Literature DB >> 30654923

Ionotropic Receptors Specify the Morphogenesis of Phasic Sensors Controlling Rapid Thermal Preference in Drosophila.

Gonzalo Budelli1, Lina Ni2, Cristina Berciu3, Lena van Giesen1, Zachary A Knecht1, Elaine C Chang1, Benjamin Kaminski4, Ana F Silbering5, Aravi Samuel6, Mason Klein7, Richard Benton5, Daniela Nicastro8, Paul A Garrity9.   

Abstract

Thermosensation is critical for avoiding thermal extremes and regulating body temperature. While thermosensors activated by noxious temperatures respond to hot or cold, many innocuous thermosensors exhibit robust baseline activity and lack discrete temperature thresholds, suggesting they are not simply warm and cool detectors. Here, we investigate how the aristal Cold Cells encode innocuous temperatures in Drosophila. We find they are not cold sensors but cooling-activated and warming-inhibited phasic thermosensors that operate similarly at warm and cool temperatures; we propose renaming them "Cooling Cells." Unexpectedly, Cooling Cell thermosensing does not require the previously reported Brivido Transient Receptor Potential (TRP) channels. Instead, three Ionotropic Receptors (IRs), IR21a, IR25a, and IR93a, specify both the unique structure of Cooling Cell cilia endings and their thermosensitivity. Behaviorally, Cooling Cells promote both warm and cool avoidance. These findings reveal a morphogenetic role for IRs and demonstrate the central role of phasic thermosensing in innocuous thermosensation. VIDEO ABSTRACT.
Copyright © 2018 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Ir21a; Ir25a; Ir93a; iGluR; ionotropic receptor; morphogenesis; sensory neuron; temperature; thermoreceptor; thermosensation

Mesh:

Substances:

Year:  2019        PMID: 30654923      PMCID: PMC6709853          DOI: 10.1016/j.neuron.2018.12.022

Source DB:  PubMed          Journal:  Neuron        ISSN: 0896-6273            Impact factor:   17.173


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