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Synaptic communication mediates the assembly of a self-organizing circuit that controls reproduction
Migration of gonadotropin-releasing hormone (GnRH) neurons from their birthplace in the nasal placode to their hypothalamic destination is critical for vertebrate reproduction and species persistence. While their migration mode as individual GnRH neurons has been extensively studied, the role of GnR...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7895442/ https://www.ncbi.nlm.nih.gov/pubmed/33608269 http://dx.doi.org/10.1126/sciadv.abc8475 |
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author | Golan, M. Boulanger-Weill, J. Pinot, A. Fontanaud, P. Faucherre, A. Gajbhiye, D. S. Hollander-Cohen, L. Fiordelisio-Coll, T. Martin, A. O. Mollard, P. |
author_facet | Golan, M. Boulanger-Weill, J. Pinot, A. Fontanaud, P. Faucherre, A. Gajbhiye, D. S. Hollander-Cohen, L. Fiordelisio-Coll, T. Martin, A. O. Mollard, P. |
author_sort | Golan, M. |
collection | PubMed |
description | Migration of gonadotropin-releasing hormone (GnRH) neurons from their birthplace in the nasal placode to their hypothalamic destination is critical for vertebrate reproduction and species persistence. While their migration mode as individual GnRH neurons has been extensively studied, the role of GnRH-GnRH cell communication during migration remains largely unexplored. Here, we show in awake zebrafish larvae that migrating GnRH neurons pause at the nasal-forebrain junction and form clusters that act as interhemisphere neuronal ensembles. Within the ensembles, GnRH neurons create an isolated, spontaneously active circuit that is internally wired through monosynaptic glutamatergic synapses into which newborn GnRH neurons integrate before entering the brain. This initial phase of integration drives a phenotypic switch, which is essential for GnRH neurons to properly migrate toward their hypothalamic destination. Together, these experiments reveal a critical step for reproduction, which depends on synaptic communication between migrating GnRH neurons. |
format | Online Article Text |
id | pubmed-7895442 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-78954422021-02-26 Synaptic communication mediates the assembly of a self-organizing circuit that controls reproduction Golan, M. Boulanger-Weill, J. Pinot, A. Fontanaud, P. Faucherre, A. Gajbhiye, D. S. Hollander-Cohen, L. Fiordelisio-Coll, T. Martin, A. O. Mollard, P. Sci Adv Research Articles Migration of gonadotropin-releasing hormone (GnRH) neurons from their birthplace in the nasal placode to their hypothalamic destination is critical for vertebrate reproduction and species persistence. While their migration mode as individual GnRH neurons has been extensively studied, the role of GnRH-GnRH cell communication during migration remains largely unexplored. Here, we show in awake zebrafish larvae that migrating GnRH neurons pause at the nasal-forebrain junction and form clusters that act as interhemisphere neuronal ensembles. Within the ensembles, GnRH neurons create an isolated, spontaneously active circuit that is internally wired through monosynaptic glutamatergic synapses into which newborn GnRH neurons integrate before entering the brain. This initial phase of integration drives a phenotypic switch, which is essential for GnRH neurons to properly migrate toward their hypothalamic destination. Together, these experiments reveal a critical step for reproduction, which depends on synaptic communication between migrating GnRH neurons. American Association for the Advancement of Science 2021-02-19 /pmc/articles/PMC7895442/ /pubmed/33608269 http://dx.doi.org/10.1126/sciadv.abc8475 Text en Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/ https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Golan, M. Boulanger-Weill, J. Pinot, A. Fontanaud, P. Faucherre, A. Gajbhiye, D. S. Hollander-Cohen, L. Fiordelisio-Coll, T. Martin, A. O. Mollard, P. Synaptic communication mediates the assembly of a self-organizing circuit that controls reproduction |
title | Synaptic communication mediates the assembly of a self-organizing circuit that controls reproduction |
title_full | Synaptic communication mediates the assembly of a self-organizing circuit that controls reproduction |
title_fullStr | Synaptic communication mediates the assembly of a self-organizing circuit that controls reproduction |
title_full_unstemmed | Synaptic communication mediates the assembly of a self-organizing circuit that controls reproduction |
title_short | Synaptic communication mediates the assembly of a self-organizing circuit that controls reproduction |
title_sort | synaptic communication mediates the assembly of a self-organizing circuit that controls reproduction |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7895442/ https://www.ncbi.nlm.nih.gov/pubmed/33608269 http://dx.doi.org/10.1126/sciadv.abc8475 |
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