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In vivo imaging of the GnRH pulse generator reveals a temporal order of neuronal activation and synchronization during each pulse

A hypothalamic pulse generator located in the arcuate nucleus controls episodic release of gonadotropin-releasing hormone (GnRH) and luteinizing hormone (LH) and is essential for reproduction. Recent evidence suggests this generator is composed of arcuate “KNDy” cells, the abbreviation based on coex...

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Autores principales: Moore, Aleisha M., Coolen, Lique M., Lehman, Michael N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8833213/
https://www.ncbi.nlm.nih.gov/pubmed/35110409
http://dx.doi.org/10.1073/pnas.2117767119
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author Moore, Aleisha M.
Coolen, Lique M.
Lehman, Michael N.
author_facet Moore, Aleisha M.
Coolen, Lique M.
Lehman, Michael N.
author_sort Moore, Aleisha M.
collection PubMed
description A hypothalamic pulse generator located in the arcuate nucleus controls episodic release of gonadotropin-releasing hormone (GnRH) and luteinizing hormone (LH) and is essential for reproduction. Recent evidence suggests this generator is composed of arcuate “KNDy” cells, the abbreviation based on coexpression of kisspeptin, neurokinin B, and dynorphin. However, direct visual evidence of KNDy neuron activity at a single-cell level during a pulse is lacking. Here, we use in vivo calcium imaging in freely moving female mice to show that individual KNDy neurons are synchronously activated in an episodic manner, and these synchronized episodes always precede LH pulses. Furthermore, synchronization among KNDy cells occurs in a temporal order, with some subsets of KNDy cells serving as “leaders” and others as “followers” during each synchronized episode. These results reveal an unsuspected temporal organization of activation and synchronization within the GnRH pulse generator, suggesting that different subsets of KNDy neurons are activated at pulse onset than afterward during maintenance and eventual termination of each pulse. Further studies to distinguish KNDy “leader” from “follower” cells is likely to have important clinical significance, since regulation of pulsatile GnRH secretion is essential for normal reproduction and disrupted in pathological conditions such as polycystic ovary syndrome and hypothalamic amenorrhea.
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spelling pubmed-88332132022-08-02 In vivo imaging of the GnRH pulse generator reveals a temporal order of neuronal activation and synchronization during each pulse Moore, Aleisha M. Coolen, Lique M. Lehman, Michael N. Proc Natl Acad Sci U S A Biological Sciences A hypothalamic pulse generator located in the arcuate nucleus controls episodic release of gonadotropin-releasing hormone (GnRH) and luteinizing hormone (LH) and is essential for reproduction. Recent evidence suggests this generator is composed of arcuate “KNDy” cells, the abbreviation based on coexpression of kisspeptin, neurokinin B, and dynorphin. However, direct visual evidence of KNDy neuron activity at a single-cell level during a pulse is lacking. Here, we use in vivo calcium imaging in freely moving female mice to show that individual KNDy neurons are synchronously activated in an episodic manner, and these synchronized episodes always precede LH pulses. Furthermore, synchronization among KNDy cells occurs in a temporal order, with some subsets of KNDy cells serving as “leaders” and others as “followers” during each synchronized episode. These results reveal an unsuspected temporal organization of activation and synchronization within the GnRH pulse generator, suggesting that different subsets of KNDy neurons are activated at pulse onset than afterward during maintenance and eventual termination of each pulse. Further studies to distinguish KNDy “leader” from “follower” cells is likely to have important clinical significance, since regulation of pulsatile GnRH secretion is essential for normal reproduction and disrupted in pathological conditions such as polycystic ovary syndrome and hypothalamic amenorrhea. National Academy of Sciences 2022-02-02 2022-02-08 /pmc/articles/PMC8833213/ /pubmed/35110409 http://dx.doi.org/10.1073/pnas.2117767119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Moore, Aleisha M.
Coolen, Lique M.
Lehman, Michael N.
In vivo imaging of the GnRH pulse generator reveals a temporal order of neuronal activation and synchronization during each pulse
title In vivo imaging of the GnRH pulse generator reveals a temporal order of neuronal activation and synchronization during each pulse
title_full In vivo imaging of the GnRH pulse generator reveals a temporal order of neuronal activation and synchronization during each pulse
title_fullStr In vivo imaging of the GnRH pulse generator reveals a temporal order of neuronal activation and synchronization during each pulse
title_full_unstemmed In vivo imaging of the GnRH pulse generator reveals a temporal order of neuronal activation and synchronization during each pulse
title_short In vivo imaging of the GnRH pulse generator reveals a temporal order of neuronal activation and synchronization during each pulse
title_sort in vivo imaging of the gnrh pulse generator reveals a temporal order of neuronal activation and synchronization during each pulse
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8833213/
https://www.ncbi.nlm.nih.gov/pubmed/35110409
http://dx.doi.org/10.1073/pnas.2117767119
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AT lehmanmichaeln invivoimagingofthegnrhpulsegeneratorrevealsatemporalorderofneuronalactivationandsynchronizationduringeachpulse