao, Li-Hui Sui, Xiu-Wen Guo, Xiao-Qing Luo, Dong-Gen Sci Adv Research Articles Mechanoreception detects physical forces in the senses of hearing, touch, and proprioception. Here, we show that labellar mechanoreception wires two motor circuits to facilitate and terminate Drosophila feeding. Using patch-clamp recordings, we identified mechanosensory neurons (MSNs) in taste pegs of the inner labella and taste bristles of the outer labella, both of which rely on the same mechanoreceptor, NOMPC (no mechanoreceptor potential C), to transduce mechanical deflection. Connecting with distinct brain motor circuits, bristle MSNs drive labellar spread to facilitate feeding and peg MSNs elicit proboscis retraction to terminate feeding. Bitter sense modulates these two mechanosensory circuits in opposing manners, preventing labellar spread by bristle MSNs and promoting proboscis retraction by peg MSNs. Together, these labeled-line circuits enable labellar peg and bristle MSNs to use the same mechanoreceptors to direct opposing feeding actions and differentially integrate gustatory information in shaping feeding decisions. American Association for the Advancement of Science 2019-05-22 /pmc/articles/PMC6531006/ /pubmed/31131327 http://dx.doi.org/10.1126/sciadv.aaw5141 Text en Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Zhou, Yao
Cao, Li-Hui
Sui, Xiu-Wen
Guo, Xiao-Qing
Luo, Dong-Gen
Mechanosensory circuits coordinate two opposing motor actions in Drosophila feeding
title Mechanosensory circuits coordinate two opposing motor actions in Drosophila feeding
title_full Mechanosensory circuits coordinate two opposing motor actions in Drosophila feeding
title_fullStr Mechanosensory circuits coordinate two opposing motor actions in Drosophila feeding
title_full_unstemmed Mechanosensory circuits coordinate two opposing motor actions in Drosophila feeding
title_short Mechanosensory circuits coordinate two opposing motor actions in Drosophila feeding
title_sort mechanosensory circuits coordinate two opposing motor actions in drosophila feeding
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6531006/
https://www.ncbi.nlm.nih.gov/pubmed/31131327
http://dx.doi.org/10.1126/sciadv.aaw5141
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