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Evolutionary origins of taste buds: phylogenetic analysis of purinergic neurotransmission in epithelial chemosensors

Taste buds are gustatory endorgans which use an uncommon purinergic signalling system to transmit information to afferent gustatory nerve fibres. In mammals, ATP is a crucial neurotransmitter released by the taste cells to activate the afferent nerve fibres. Taste buds in mammals display a character...

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Autores principales: Kirino, Masato, Parnes, Jason, Hansen, Anne, Kiyohara, Sadao, Finger, Thomas E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3718344/
https://www.ncbi.nlm.nih.gov/pubmed/23466675
http://dx.doi.org/10.1098/rsob.130015
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author Kirino, Masato
Parnes, Jason
Hansen, Anne
Kiyohara, Sadao
Finger, Thomas E.
author_facet Kirino, Masato
Parnes, Jason
Hansen, Anne
Kiyohara, Sadao
Finger, Thomas E.
author_sort Kirino, Masato
collection PubMed
description Taste buds are gustatory endorgans which use an uncommon purinergic signalling system to transmit information to afferent gustatory nerve fibres. In mammals, ATP is a crucial neurotransmitter released by the taste cells to activate the afferent nerve fibres. Taste buds in mammals display a characteristic, highly specific ecto-ATPase (NTPDase2) activity, suggesting a role in inactivation of the neurotransmitter. The purpose of this study was to test whether the presence of markers of purinergic signalling characterize taste buds in anamniote vertebrates and to test whether similar purinergic systems are employed by other exteroceptive chemosensory systems. The species examined include several teleosts, elasmobranchs, lampreys and hagfish, the last of which lacks vertebrate-type taste buds. For comparison, Schreiner organs of hagfish and solitary chemosensory cells (SCCs) of teleosts, both of which are epidermal chemosensory end organs, were also examined because they might be evolutionarily related to taste buds. Ecto-ATPase activity was evident in elongate cells in all fish taste buds, including teleosts, elasmobranchs and lampreys. Neither SCCs nor Schreiner organs show specific ecto-ATPase activity, suggesting that purinergic signalling is not crucial in those systems as it is for taste buds. These findings suggest that the taste system did not originate from SCCs but arose independently in early vertebrates.
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spelling pubmed-37183442013-07-26 Evolutionary origins of taste buds: phylogenetic analysis of purinergic neurotransmission in epithelial chemosensors Kirino, Masato Parnes, Jason Hansen, Anne Kiyohara, Sadao Finger, Thomas E. Open Biol Research Taste buds are gustatory endorgans which use an uncommon purinergic signalling system to transmit information to afferent gustatory nerve fibres. In mammals, ATP is a crucial neurotransmitter released by the taste cells to activate the afferent nerve fibres. Taste buds in mammals display a characteristic, highly specific ecto-ATPase (NTPDase2) activity, suggesting a role in inactivation of the neurotransmitter. The purpose of this study was to test whether the presence of markers of purinergic signalling characterize taste buds in anamniote vertebrates and to test whether similar purinergic systems are employed by other exteroceptive chemosensory systems. The species examined include several teleosts, elasmobranchs, lampreys and hagfish, the last of which lacks vertebrate-type taste buds. For comparison, Schreiner organs of hagfish and solitary chemosensory cells (SCCs) of teleosts, both of which are epidermal chemosensory end organs, were also examined because they might be evolutionarily related to taste buds. Ecto-ATPase activity was evident in elongate cells in all fish taste buds, including teleosts, elasmobranchs and lampreys. Neither SCCs nor Schreiner organs show specific ecto-ATPase activity, suggesting that purinergic signalling is not crucial in those systems as it is for taste buds. These findings suggest that the taste system did not originate from SCCs but arose independently in early vertebrates. The Royal Society 2013-03 /pmc/articles/PMC3718344/ /pubmed/23466675 http://dx.doi.org/10.1098/rsob.130015 Text en http://creativecommons.org/licenses/by/3.0/ © 2013 The Authors. Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/3.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Research
Kirino, Masato
Parnes, Jason
Hansen, Anne
Kiyohara, Sadao
Finger, Thomas E.
Evolutionary origins of taste buds: phylogenetic analysis of purinergic neurotransmission in epithelial chemosensors
title Evolutionary origins of taste buds: phylogenetic analysis of purinergic neurotransmission in epithelial chemosensors
title_full Evolutionary origins of taste buds: phylogenetic analysis of purinergic neurotransmission in epithelial chemosensors
title_fullStr Evolutionary origins of taste buds: phylogenetic analysis of purinergic neurotransmission in epithelial chemosensors
title_full_unstemmed Evolutionary origins of taste buds: phylogenetic analysis of purinergic neurotransmission in epithelial chemosensors
title_short Evolutionary origins of taste buds: phylogenetic analysis of purinergic neurotransmission in epithelial chemosensors
title_sort evolutionary origins of taste buds: phylogenetic analysis of purinergic neurotransmission in epithelial chemosensors
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3718344/
https://www.ncbi.nlm.nih.gov/pubmed/23466675
http://dx.doi.org/10.1098/rsob.130015
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