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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2021
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.
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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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