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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
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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 |
format | Online Article Text |
id | pubmed-4786431 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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