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Peptidergic signaling from clock neurons regulates reproductive dormancy in Drosophila melanogaster

With the approach of winter, many insects switch to an alternative protective developmental program called diapause. Drosophila melanogaster females overwinter as adults by inducing a reproductive arrest that is characterized by inhibition of ovarian development at previtellogenic stages. The insuli...

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Autores principales: Nagy, Dóra, Cusumano, Paola, Andreatta, Gabriele, Anduaga, Ane Martin, Hermann-Luibl, Christiane, Reinhard, Nils, Gesto, João, Wegener, Christian, Mazzotta, Gabriella, Rosato, Ezio, Kyriacou, Charalambos P., Helfrich-Förster, Charlotte, Costa, Rodolfo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6592559/
https://www.ncbi.nlm.nih.gov/pubmed/31194738
http://dx.doi.org/10.1371/journal.pgen.1008158
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author Nagy, Dóra
Cusumano, Paola
Andreatta, Gabriele
Anduaga, Ane Martin
Hermann-Luibl, Christiane
Reinhard, Nils
Gesto, João
Wegener, Christian
Mazzotta, Gabriella
Rosato, Ezio
Kyriacou, Charalambos P.
Helfrich-Förster, Charlotte
Costa, Rodolfo
author_facet Nagy, Dóra
Cusumano, Paola
Andreatta, Gabriele
Anduaga, Ane Martin
Hermann-Luibl, Christiane
Reinhard, Nils
Gesto, João
Wegener, Christian
Mazzotta, Gabriella
Rosato, Ezio
Kyriacou, Charalambos P.
Helfrich-Förster, Charlotte
Costa, Rodolfo
author_sort Nagy, Dóra
collection PubMed
description With the approach of winter, many insects switch to an alternative protective developmental program called diapause. Drosophila melanogaster females overwinter as adults by inducing a reproductive arrest that is characterized by inhibition of ovarian development at previtellogenic stages. The insulin producing cells (IPCs) are key regulators of this process, since they produce and release insulin-like peptides that act as diapause-antagonizing hormones. Here we show that in D. melanogaster two neuropeptides, Pigment Dispersing Factor (PDF) and short Neuropeptide F (sNPF) inhibit reproductive arrest, likely through modulation of the IPCs. In particular, genetic manipulations of the PDF-expressing neurons, which include the sNPF-producing small ventral Lateral Neurons (s-LN(v)s), modulated the levels of reproductive dormancy, suggesting the involvement of both neuropeptides. We expressed a genetically encoded cAMP sensor in the IPCs and challenged brain explants with synthetic PDF and sNPF. Bath applications of both neuropeptides increased cAMP levels in the IPCs, even more so when they were applied together, suggesting a synergistic effect. Bath application of sNPF additionally increased Ca(2+) levels in the IPCs. Our results indicate that PDF and sNPF inhibit reproductive dormancy by maintaining the IPCs in an active state.
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spelling pubmed-65925592019-07-05 Peptidergic signaling from clock neurons regulates reproductive dormancy in Drosophila melanogaster Nagy, Dóra Cusumano, Paola Andreatta, Gabriele Anduaga, Ane Martin Hermann-Luibl, Christiane Reinhard, Nils Gesto, João Wegener, Christian Mazzotta, Gabriella Rosato, Ezio Kyriacou, Charalambos P. Helfrich-Förster, Charlotte Costa, Rodolfo PLoS Genet Research Article With the approach of winter, many insects switch to an alternative protective developmental program called diapause. Drosophila melanogaster females overwinter as adults by inducing a reproductive arrest that is characterized by inhibition of ovarian development at previtellogenic stages. The insulin producing cells (IPCs) are key regulators of this process, since they produce and release insulin-like peptides that act as diapause-antagonizing hormones. Here we show that in D. melanogaster two neuropeptides, Pigment Dispersing Factor (PDF) and short Neuropeptide F (sNPF) inhibit reproductive arrest, likely through modulation of the IPCs. In particular, genetic manipulations of the PDF-expressing neurons, which include the sNPF-producing small ventral Lateral Neurons (s-LN(v)s), modulated the levels of reproductive dormancy, suggesting the involvement of both neuropeptides. We expressed a genetically encoded cAMP sensor in the IPCs and challenged brain explants with synthetic PDF and sNPF. Bath applications of both neuropeptides increased cAMP levels in the IPCs, even more so when they were applied together, suggesting a synergistic effect. Bath application of sNPF additionally increased Ca(2+) levels in the IPCs. Our results indicate that PDF and sNPF inhibit reproductive dormancy by maintaining the IPCs in an active state. Public Library of Science 2019-06-13 /pmc/articles/PMC6592559/ /pubmed/31194738 http://dx.doi.org/10.1371/journal.pgen.1008158 Text en © 2019 Nagy 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
Nagy, Dóra
Cusumano, Paola
Andreatta, Gabriele
Anduaga, Ane Martin
Hermann-Luibl, Christiane
Reinhard, Nils
Gesto, João
Wegener, Christian
Mazzotta, Gabriella
Rosato, Ezio
Kyriacou, Charalambos P.
Helfrich-Förster, Charlotte
Costa, Rodolfo
Peptidergic signaling from clock neurons regulates reproductive dormancy in Drosophila melanogaster
title Peptidergic signaling from clock neurons regulates reproductive dormancy in Drosophila melanogaster
title_full Peptidergic signaling from clock neurons regulates reproductive dormancy in Drosophila melanogaster
title_fullStr Peptidergic signaling from clock neurons regulates reproductive dormancy in Drosophila melanogaster
title_full_unstemmed Peptidergic signaling from clock neurons regulates reproductive dormancy in Drosophila melanogaster
title_short Peptidergic signaling from clock neurons regulates reproductive dormancy in Drosophila melanogaster
title_sort peptidergic signaling from clock neurons regulates reproductive dormancy in drosophila melanogaster
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6592559/
https://www.ncbi.nlm.nih.gov/pubmed/31194738
http://dx.doi.org/10.1371/journal.pgen.1008158
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