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Expression of a GABA(B )- Receptor in Olfactory Sensory Neurons of Sensilla trichodea on the Male Antenna of the Moth Heliothis virescens

In the olfactory pathway of Drosophila, a GABA(B) receptor mediated presynaptic gain control mechanism at the first synapse between olfactory sensory neurons (OSNs) and projection neurons has been suggested to play a critical role in setting the sensitivity and detection range of the sensory system....

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Autores principales: Pregitzer, Pablo, Schultze, Anna, Raming, Klaus, Breer, Heinz, Krieger, Jürgen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3729013/
https://www.ncbi.nlm.nih.gov/pubmed/23904795
http://dx.doi.org/10.7150/ijbs.6674
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author Pregitzer, Pablo
Schultze, Anna
Raming, Klaus
Breer, Heinz
Krieger, Jürgen
author_facet Pregitzer, Pablo
Schultze, Anna
Raming, Klaus
Breer, Heinz
Krieger, Jürgen
author_sort Pregitzer, Pablo
collection PubMed
description In the olfactory pathway of Drosophila, a GABA(B) receptor mediated presynaptic gain control mechanism at the first synapse between olfactory sensory neurons (OSNs) and projection neurons has been suggested to play a critical role in setting the sensitivity and detection range of the sensory system. To approach the question if such a mechanism may be realized in the pheromone recognition system of male moths in this study attempts were made to explore if moth's pheromone-responsive cells express a GABA(B)- receptor. Employing a combination of genome analysis, RT-PCR experiments and screening of an antennal cDNA library we have identified a cDNA which encodes the GABA(B)-R1 receptor of Heliothis virescens. Moreover, based on the HvirGABA(B)-R1 sequence we could predict a GABA(B)-R1 protein from genome sequences of the silkmoth Bombyx mori. To assess whether HvirGABA(B)-R1 is expressed in OSNs of male antenna we performed whole-mount in situ hybridization (WM-ISH) experiments. Several HvirGABA(B)-R1 positive cells were visualized under long sensilla trichodea, known to contain pheromone-responsive OSNs. In parallel it was shown that cells under long trichoid hairs were labelled with pheromone receptor specific probes. In addition, the HvirGABA(B)-R1 specific probe also labelled several cells under shorter olfactory sensilla, but never stained cells under mechanosensory/gustatory sensilla chaetica. Together, the results indicate that a GABA(B) receptor is expressed in pheromone-responsive OSNs of H. virescens and suggest a presynaptic gain control mechanism in the axon terminals of these cells.
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spelling pubmed-37290132013-07-31 Expression of a GABA(B )- Receptor in Olfactory Sensory Neurons of Sensilla trichodea on the Male Antenna of the Moth Heliothis virescens Pregitzer, Pablo Schultze, Anna Raming, Klaus Breer, Heinz Krieger, Jürgen Int J Biol Sci Research Paper In the olfactory pathway of Drosophila, a GABA(B) receptor mediated presynaptic gain control mechanism at the first synapse between olfactory sensory neurons (OSNs) and projection neurons has been suggested to play a critical role in setting the sensitivity and detection range of the sensory system. To approach the question if such a mechanism may be realized in the pheromone recognition system of male moths in this study attempts were made to explore if moth's pheromone-responsive cells express a GABA(B)- receptor. Employing a combination of genome analysis, RT-PCR experiments and screening of an antennal cDNA library we have identified a cDNA which encodes the GABA(B)-R1 receptor of Heliothis virescens. Moreover, based on the HvirGABA(B)-R1 sequence we could predict a GABA(B)-R1 protein from genome sequences of the silkmoth Bombyx mori. To assess whether HvirGABA(B)-R1 is expressed in OSNs of male antenna we performed whole-mount in situ hybridization (WM-ISH) experiments. Several HvirGABA(B)-R1 positive cells were visualized under long sensilla trichodea, known to contain pheromone-responsive OSNs. In parallel it was shown that cells under long trichoid hairs were labelled with pheromone receptor specific probes. In addition, the HvirGABA(B)-R1 specific probe also labelled several cells under shorter olfactory sensilla, but never stained cells under mechanosensory/gustatory sensilla chaetica. Together, the results indicate that a GABA(B) receptor is expressed in pheromone-responsive OSNs of H. virescens and suggest a presynaptic gain control mechanism in the axon terminals of these cells. Ivyspring International Publisher 2013-07-20 /pmc/articles/PMC3729013/ /pubmed/23904795 http://dx.doi.org/10.7150/ijbs.6674 Text en © Ivyspring International Publisher. This is an open-access article distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by-nc-nd/3.0/). Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited.
spellingShingle Research Paper
Pregitzer, Pablo
Schultze, Anna
Raming, Klaus
Breer, Heinz
Krieger, Jürgen
Expression of a GABA(B )- Receptor in Olfactory Sensory Neurons of Sensilla trichodea on the Male Antenna of the Moth Heliothis virescens
title Expression of a GABA(B )- Receptor in Olfactory Sensory Neurons of Sensilla trichodea on the Male Antenna of the Moth Heliothis virescens
title_full Expression of a GABA(B )- Receptor in Olfactory Sensory Neurons of Sensilla trichodea on the Male Antenna of the Moth Heliothis virescens
title_fullStr Expression of a GABA(B )- Receptor in Olfactory Sensory Neurons of Sensilla trichodea on the Male Antenna of the Moth Heliothis virescens
title_full_unstemmed Expression of a GABA(B )- Receptor in Olfactory Sensory Neurons of Sensilla trichodea on the Male Antenna of the Moth Heliothis virescens
title_short Expression of a GABA(B )- Receptor in Olfactory Sensory Neurons of Sensilla trichodea on the Male Antenna of the Moth Heliothis virescens
title_sort expression of a gaba(b )- receptor in olfactory sensory neurons of sensilla trichodea on the male antenna of the moth heliothis virescens
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3729013/
https://www.ncbi.nlm.nih.gov/pubmed/23904795
http://dx.doi.org/10.7150/ijbs.6674
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