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Male-female communication enhances release of extracellular vesicles leading to high fertility in Drosophila

The female reproductive tract (female-RT) must decipher the repertoire of molecular cues received from the male during copulation in order to activate and coordinate tract functionality necessary for high fertility. In Drosophila, this modulation is partially driven by spermathecal secretory cells (...

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Autores principales: Sanchez-Lopez, Javier Arturo, Twena, Shai, Apel, Ido, Kornhaeuser, Shani Chen, Chasnitsky, Michael, Miklosi, Andras G., Vega-Dominguez, Perla J., Shephard, Alex, Hefetz, Amir, Heifetz, Yael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9376107/
https://www.ncbi.nlm.nih.gov/pubmed/35963938
http://dx.doi.org/10.1038/s42003-022-03770-6
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author Sanchez-Lopez, Javier Arturo
Twena, Shai
Apel, Ido
Kornhaeuser, Shani Chen
Chasnitsky, Michael
Miklosi, Andras G.
Vega-Dominguez, Perla J.
Shephard, Alex
Hefetz, Amir
Heifetz, Yael
author_facet Sanchez-Lopez, Javier Arturo
Twena, Shai
Apel, Ido
Kornhaeuser, Shani Chen
Chasnitsky, Michael
Miklosi, Andras G.
Vega-Dominguez, Perla J.
Shephard, Alex
Hefetz, Amir
Heifetz, Yael
author_sort Sanchez-Lopez, Javier Arturo
collection PubMed
description The female reproductive tract (female-RT) must decipher the repertoire of molecular cues received from the male during copulation in order to activate and coordinate tract functionality necessary for high fertility. In Drosophila, this modulation is partially driven by spermathecal secretory cells (SSC). The SSC are a layer of cuboidal secretory glandular cells surrounding the spermatheca capsule where sperm is stored. It is unclear, however, how the SSC regulate the system’s activity. Here we show that mating activates the secretory machinery of the SSC. The SSC release a heterogeneous population of extracellular vesicles (EVs) which is involved in initiating and managing the increase in egg-laying, and possibly sperm storage. Moreover, sperm and male accessory gland proteins are essential for such mating-mediated SSC activity. Thus, mating regulates secretory/endocytic pathways required for trafficking of vesicles to SSC-female-RT target sites, which modulate and coordinate reproductive tract activity to achieve high fertility.
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spelling pubmed-93761072022-08-15 Male-female communication enhances release of extracellular vesicles leading to high fertility in Drosophila Sanchez-Lopez, Javier Arturo Twena, Shai Apel, Ido Kornhaeuser, Shani Chen Chasnitsky, Michael Miklosi, Andras G. Vega-Dominguez, Perla J. Shephard, Alex Hefetz, Amir Heifetz, Yael Commun Biol Article The female reproductive tract (female-RT) must decipher the repertoire of molecular cues received from the male during copulation in order to activate and coordinate tract functionality necessary for high fertility. In Drosophila, this modulation is partially driven by spermathecal secretory cells (SSC). The SSC are a layer of cuboidal secretory glandular cells surrounding the spermatheca capsule where sperm is stored. It is unclear, however, how the SSC regulate the system’s activity. Here we show that mating activates the secretory machinery of the SSC. The SSC release a heterogeneous population of extracellular vesicles (EVs) which is involved in initiating and managing the increase in egg-laying, and possibly sperm storage. Moreover, sperm and male accessory gland proteins are essential for such mating-mediated SSC activity. Thus, mating regulates secretory/endocytic pathways required for trafficking of vesicles to SSC-female-RT target sites, which modulate and coordinate reproductive tract activity to achieve high fertility. Nature Publishing Group UK 2022-08-13 /pmc/articles/PMC9376107/ /pubmed/35963938 http://dx.doi.org/10.1038/s42003-022-03770-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Sanchez-Lopez, Javier Arturo
Twena, Shai
Apel, Ido
Kornhaeuser, Shani Chen
Chasnitsky, Michael
Miklosi, Andras G.
Vega-Dominguez, Perla J.
Shephard, Alex
Hefetz, Amir
Heifetz, Yael
Male-female communication enhances release of extracellular vesicles leading to high fertility in Drosophila
title Male-female communication enhances release of extracellular vesicles leading to high fertility in Drosophila
title_full Male-female communication enhances release of extracellular vesicles leading to high fertility in Drosophila
title_fullStr Male-female communication enhances release of extracellular vesicles leading to high fertility in Drosophila
title_full_unstemmed Male-female communication enhances release of extracellular vesicles leading to high fertility in Drosophila
title_short Male-female communication enhances release of extracellular vesicles leading to high fertility in Drosophila
title_sort male-female communication enhances release of extracellular vesicles leading to high fertility in drosophila
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9376107/
https://www.ncbi.nlm.nih.gov/pubmed/35963938
http://dx.doi.org/10.1038/s42003-022-03770-6
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