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Second messenger molecules have a limited spread in olfactory cilia

Odorants are detected by olfactory receptors on the sensory cilia of olfactory receptor cells (ORCs). These cylindrical cilia have a diameters of 100–200 nm, within which the components required for signal transduction by the adenylyl cyclase–cAMP system are located. The kinetics of odorant response...

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Autores principales: Takeuchi, Hiroko, Kurahashi, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6279364/
https://www.ncbi.nlm.nih.gov/pubmed/30352795
http://dx.doi.org/10.1085/jgp.201812126
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author Takeuchi, Hiroko
Kurahashi, Takashi
author_facet Takeuchi, Hiroko
Kurahashi, Takashi
author_sort Takeuchi, Hiroko
collection PubMed
description Odorants are detected by olfactory receptors on the sensory cilia of olfactory receptor cells (ORCs). These cylindrical cilia have a diameters of 100–200 nm, within which the components required for signal transduction by the adenylyl cyclase–cAMP system are located. The kinetics of odorant responses are determined by the lifetimes of active proteins as well as the production, diffusion, and extrusion/degradation of second messenger molecules (cAMP and Ca(2+)). However, there is limited information about the molecular kinetics of ORC responses, mostly because of the technical limitations involved in studying such narrow spaces and fine structures. In this study, using a combination of electrophysiology, photolysis of caged substances, and spot UV laser stimulation, we show that second messenger molecules work only in the vicinity of their site of generation in the olfactory cilia. Such limited spreading clearly explains a unique feature of ORCs, namely, the integer multiple of unitary events that they display in low Ca(2+) conditions. Although the small ORC uses cAMP and Ca(2+) for various functions in different regions of the cell, these substances seem to operate only in the compartment that has been activated by the appropriate stimulus. We also show that these substances remain in the same vicinity for a long time. This enables the ORC to amplify the odorant signal and extend the lifetime of Ca(2+)-dependent adaptation. Cytoplasmic buffers and extrusion/degradation systems seem to play a crucial role in limiting molecular spreading. In addition, binding sites on the cytoplasmic surface of the plasma membrane may limit molecular diffusion in such a narrow space because of the high surface/volume ratio. Such efficient energy conversion may also be broadly used in other biological systems that have not yet been subjected to systematic experiments.
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spelling pubmed-62793642019-06-03 Second messenger molecules have a limited spread in olfactory cilia Takeuchi, Hiroko Kurahashi, Takashi J Gen Physiol Research Articles Odorants are detected by olfactory receptors on the sensory cilia of olfactory receptor cells (ORCs). These cylindrical cilia have a diameters of 100–200 nm, within which the components required for signal transduction by the adenylyl cyclase–cAMP system are located. The kinetics of odorant responses are determined by the lifetimes of active proteins as well as the production, diffusion, and extrusion/degradation of second messenger molecules (cAMP and Ca(2+)). However, there is limited information about the molecular kinetics of ORC responses, mostly because of the technical limitations involved in studying such narrow spaces and fine structures. In this study, using a combination of electrophysiology, photolysis of caged substances, and spot UV laser stimulation, we show that second messenger molecules work only in the vicinity of their site of generation in the olfactory cilia. Such limited spreading clearly explains a unique feature of ORCs, namely, the integer multiple of unitary events that they display in low Ca(2+) conditions. Although the small ORC uses cAMP and Ca(2+) for various functions in different regions of the cell, these substances seem to operate only in the compartment that has been activated by the appropriate stimulus. We also show that these substances remain in the same vicinity for a long time. This enables the ORC to amplify the odorant signal and extend the lifetime of Ca(2+)-dependent adaptation. Cytoplasmic buffers and extrusion/degradation systems seem to play a crucial role in limiting molecular spreading. In addition, binding sites on the cytoplasmic surface of the plasma membrane may limit molecular diffusion in such a narrow space because of the high surface/volume ratio. Such efficient energy conversion may also be broadly used in other biological systems that have not yet been subjected to systematic experiments. Rockefeller University Press 2018-12-03 /pmc/articles/PMC6279364/ /pubmed/30352795 http://dx.doi.org/10.1085/jgp.201812126 Text en © 2018 Takeuchi and Kurahashi http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Research Articles
Takeuchi, Hiroko
Kurahashi, Takashi
Second messenger molecules have a limited spread in olfactory cilia
title Second messenger molecules have a limited spread in olfactory cilia
title_full Second messenger molecules have a limited spread in olfactory cilia
title_fullStr Second messenger molecules have a limited spread in olfactory cilia
title_full_unstemmed Second messenger molecules have a limited spread in olfactory cilia
title_short Second messenger molecules have a limited spread in olfactory cilia
title_sort second messenger molecules have a limited spread in olfactory cilia
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6279364/
https://www.ncbi.nlm.nih.gov/pubmed/30352795
http://dx.doi.org/10.1085/jgp.201812126
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