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Rapid threat assessment in the Drosophila thermosensory system
Neurons that participate in sensory processing often display “ON” responses, i.e., fire transiently at the onset of a stimulus. ON transients are widespread, perhaps universal to sensory coding, yet their function is not always well-understood. Here, we show that ON responses in the Drosophila therm...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10624821/ https://www.ncbi.nlm.nih.gov/pubmed/37923719 http://dx.doi.org/10.1038/s41467-023-42864-5 |
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author | Jouandet, Genevieve C. Alpert, Michael H. Simões, José Miguel Suhendra, Richard Frank, Dominic D. Levy, Joshua I. Para, Alessia Kath, William L. Gallio, Marco |
author_facet | Jouandet, Genevieve C. Alpert, Michael H. Simões, José Miguel Suhendra, Richard Frank, Dominic D. Levy, Joshua I. Para, Alessia Kath, William L. Gallio, Marco |
author_sort | Jouandet, Genevieve C. |
collection | PubMed |
description | Neurons that participate in sensory processing often display “ON” responses, i.e., fire transiently at the onset of a stimulus. ON transients are widespread, perhaps universal to sensory coding, yet their function is not always well-understood. Here, we show that ON responses in the Drosophila thermosensory system extrapolate the trajectory of temperature change, priming escape behavior if unsafe thermal conditions are imminent. First, we show that second-order thermosensory projection neurons (TPN-IIIs) and their Lateral Horn targets (TLHONs), display ON responses to thermal stimuli, independent of direction of change (heating or cooling) and of absolute temperature. Instead, they track the rate of temperature change, with TLHONs firing exclusively to rapid changes (>0.2 °C/s). Next, we use connectomics to track TLHONs’ output to descending neurons that control walking and escape, and modeling and genetic silencing to demonstrate how ON transients can flexibly amplify aversive responses to small thermal change. Our results suggest that, across sensory systems, ON transients may represent a general mechanism to systematically anticipate and respond to salient or dangerous conditions. |
format | Online Article Text |
id | pubmed-10624821 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-106248212023-11-05 Rapid threat assessment in the Drosophila thermosensory system Jouandet, Genevieve C. Alpert, Michael H. Simões, José Miguel Suhendra, Richard Frank, Dominic D. Levy, Joshua I. Para, Alessia Kath, William L. Gallio, Marco Nat Commun Article Neurons that participate in sensory processing often display “ON” responses, i.e., fire transiently at the onset of a stimulus. ON transients are widespread, perhaps universal to sensory coding, yet their function is not always well-understood. Here, we show that ON responses in the Drosophila thermosensory system extrapolate the trajectory of temperature change, priming escape behavior if unsafe thermal conditions are imminent. First, we show that second-order thermosensory projection neurons (TPN-IIIs) and their Lateral Horn targets (TLHONs), display ON responses to thermal stimuli, independent of direction of change (heating or cooling) and of absolute temperature. Instead, they track the rate of temperature change, with TLHONs firing exclusively to rapid changes (>0.2 °C/s). Next, we use connectomics to track TLHONs’ output to descending neurons that control walking and escape, and modeling and genetic silencing to demonstrate how ON transients can flexibly amplify aversive responses to small thermal change. Our results suggest that, across sensory systems, ON transients may represent a general mechanism to systematically anticipate and respond to salient or dangerous conditions. Nature Publishing Group UK 2023-11-03 /pmc/articles/PMC10624821/ /pubmed/37923719 http://dx.doi.org/10.1038/s41467-023-42864-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Jouandet, Genevieve C. Alpert, Michael H. Simões, José Miguel Suhendra, Richard Frank, Dominic D. Levy, Joshua I. Para, Alessia Kath, William L. Gallio, Marco Rapid threat assessment in the Drosophila thermosensory system |
title | Rapid threat assessment in the Drosophila thermosensory system |
title_full | Rapid threat assessment in the Drosophila thermosensory system |
title_fullStr | Rapid threat assessment in the Drosophila thermosensory system |
title_full_unstemmed | Rapid threat assessment in the Drosophila thermosensory system |
title_short | Rapid threat assessment in the Drosophila thermosensory system |
title_sort | rapid threat assessment in the drosophila thermosensory system |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10624821/ https://www.ncbi.nlm.nih.gov/pubmed/37923719 http://dx.doi.org/10.1038/s41467-023-42864-5 |
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