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Octopamine neuron dependent aggression requires dVGLUT from dual-transmitting neurons
Neuromodulators such as monoamines are often expressed in neurons that also release at least one fast-acting neurotransmitter. The release of a combination of transmitters provides both “classical” and “modulatory” signals that could produce diverse and/or complementary effects in associated circuit...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7059954/ https://www.ncbi.nlm.nih.gov/pubmed/32097408 http://dx.doi.org/10.1371/journal.pgen.1008609 |
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author | Sherer, Lewis M. Catudio Garrett, Elizabeth Morgan, Hannah R. Brewer, Edmond D. Sirrs, Lucy A. Shearin, Harold K. Williams, Jessica L. McCabe, Brian D. Stowers, R. Steven Certel, Sarah J. |
author_facet | Sherer, Lewis M. Catudio Garrett, Elizabeth Morgan, Hannah R. Brewer, Edmond D. Sirrs, Lucy A. Shearin, Harold K. Williams, Jessica L. McCabe, Brian D. Stowers, R. Steven Certel, Sarah J. |
author_sort | Sherer, Lewis M. |
collection | PubMed |
description | Neuromodulators such as monoamines are often expressed in neurons that also release at least one fast-acting neurotransmitter. The release of a combination of transmitters provides both “classical” and “modulatory” signals that could produce diverse and/or complementary effects in associated circuits. Here, we establish that the majority of Drosophila octopamine (OA) neurons are also glutamatergic and identify the individual contributions of each neurotransmitter on sex-specific behaviors. Males without OA display low levels of aggression and high levels of inter-male courtship. Males deficient for dVGLUT solely in OA-glutamate neurons (OGNs) also exhibit a reduction in aggression, but without a concurrent increase in inter-male courtship. Within OGNs, a portion of VMAT and dVGLUT puncta differ in localization suggesting spatial differences in OA signaling. Our findings establish a previously undetermined role for dVGLUT in OA neurons and suggests that glutamate uncouples aggression from OA-dependent courtship-related behavior. These results indicate that dual neurotransmission can increase the efficacy of individual neurotransmitters while maintaining unique functions within a multi-functional social behavior neuronal network. |
format | Online Article Text |
id | pubmed-7059954 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-70599542020-03-12 Octopamine neuron dependent aggression requires dVGLUT from dual-transmitting neurons Sherer, Lewis M. Catudio Garrett, Elizabeth Morgan, Hannah R. Brewer, Edmond D. Sirrs, Lucy A. Shearin, Harold K. Williams, Jessica L. McCabe, Brian D. Stowers, R. Steven Certel, Sarah J. PLoS Genet Research Article Neuromodulators such as monoamines are often expressed in neurons that also release at least one fast-acting neurotransmitter. The release of a combination of transmitters provides both “classical” and “modulatory” signals that could produce diverse and/or complementary effects in associated circuits. Here, we establish that the majority of Drosophila octopamine (OA) neurons are also glutamatergic and identify the individual contributions of each neurotransmitter on sex-specific behaviors. Males without OA display low levels of aggression and high levels of inter-male courtship. Males deficient for dVGLUT solely in OA-glutamate neurons (OGNs) also exhibit a reduction in aggression, but without a concurrent increase in inter-male courtship. Within OGNs, a portion of VMAT and dVGLUT puncta differ in localization suggesting spatial differences in OA signaling. Our findings establish a previously undetermined role for dVGLUT in OA neurons and suggests that glutamate uncouples aggression from OA-dependent courtship-related behavior. These results indicate that dual neurotransmission can increase the efficacy of individual neurotransmitters while maintaining unique functions within a multi-functional social behavior neuronal network. Public Library of Science 2020-02-25 /pmc/articles/PMC7059954/ /pubmed/32097408 http://dx.doi.org/10.1371/journal.pgen.1008609 Text en © 2020 Sherer 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Sherer, Lewis M. Catudio Garrett, Elizabeth Morgan, Hannah R. Brewer, Edmond D. Sirrs, Lucy A. Shearin, Harold K. Williams, Jessica L. McCabe, Brian D. Stowers, R. Steven Certel, Sarah J. Octopamine neuron dependent aggression requires dVGLUT from dual-transmitting neurons |
title | Octopamine neuron dependent aggression requires dVGLUT from dual-transmitting neurons |
title_full | Octopamine neuron dependent aggression requires dVGLUT from dual-transmitting neurons |
title_fullStr | Octopamine neuron dependent aggression requires dVGLUT from dual-transmitting neurons |
title_full_unstemmed | Octopamine neuron dependent aggression requires dVGLUT from dual-transmitting neurons |
title_short | Octopamine neuron dependent aggression requires dVGLUT from dual-transmitting neurons |
title_sort | octopamine neuron dependent aggression requires dvglut from dual-transmitting neurons |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7059954/ https://www.ncbi.nlm.nih.gov/pubmed/32097408 http://dx.doi.org/10.1371/journal.pgen.1008609 |
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