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Biophysical mechanisms underlying olfactory receptor neuron dynamics

Odor responses of olfactory receptor neurons (ORNs) exhibit complex dynamics. Using genetics and pharmacology, we show that these dynamics in Drosophila ORNs can be separated into sequential steps, corresponding to transduction and spike generation. Each of these steps contributes distinct dynamics....

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Detalles Bibliográficos
Autores principales: Nagel, Katherine I., Wilson, Rachel I.
Formato: Texto
Lenguaje:English
Publicado: 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3030680/
https://www.ncbi.nlm.nih.gov/pubmed/21217763
http://dx.doi.org/10.1038/nn.2725
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author Nagel, Katherine I.
Wilson, Rachel I.
author_facet Nagel, Katherine I.
Wilson, Rachel I.
author_sort Nagel, Katherine I.
collection PubMed
description Odor responses of olfactory receptor neurons (ORNs) exhibit complex dynamics. Using genetics and pharmacology, we show that these dynamics in Drosophila ORNs can be separated into sequential steps, corresponding to transduction and spike generation. Each of these steps contributes distinct dynamics. Transduction dynamics can be largely explained by a simple kinetic model of ligand-receptor interactions, together with an adaptive feedback mechanism that slows transduction onset. Spiking dynamics are well-described by a differentiating linear filter that is stereotyped across odors and cells. Genetic knock-down of sodium channels reshapes this filter, implying that it arises from the regulated balance of intrinsic conductances in ORNs. Complex responses can be understood as a consequence of how the stereotyped spike filter interacts with odor- and receptor-specific transduction dynamics. However, in the presence of rapidly fluctuating natural stimuli, spiking simply increases the speed and sensitivity of encoding.
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spelling pubmed-30306802011-08-01 Biophysical mechanisms underlying olfactory receptor neuron dynamics Nagel, Katherine I. Wilson, Rachel I. Nat Neurosci Article Odor responses of olfactory receptor neurons (ORNs) exhibit complex dynamics. Using genetics and pharmacology, we show that these dynamics in Drosophila ORNs can be separated into sequential steps, corresponding to transduction and spike generation. Each of these steps contributes distinct dynamics. Transduction dynamics can be largely explained by a simple kinetic model of ligand-receptor interactions, together with an adaptive feedback mechanism that slows transduction onset. Spiking dynamics are well-described by a differentiating linear filter that is stereotyped across odors and cells. Genetic knock-down of sodium channels reshapes this filter, implying that it arises from the regulated balance of intrinsic conductances in ORNs. Complex responses can be understood as a consequence of how the stereotyped spike filter interacts with odor- and receptor-specific transduction dynamics. However, in the presence of rapidly fluctuating natural stimuli, spiking simply increases the speed and sensitivity of encoding. 2011-01-09 2011-02 /pmc/articles/PMC3030680/ /pubmed/21217763 http://dx.doi.org/10.1038/nn.2725 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
Nagel, Katherine I.
Wilson, Rachel I.
Biophysical mechanisms underlying olfactory receptor neuron dynamics
title Biophysical mechanisms underlying olfactory receptor neuron dynamics
title_full Biophysical mechanisms underlying olfactory receptor neuron dynamics
title_fullStr Biophysical mechanisms underlying olfactory receptor neuron dynamics
title_full_unstemmed Biophysical mechanisms underlying olfactory receptor neuron dynamics
title_short Biophysical mechanisms underlying olfactory receptor neuron dynamics
title_sort biophysical mechanisms underlying olfactory receptor neuron dynamics
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3030680/
https://www.ncbi.nlm.nih.gov/pubmed/21217763
http://dx.doi.org/10.1038/nn.2725
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