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Neuronal processing of noxious thermal stimuli mediated by dendritic Ca(2+) influx in Drosophila somatosensory neurons

Adequate responses to noxious stimuli causing tissue damages are essential for organismal survival. Class IV neurons in Drosophila larvae are polymodal nociceptors responsible for thermal, mechanical, and light sensation. Importantly, activation of Class IV provoked distinct avoidance behaviors, dep...

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Autores principales: Terada, Shin-Ichiro, Matsubara, Daisuke, Onodera, Koun, Matsuzaki, Masanori, Uemura, Tadashi, Usui, Tadao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4786431/
https://www.ncbi.nlm.nih.gov/pubmed/26880554
http://dx.doi.org/10.7554/eLife.12959
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author Terada, Shin-Ichiro
Matsubara, Daisuke
Onodera, Koun
Matsuzaki, Masanori
Uemura, Tadashi
Usui, Tadao
author_facet Terada, Shin-Ichiro
Matsubara, Daisuke
Onodera, Koun
Matsuzaki, Masanori
Uemura, Tadashi
Usui, Tadao
author_sort Terada, Shin-Ichiro
collection PubMed
description Adequate responses to noxious stimuli causing tissue damages are essential for organismal survival. Class IV neurons in Drosophila larvae are polymodal nociceptors responsible for thermal, mechanical, and light sensation. Importantly, activation of Class IV provoked distinct avoidance behaviors, depending on the inputs. We found that noxious thermal stimuli, but not blue light stimulation, caused a unique pattern of Class IV, which were composed of pauses after high-frequency spike trains and a large Ca(2+) rise in the dendrite (the Ca(2+) transient). Both these responses depended on two TRPA channels and the L-type voltage-gated calcium channel (L-VGCC), showing that the thermosensation provokes Ca(2+) influx. The precipitous fluctuation of firing rate in Class IV neurons enhanced the robust heat avoidance. We hypothesize that the Ca(2+) influx can be a key signal encoding a specific modality. DOI: http://dx.doi.org/10.7554/eLife.12959.001
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spelling pubmed-47864312016-03-17 Neuronal processing of noxious thermal stimuli mediated by dendritic Ca(2+) influx in Drosophila somatosensory neurons Terada, Shin-Ichiro Matsubara, Daisuke Onodera, Koun Matsuzaki, Masanori Uemura, Tadashi Usui, Tadao eLife Neuroscience Adequate responses to noxious stimuli causing tissue damages are essential for organismal survival. Class IV neurons in Drosophila larvae are polymodal nociceptors responsible for thermal, mechanical, and light sensation. Importantly, activation of Class IV provoked distinct avoidance behaviors, depending on the inputs. We found that noxious thermal stimuli, but not blue light stimulation, caused a unique pattern of Class IV, which were composed of pauses after high-frequency spike trains and a large Ca(2+) rise in the dendrite (the Ca(2+) transient). Both these responses depended on two TRPA channels and the L-type voltage-gated calcium channel (L-VGCC), showing that the thermosensation provokes Ca(2+) influx. The precipitous fluctuation of firing rate in Class IV neurons enhanced the robust heat avoidance. We hypothesize that the Ca(2+) influx can be a key signal encoding a specific modality. DOI: http://dx.doi.org/10.7554/eLife.12959.001 eLife Sciences Publications, Ltd 2016-02-15 /pmc/articles/PMC4786431/ /pubmed/26880554 http://dx.doi.org/10.7554/eLife.12959 Text en © 2016, Terada et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Terada, Shin-Ichiro
Matsubara, Daisuke
Onodera, Koun
Matsuzaki, Masanori
Uemura, Tadashi
Usui, Tadao
Neuronal processing of noxious thermal stimuli mediated by dendritic Ca(2+) influx in Drosophila somatosensory neurons
title Neuronal processing of noxious thermal stimuli mediated by dendritic Ca(2+) influx in Drosophila somatosensory neurons
title_full Neuronal processing of noxious thermal stimuli mediated by dendritic Ca(2+) influx in Drosophila somatosensory neurons
title_fullStr Neuronal processing of noxious thermal stimuli mediated by dendritic Ca(2+) influx in Drosophila somatosensory neurons
title_full_unstemmed Neuronal processing of noxious thermal stimuli mediated by dendritic Ca(2+) influx in Drosophila somatosensory neurons
title_short Neuronal processing of noxious thermal stimuli mediated by dendritic Ca(2+) influx in Drosophila somatosensory neurons
title_sort neuronal processing of noxious thermal stimuli mediated by dendritic ca(2+) influx in drosophila somatosensory neurons
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4786431/
https://www.ncbi.nlm.nih.gov/pubmed/26880554
http://dx.doi.org/10.7554/eLife.12959
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