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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2019
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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. |
format | Online Article Text |
id | pubmed-6531006 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
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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