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Mechanosensory circuits coordinate two opposing motor actions in Drosophila feeding.


ABSTRACT: 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.

SUBMITTER: Zhou Y 

PROVIDER: S-EPMC6531006 | biostudies-literature | 2019 May

REPOSITORIES: biostudies-literature

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Mechanosensory circuits coordinate two opposing motor actions in <i>Drosophila</i> feeding.

Zhou Yao Y   Cao Li-Hui LH   Sui Xiu-Wen XW   Guo Xiao-Qing XQ   Luo Dong-Gen DG  

Science advances 20190522 5


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 <i>Drosophila</i> 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. Connect  ...[more]

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