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Modulation of Drosophila post-feeding physiology and behavior by the neuropeptide leucokinin
Behavior and physiology are orchestrated by neuropeptides acting as central neuromodulators and circulating hormones. An outstanding question is how these neuropeptides function to coordinate complex and competing behaviors. In Drosophila, the neuropeptide leucokinin (LK) modulates diverse functions...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245514/ https://www.ncbi.nlm.nih.gov/pubmed/30457986 http://dx.doi.org/10.1371/journal.pgen.1007767 |
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author | Zandawala, Meet Yurgel, Maria E. Texada, Michael J. Liao, Sifang Rewitz, Kim F. Keene, Alex C. Nässel, Dick R. |
author_facet | Zandawala, Meet Yurgel, Maria E. Texada, Michael J. Liao, Sifang Rewitz, Kim F. Keene, Alex C. Nässel, Dick R. |
author_sort | Zandawala, Meet |
collection | PubMed |
description | Behavior and physiology are orchestrated by neuropeptides acting as central neuromodulators and circulating hormones. An outstanding question is how these neuropeptides function to coordinate complex and competing behaviors. In Drosophila, the neuropeptide leucokinin (LK) modulates diverse functions, but mechanisms underlying these complex interactions remain poorly understood. As a first step towards understanding these mechanisms, we delineated LK circuitry that governs various aspects of post-feeding physiology and behavior. We found that impaired LK signaling in Lk and Lk receptor (Lkr) mutants affects diverse but coordinated processes, including regulation of stress, water homeostasis, feeding, locomotor activity, and metabolic rate. Next, we sought to define the populations of LK neurons that contribute to the different aspects of this physiology. We find that the calcium activity in abdominal ganglia LK neurons (ABLKs), but not in the two sets of brain neurons, increases specifically following water consumption, suggesting that ABLKs regulate water homeostasis and its associated physiology. To identify targets of LK peptide, we mapped the distribution of Lkr expression, mined a brain single-cell transcriptome dataset for genes coexpressed with Lkr, and identified synaptic partners of LK neurons. Lkr expression in the brain insulin-producing cells (IPCs), gut, renal tubules and chemosensory cells, correlates well with regulatory roles detected in the Lk and Lkr mutants. Furthermore, these mutants and flies with targeted knockdown of Lkr in IPCs displayed altered expression of insulin-like peptides (DILPs) and transcripts in IPCs and increased starvation resistance. Thus, some effects of LK signaling appear to occur via DILP action. Collectively, our data suggest that the three sets of LK neurons have different targets, but modulate the establishment of post-prandial homeostasis by regulating distinct physiological processes and behaviors such as diuresis, metabolism, organismal activity and insulin signaling. These findings provide a platform for investigating feeding-related neuroendocrine regulation of vital behavior and physiology. |
format | Online Article Text |
id | pubmed-6245514 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-62455142018-12-01 Modulation of Drosophila post-feeding physiology and behavior by the neuropeptide leucokinin Zandawala, Meet Yurgel, Maria E. Texada, Michael J. Liao, Sifang Rewitz, Kim F. Keene, Alex C. Nässel, Dick R. PLoS Genet Research Article Behavior and physiology are orchestrated by neuropeptides acting as central neuromodulators and circulating hormones. An outstanding question is how these neuropeptides function to coordinate complex and competing behaviors. In Drosophila, the neuropeptide leucokinin (LK) modulates diverse functions, but mechanisms underlying these complex interactions remain poorly understood. As a first step towards understanding these mechanisms, we delineated LK circuitry that governs various aspects of post-feeding physiology and behavior. We found that impaired LK signaling in Lk and Lk receptor (Lkr) mutants affects diverse but coordinated processes, including regulation of stress, water homeostasis, feeding, locomotor activity, and metabolic rate. Next, we sought to define the populations of LK neurons that contribute to the different aspects of this physiology. We find that the calcium activity in abdominal ganglia LK neurons (ABLKs), but not in the two sets of brain neurons, increases specifically following water consumption, suggesting that ABLKs regulate water homeostasis and its associated physiology. To identify targets of LK peptide, we mapped the distribution of Lkr expression, mined a brain single-cell transcriptome dataset for genes coexpressed with Lkr, and identified synaptic partners of LK neurons. Lkr expression in the brain insulin-producing cells (IPCs), gut, renal tubules and chemosensory cells, correlates well with regulatory roles detected in the Lk and Lkr mutants. Furthermore, these mutants and flies with targeted knockdown of Lkr in IPCs displayed altered expression of insulin-like peptides (DILPs) and transcripts in IPCs and increased starvation resistance. Thus, some effects of LK signaling appear to occur via DILP action. Collectively, our data suggest that the three sets of LK neurons have different targets, but modulate the establishment of post-prandial homeostasis by regulating distinct physiological processes and behaviors such as diuresis, metabolism, organismal activity and insulin signaling. These findings provide a platform for investigating feeding-related neuroendocrine regulation of vital behavior and physiology. Public Library of Science 2018-11-20 /pmc/articles/PMC6245514/ /pubmed/30457986 http://dx.doi.org/10.1371/journal.pgen.1007767 Text en © 2018 Zandawala 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 Zandawala, Meet Yurgel, Maria E. Texada, Michael J. Liao, Sifang Rewitz, Kim F. Keene, Alex C. Nässel, Dick R. Modulation of Drosophila post-feeding physiology and behavior by the neuropeptide leucokinin |
title | Modulation of Drosophila post-feeding physiology and behavior by the neuropeptide leucokinin |
title_full | Modulation of Drosophila post-feeding physiology and behavior by the neuropeptide leucokinin |
title_fullStr | Modulation of Drosophila post-feeding physiology and behavior by the neuropeptide leucokinin |
title_full_unstemmed | Modulation of Drosophila post-feeding physiology and behavior by the neuropeptide leucokinin |
title_short | Modulation of Drosophila post-feeding physiology and behavior by the neuropeptide leucokinin |
title_sort | modulation of drosophila post-feeding physiology and behavior by the neuropeptide leucokinin |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245514/ https://www.ncbi.nlm.nih.gov/pubmed/30457986 http://dx.doi.org/10.1371/journal.pgen.1007767 |
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