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Tonic signaling from O(2) sensors sets neural circuit activity and behavioral state
Tonic receptors convey stimulus duration and intensity and are implicated in homeostatic control. However, how tonic homeostatic signals are generated, and how they reconfigure neural circuits and modify animal behavior is poorly understood. Here we show that C. elegans O(2)-sensing neurons are toni...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3564487/ https://www.ncbi.nlm.nih.gov/pubmed/22388961 http://dx.doi.org/10.1038/nn.3061 |
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author | Busch, Karl Emanuel Laurent, Patrick Soltesz, Zoltan Murphy, Robin Joseph Faivre, Olivier Hedwig, Berthold Thomas, Martin Smith, Heather L. de Bono, Mario |
author_facet | Busch, Karl Emanuel Laurent, Patrick Soltesz, Zoltan Murphy, Robin Joseph Faivre, Olivier Hedwig, Berthold Thomas, Martin Smith, Heather L. de Bono, Mario |
author_sort | Busch, Karl Emanuel |
collection | PubMed |
description | Tonic receptors convey stimulus duration and intensity and are implicated in homeostatic control. However, how tonic homeostatic signals are generated, and how they reconfigure neural circuits and modify animal behavior is poorly understood. Here we show that C. elegans O(2)-sensing neurons are tonic receptors that continuously signal ambient [O(2)] to set the animal’s behavioral state. Sustained signalling relies on a Ca(2+) relay involving L-type voltage-gated Ca(2+) channels, the ryanodine and the IP(3) receptors. Tonic activity evokes continuous neuropeptide release, which helps elicit the enduring behavioral state associated with high [O(2)]. Sustained O(2) receptor signalling is propagated to downstream neural circuits, including the hub interneuron RMG. O(2) receptors evoke similar locomotory states at particular [O(2)], regardless of previous d[O(2)]/dt. However, a phasic component of the URX receptors’ response to high d[O(2)]/dt, as well as tonic-to-phasic transformations in downstream interneurons, enable transient reorientation movements shaped by d[O(2)]/dt. Our results highlight how tonic homeostatic signals can generate both transient and enduring behavioral change. |
format | Online Article Text |
id | pubmed-3564487 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
record_format | MEDLINE/PubMed |
spelling | pubmed-35644872013-02-05 Tonic signaling from O(2) sensors sets neural circuit activity and behavioral state Busch, Karl Emanuel Laurent, Patrick Soltesz, Zoltan Murphy, Robin Joseph Faivre, Olivier Hedwig, Berthold Thomas, Martin Smith, Heather L. de Bono, Mario Nat Neurosci Article Tonic receptors convey stimulus duration and intensity and are implicated in homeostatic control. However, how tonic homeostatic signals are generated, and how they reconfigure neural circuits and modify animal behavior is poorly understood. Here we show that C. elegans O(2)-sensing neurons are tonic receptors that continuously signal ambient [O(2)] to set the animal’s behavioral state. Sustained signalling relies on a Ca(2+) relay involving L-type voltage-gated Ca(2+) channels, the ryanodine and the IP(3) receptors. Tonic activity evokes continuous neuropeptide release, which helps elicit the enduring behavioral state associated with high [O(2)]. Sustained O(2) receptor signalling is propagated to downstream neural circuits, including the hub interneuron RMG. O(2) receptors evoke similar locomotory states at particular [O(2)], regardless of previous d[O(2)]/dt. However, a phasic component of the URX receptors’ response to high d[O(2)]/dt, as well as tonic-to-phasic transformations in downstream interneurons, enable transient reorientation movements shaped by d[O(2)]/dt. Our results highlight how tonic homeostatic signals can generate both transient and enduring behavioral change. 2012-03-04 /pmc/articles/PMC3564487/ /pubmed/22388961 http://dx.doi.org/10.1038/nn.3061 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Busch, Karl Emanuel Laurent, Patrick Soltesz, Zoltan Murphy, Robin Joseph Faivre, Olivier Hedwig, Berthold Thomas, Martin Smith, Heather L. de Bono, Mario Tonic signaling from O(2) sensors sets neural circuit activity and behavioral state |
title | Tonic signaling from O(2) sensors sets neural circuit activity and behavioral state |
title_full | Tonic signaling from O(2) sensors sets neural circuit activity and behavioral state |
title_fullStr | Tonic signaling from O(2) sensors sets neural circuit activity and behavioral state |
title_full_unstemmed | Tonic signaling from O(2) sensors sets neural circuit activity and behavioral state |
title_short | Tonic signaling from O(2) sensors sets neural circuit activity and behavioral state |
title_sort | tonic signaling from o(2) sensors sets neural circuit activity and behavioral state |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3564487/ https://www.ncbi.nlm.nih.gov/pubmed/22388961 http://dx.doi.org/10.1038/nn.3061 |
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