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Nano-architecture of gustatory chemosensory bristles and trachea in Drosophila wings

In the Drosophila wing anterior margin, the dendrites of gustatory neurons occupy the interior of thin and long bristles that present tiny pores at their extremities. Many attempts to measure ligand-evoked currents in insect wing gustatory neurons have been unsuccessful for technical reasons. The fu...

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Autores principales: Valmalette, Jean Christophe, Raad, Hussein, Qiu, Nan, Ohara, Satoshi, Capovilla, Maria, Robichon, Alain
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4585653/
https://www.ncbi.nlm.nih.gov/pubmed/26381332
http://dx.doi.org/10.1038/srep14198
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author Valmalette, Jean Christophe
Raad, Hussein
Qiu, Nan
Ohara, Satoshi
Capovilla, Maria
Robichon, Alain
author_facet Valmalette, Jean Christophe
Raad, Hussein
Qiu, Nan
Ohara, Satoshi
Capovilla, Maria
Robichon, Alain
author_sort Valmalette, Jean Christophe
collection PubMed
description In the Drosophila wing anterior margin, the dendrites of gustatory neurons occupy the interior of thin and long bristles that present tiny pores at their extremities. Many attempts to measure ligand-evoked currents in insect wing gustatory neurons have been unsuccessful for technical reasons. The functions of this gustatory activity therefore remain elusive and controversial. To advance our knowledge on this understudied tissue, we investigated the architecture of the wing chemosensory bristles and wing trachea using Raman spectroscopy and fluorescence microscopy. We hypothesized that the wing gustatory hair, an open-ended capillary tube, and the wing trachea constitute biological systems similar to nano-porous materials. We present evidence that argues in favour of the existence of a layer or a bubble of air beneath the pore inside the gustatory hair. We demonstrate that these hollow hairs and wing tracheal tubes fulfil conditions for which the physics of fluids applied to open-ended capillaries and porous materials are relevant. We also document that the wing gustatory hair and tracheal architectures are capable of trapping volatile molecules from the environment, which might increase the efficiency of their spatial detection by way of wing vibrations or during flight.
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spelling pubmed-45856532015-09-29 Nano-architecture of gustatory chemosensory bristles and trachea in Drosophila wings Valmalette, Jean Christophe Raad, Hussein Qiu, Nan Ohara, Satoshi Capovilla, Maria Robichon, Alain Sci Rep Article In the Drosophila wing anterior margin, the dendrites of gustatory neurons occupy the interior of thin and long bristles that present tiny pores at their extremities. Many attempts to measure ligand-evoked currents in insect wing gustatory neurons have been unsuccessful for technical reasons. The functions of this gustatory activity therefore remain elusive and controversial. To advance our knowledge on this understudied tissue, we investigated the architecture of the wing chemosensory bristles and wing trachea using Raman spectroscopy and fluorescence microscopy. We hypothesized that the wing gustatory hair, an open-ended capillary tube, and the wing trachea constitute biological systems similar to nano-porous materials. We present evidence that argues in favour of the existence of a layer or a bubble of air beneath the pore inside the gustatory hair. We demonstrate that these hollow hairs and wing tracheal tubes fulfil conditions for which the physics of fluids applied to open-ended capillaries and porous materials are relevant. We also document that the wing gustatory hair and tracheal architectures are capable of trapping volatile molecules from the environment, which might increase the efficiency of their spatial detection by way of wing vibrations or during flight. Nature Publishing Group 2015-09-18 /pmc/articles/PMC4585653/ /pubmed/26381332 http://dx.doi.org/10.1038/srep14198 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Valmalette, Jean Christophe
Raad, Hussein
Qiu, Nan
Ohara, Satoshi
Capovilla, Maria
Robichon, Alain
Nano-architecture of gustatory chemosensory bristles and trachea in Drosophila wings
title Nano-architecture of gustatory chemosensory bristles and trachea in Drosophila wings
title_full Nano-architecture of gustatory chemosensory bristles and trachea in Drosophila wings
title_fullStr Nano-architecture of gustatory chemosensory bristles and trachea in Drosophila wings
title_full_unstemmed Nano-architecture of gustatory chemosensory bristles and trachea in Drosophila wings
title_short Nano-architecture of gustatory chemosensory bristles and trachea in Drosophila wings
title_sort nano-architecture of gustatory chemosensory bristles and trachea in drosophila wings
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4585653/
https://www.ncbi.nlm.nih.gov/pubmed/26381332
http://dx.doi.org/10.1038/srep14198
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