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TRPV channel-mediated calcium transients in nociceptor neurons are dispensable for avoidance behaviour
Animals need to sense and react to potentially dangerous environments. TRP ion channels participate in nociception, presumably via Ca(2+) influx, in most animal species. However, the relationship between ion permeation and animals’ nocifensive behaviour is unknown. Here we use an invertebrate animal...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4164786/ https://www.ncbi.nlm.nih.gov/pubmed/25178952 http://dx.doi.org/10.1038/ncomms5734 |
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author | Lindy, Amanda S. Parekh, Puja K. Zhu, Richard Kanju, Patrick Chintapalli, Sree V. Tsvilovskyy, Volodymyr Patterson, Randen L. Anishkin, Andriy van Rossum, Damian B. Liedtke, Wolfgang B. |
author_facet | Lindy, Amanda S. Parekh, Puja K. Zhu, Richard Kanju, Patrick Chintapalli, Sree V. Tsvilovskyy, Volodymyr Patterson, Randen L. Anishkin, Andriy van Rossum, Damian B. Liedtke, Wolfgang B. |
author_sort | Lindy, Amanda S. |
collection | PubMed |
description | Animals need to sense and react to potentially dangerous environments. TRP ion channels participate in nociception, presumably via Ca(2+) influx, in most animal species. However, the relationship between ion permeation and animals’ nocifensive behaviour is unknown. Here we use an invertebrate animal model with relevance for mammalian pain. We analyse the putative selectivity filter of OSM-9, a TRPV channel, in osmotic avoidance behaviour of Caenorhabditis elegans. Using mutagenized OSM-9 expressed in the head nociceptor neuron, ASH, we study nocifensive behaviour and Ca(2+) influx. Within the selectivity filter, M(601)-F(609), Y604G strongly reduces avoidance behaviour and eliminates Ca(2+) transients. Y604F also abolishes Ca(2+) transients in ASH, while sustaining avoidance behaviour, yet it disrupts behavioral plasticity. Homology modelling of the OSM-9 pore suggests that Y(604) may assume a scaffolding role. Thus, aromatic residues in the OSM-9 selectivity filter are critical for pain behaviour and ion permeation. These findings have relevance for understanding evolutionary roots of mammalian nociception. |
format | Online Article Text |
id | pubmed-4164786 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-41647862014-09-22 TRPV channel-mediated calcium transients in nociceptor neurons are dispensable for avoidance behaviour Lindy, Amanda S. Parekh, Puja K. Zhu, Richard Kanju, Patrick Chintapalli, Sree V. Tsvilovskyy, Volodymyr Patterson, Randen L. Anishkin, Andriy van Rossum, Damian B. Liedtke, Wolfgang B. Nat Commun Article Animals need to sense and react to potentially dangerous environments. TRP ion channels participate in nociception, presumably via Ca(2+) influx, in most animal species. However, the relationship between ion permeation and animals’ nocifensive behaviour is unknown. Here we use an invertebrate animal model with relevance for mammalian pain. We analyse the putative selectivity filter of OSM-9, a TRPV channel, in osmotic avoidance behaviour of Caenorhabditis elegans. Using mutagenized OSM-9 expressed in the head nociceptor neuron, ASH, we study nocifensive behaviour and Ca(2+) influx. Within the selectivity filter, M(601)-F(609), Y604G strongly reduces avoidance behaviour and eliminates Ca(2+) transients. Y604F also abolishes Ca(2+) transients in ASH, while sustaining avoidance behaviour, yet it disrupts behavioral plasticity. Homology modelling of the OSM-9 pore suggests that Y(604) may assume a scaffolding role. Thus, aromatic residues in the OSM-9 selectivity filter are critical for pain behaviour and ion permeation. These findings have relevance for understanding evolutionary roots of mammalian nociception. Nature Pub. Group 2014-09-02 /pmc/articles/PMC4164786/ /pubmed/25178952 http://dx.doi.org/10.1038/ncomms5734 Text en Copyright © 2014, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Article Lindy, Amanda S. Parekh, Puja K. Zhu, Richard Kanju, Patrick Chintapalli, Sree V. Tsvilovskyy, Volodymyr Patterson, Randen L. Anishkin, Andriy van Rossum, Damian B. Liedtke, Wolfgang B. TRPV channel-mediated calcium transients in nociceptor neurons are dispensable for avoidance behaviour |
title | TRPV channel-mediated calcium transients in nociceptor neurons are dispensable for avoidance behaviour |
title_full | TRPV channel-mediated calcium transients in nociceptor neurons are dispensable for avoidance behaviour |
title_fullStr | TRPV channel-mediated calcium transients in nociceptor neurons are dispensable for avoidance behaviour |
title_full_unstemmed | TRPV channel-mediated calcium transients in nociceptor neurons are dispensable for avoidance behaviour |
title_short | TRPV channel-mediated calcium transients in nociceptor neurons are dispensable for avoidance behaviour |
title_sort | trpv channel-mediated calcium transients in nociceptor neurons are dispensable for avoidance behaviour |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4164786/ https://www.ncbi.nlm.nih.gov/pubmed/25178952 http://dx.doi.org/10.1038/ncomms5734 |
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