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Identification of a Drosophila Glucose Receptor Using Ca(2+) Imaging of Single Chemosensory Neurons
Evaluation of food compounds by chemosensory cells is essential for animals to make appropriate feeding decisions. In the fruit fly Drosophila melanogaster, structurally diverse chemicals are detected by multimeric receptors composed of members of a large family of Gustatory receptor (Gr) proteins....
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3571953/ https://www.ncbi.nlm.nih.gov/pubmed/23418550 http://dx.doi.org/10.1371/journal.pone.0056304 |
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author | Miyamoto, Tetsuya Chen, Yan Slone, Jesse Amrein, Hubert |
author_facet | Miyamoto, Tetsuya Chen, Yan Slone, Jesse Amrein, Hubert |
author_sort | Miyamoto, Tetsuya |
collection | PubMed |
description | Evaluation of food compounds by chemosensory cells is essential for animals to make appropriate feeding decisions. In the fruit fly Drosophila melanogaster, structurally diverse chemicals are detected by multimeric receptors composed of members of a large family of Gustatory receptor (Gr) proteins. Putative sugar and bitter receptors are expressed in distinct subsets of Gustatory Receptor Neurons (GRN) of taste sensilla, thereby assigning distinct taste qualities to sugars and bitter tasting compounds, respectively. Here we report a Ca(2+) imaging method that allows association of ligand-mediated responses to a single GRN. We find that different sweet neurons exhibit distinct response profiles when stimulated with various sugars, and likewise, different bitter neurons exhibit distinct response profiles when stimulated with a set of bitter chemicals. These observations suggest that individual neurons within a taste modality are represented by distinct repertoires of sweet and bitter taste receptors, respectively. Furthermore, we employed this novel method to identify glucose as the primary ligand for the sugar receptor Gr61a, which is not only expressed in sweet sensing neurons of classical chemosensory sensilla, but also in two supersensitive neurons of atypical taste sensilla. Thus, single cell Ca(2+) imaging can be employed as a powerful tool to identify ligands for orphan Gr proteins. |
format | Online Article Text |
id | pubmed-3571953 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-35719532013-02-15 Identification of a Drosophila Glucose Receptor Using Ca(2+) Imaging of Single Chemosensory Neurons Miyamoto, Tetsuya Chen, Yan Slone, Jesse Amrein, Hubert PLoS One Research Article Evaluation of food compounds by chemosensory cells is essential for animals to make appropriate feeding decisions. In the fruit fly Drosophila melanogaster, structurally diverse chemicals are detected by multimeric receptors composed of members of a large family of Gustatory receptor (Gr) proteins. Putative sugar and bitter receptors are expressed in distinct subsets of Gustatory Receptor Neurons (GRN) of taste sensilla, thereby assigning distinct taste qualities to sugars and bitter tasting compounds, respectively. Here we report a Ca(2+) imaging method that allows association of ligand-mediated responses to a single GRN. We find that different sweet neurons exhibit distinct response profiles when stimulated with various sugars, and likewise, different bitter neurons exhibit distinct response profiles when stimulated with a set of bitter chemicals. These observations suggest that individual neurons within a taste modality are represented by distinct repertoires of sweet and bitter taste receptors, respectively. Furthermore, we employed this novel method to identify glucose as the primary ligand for the sugar receptor Gr61a, which is not only expressed in sweet sensing neurons of classical chemosensory sensilla, but also in two supersensitive neurons of atypical taste sensilla. Thus, single cell Ca(2+) imaging can be employed as a powerful tool to identify ligands for orphan Gr proteins. Public Library of Science 2013-02-13 /pmc/articles/PMC3571953/ /pubmed/23418550 http://dx.doi.org/10.1371/journal.pone.0056304 Text en © 2013 Miyamoto et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Miyamoto, Tetsuya Chen, Yan Slone, Jesse Amrein, Hubert Identification of a Drosophila Glucose Receptor Using Ca(2+) Imaging of Single Chemosensory Neurons |
title | Identification of a Drosophila Glucose Receptor Using Ca(2+) Imaging of Single Chemosensory Neurons |
title_full | Identification of a Drosophila Glucose Receptor Using Ca(2+) Imaging of Single Chemosensory Neurons |
title_fullStr | Identification of a Drosophila Glucose Receptor Using Ca(2+) Imaging of Single Chemosensory Neurons |
title_full_unstemmed | Identification of a Drosophila Glucose Receptor Using Ca(2+) Imaging of Single Chemosensory Neurons |
title_short | Identification of a Drosophila Glucose Receptor Using Ca(2+) Imaging of Single Chemosensory Neurons |
title_sort | identification of a drosophila glucose receptor using ca(2+) imaging of single chemosensory neurons |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3571953/ https://www.ncbi.nlm.nih.gov/pubmed/23418550 http://dx.doi.org/10.1371/journal.pone.0056304 |
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