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Metamorphosis of an identified serotonergic neuron in the Drosophila olfactory system
BACKGROUND: Odors are detected by sensory neurons that carry information to the olfactory lobe where they connect to projection neurons and local interneurons in glomeruli: anatomically well-characterized structures that collect, integrate and relay information to higher centers. Recent studies have...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2007
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2129096/ https://www.ncbi.nlm.nih.gov/pubmed/17958902 http://dx.doi.org/10.1186/1749-8104-2-20 |
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author | Roy, Bidisha Singh, Ajeet P Shetty, Chetak Chaudhary, Varun North, Annemarie Landgraf, Matthias VijayRaghavan, K Rodrigues, Veronica |
author_facet | Roy, Bidisha Singh, Ajeet P Shetty, Chetak Chaudhary, Varun North, Annemarie Landgraf, Matthias VijayRaghavan, K Rodrigues, Veronica |
author_sort | Roy, Bidisha |
collection | PubMed |
description | BACKGROUND: Odors are detected by sensory neurons that carry information to the olfactory lobe where they connect to projection neurons and local interneurons in glomeruli: anatomically well-characterized structures that collect, integrate and relay information to higher centers. Recent studies have revealed that the sensitivity of such networks can be modulated by wide-field feedback neurons. The connectivity and function of such feedback neurons are themselves subject to alteration by external cues, such as hormones, stress, or experience. Very little is known about how this class of central neurons changes its anatomical properties to perform functions in altered developmental contexts. A mechanistic understanding of how central neurons change their anatomy to meet new functional requirements will benefit greatly from the establishment of a model preparation where cellular and molecular changes can be examined in an identified central neuron. RESULTS: In this study, we examine a wide-field serotonergic neuron in the Drosophila olfactory pathway and map the dramatic changes that it undergoes from larva to adult. We show that expression of a dominant-negative form of the ecdysterone receptor prevents remodeling. We further use different transgenic constructs to silence neuronal activity and report defects in the morphology of the adult-specific dendritic trees. The branching of the presynaptic axonal arbors is regulated by mechanisms that affect axon growth and retrograde transport. The neuron develops its normal morphology in the absence of sensory input to the antennal lobe, or of the mushroom bodies. However, ablation of its presumptive postsynaptic partners, the projection neurons and/or local interneurons, affects the growth and branching of terminal arbors. CONCLUSION: Our studies establish a cellular system for studying remodeling of a central neuromodulatory feedback neuron and also identify key elements in this process. Understanding the morphogenesis of such neurons, which have been shown in other systems to modulate the sensitivity and directionality of response to odors, links anatomy to the development of olfactory behavior. |
format | Text |
id | pubmed-2129096 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-21290962007-12-11 Metamorphosis of an identified serotonergic neuron in the Drosophila olfactory system Roy, Bidisha Singh, Ajeet P Shetty, Chetak Chaudhary, Varun North, Annemarie Landgraf, Matthias VijayRaghavan, K Rodrigues, Veronica Neural Develop Research Article BACKGROUND: Odors are detected by sensory neurons that carry information to the olfactory lobe where they connect to projection neurons and local interneurons in glomeruli: anatomically well-characterized structures that collect, integrate and relay information to higher centers. Recent studies have revealed that the sensitivity of such networks can be modulated by wide-field feedback neurons. The connectivity and function of such feedback neurons are themselves subject to alteration by external cues, such as hormones, stress, or experience. Very little is known about how this class of central neurons changes its anatomical properties to perform functions in altered developmental contexts. A mechanistic understanding of how central neurons change their anatomy to meet new functional requirements will benefit greatly from the establishment of a model preparation where cellular and molecular changes can be examined in an identified central neuron. RESULTS: In this study, we examine a wide-field serotonergic neuron in the Drosophila olfactory pathway and map the dramatic changes that it undergoes from larva to adult. We show that expression of a dominant-negative form of the ecdysterone receptor prevents remodeling. We further use different transgenic constructs to silence neuronal activity and report defects in the morphology of the adult-specific dendritic trees. The branching of the presynaptic axonal arbors is regulated by mechanisms that affect axon growth and retrograde transport. The neuron develops its normal morphology in the absence of sensory input to the antennal lobe, or of the mushroom bodies. However, ablation of its presumptive postsynaptic partners, the projection neurons and/or local interneurons, affects the growth and branching of terminal arbors. CONCLUSION: Our studies establish a cellular system for studying remodeling of a central neuromodulatory feedback neuron and also identify key elements in this process. Understanding the morphogenesis of such neurons, which have been shown in other systems to modulate the sensitivity and directionality of response to odors, links anatomy to the development of olfactory behavior. BioMed Central 2007-10-24 /pmc/articles/PMC2129096/ /pubmed/17958902 http://dx.doi.org/10.1186/1749-8104-2-20 Text en Copyright © 2007 Roy et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Roy, Bidisha Singh, Ajeet P Shetty, Chetak Chaudhary, Varun North, Annemarie Landgraf, Matthias VijayRaghavan, K Rodrigues, Veronica Metamorphosis of an identified serotonergic neuron in the Drosophila olfactory system |
title | Metamorphosis of an identified serotonergic neuron in the Drosophila olfactory system |
title_full | Metamorphosis of an identified serotonergic neuron in the Drosophila olfactory system |
title_fullStr | Metamorphosis of an identified serotonergic neuron in the Drosophila olfactory system |
title_full_unstemmed | Metamorphosis of an identified serotonergic neuron in the Drosophila olfactory system |
title_short | Metamorphosis of an identified serotonergic neuron in the Drosophila olfactory system |
title_sort | metamorphosis of an identified serotonergic neuron in the drosophila olfactory system |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2129096/ https://www.ncbi.nlm.nih.gov/pubmed/17958902 http://dx.doi.org/10.1186/1749-8104-2-20 |
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