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Definition of the estrogen negative feedback pathway controlling the GnRH pulse generator in female mice
The mechanisms underlying the homeostatic estrogen negative feedback pathway central to mammalian fertility have remained unresolved. Direct measurement of gonadotropin-releasing hormone (GnRH) pulse generator activity in freely behaving mice with GCaMP photometry demonstrated striking estradiol-dep...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9718805/ https://www.ncbi.nlm.nih.gov/pubmed/36460649 http://dx.doi.org/10.1038/s41467-022-35243-z |
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author | McQuillan, H. James Clarkson, Jenny Kauff, Alexia Han, Su Young Yip, Siew Hoong Cheong, Isaiah Porteous, Robert Heather, Alison K. Herbison, Allan E. |
author_facet | McQuillan, H. James Clarkson, Jenny Kauff, Alexia Han, Su Young Yip, Siew Hoong Cheong, Isaiah Porteous, Robert Heather, Alison K. Herbison, Allan E. |
author_sort | McQuillan, H. James |
collection | PubMed |
description | The mechanisms underlying the homeostatic estrogen negative feedback pathway central to mammalian fertility have remained unresolved. Direct measurement of gonadotropin-releasing hormone (GnRH) pulse generator activity in freely behaving mice with GCaMP photometry demonstrated striking estradiol-dependent plasticity in the frequency, duration, amplitude, and profile of pulse generator synchronization events. Mice with Cre-dependent deletion of ESR1 from all kisspeptin neurons exhibited pulse generator activity identical to that of ovariectomized wild-type mice. An in vivo CRISPR-Cas9 approach was used to knockdown ESR1 expression selectively in arcuate nucleus (ARN) kisspeptin neurons. Mice with >80% deletion of ESR1 in ARN kisspeptin neurons exhibited the ovariectomized pattern of GnRH pulse generator activity and high frequency LH pulses but with very low amplitude due to reduced responsiveness of the pituitary. Together, these studies demonstrate that estrogen utilizes ESR1 in ARN kisspeptin neurons to achieve estrogen negative feedback of the GnRH pulse generator in mice. |
format | Online Article Text |
id | pubmed-9718805 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-97188052022-12-04 Definition of the estrogen negative feedback pathway controlling the GnRH pulse generator in female mice McQuillan, H. James Clarkson, Jenny Kauff, Alexia Han, Su Young Yip, Siew Hoong Cheong, Isaiah Porteous, Robert Heather, Alison K. Herbison, Allan E. Nat Commun Article The mechanisms underlying the homeostatic estrogen negative feedback pathway central to mammalian fertility have remained unresolved. Direct measurement of gonadotropin-releasing hormone (GnRH) pulse generator activity in freely behaving mice with GCaMP photometry demonstrated striking estradiol-dependent plasticity in the frequency, duration, amplitude, and profile of pulse generator synchronization events. Mice with Cre-dependent deletion of ESR1 from all kisspeptin neurons exhibited pulse generator activity identical to that of ovariectomized wild-type mice. An in vivo CRISPR-Cas9 approach was used to knockdown ESR1 expression selectively in arcuate nucleus (ARN) kisspeptin neurons. Mice with >80% deletion of ESR1 in ARN kisspeptin neurons exhibited the ovariectomized pattern of GnRH pulse generator activity and high frequency LH pulses but with very low amplitude due to reduced responsiveness of the pituitary. Together, these studies demonstrate that estrogen utilizes ESR1 in ARN kisspeptin neurons to achieve estrogen negative feedback of the GnRH pulse generator in mice. Nature Publishing Group UK 2022-12-02 /pmc/articles/PMC9718805/ /pubmed/36460649 http://dx.doi.org/10.1038/s41467-022-35243-z 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 McQuillan, H. James Clarkson, Jenny Kauff, Alexia Han, Su Young Yip, Siew Hoong Cheong, Isaiah Porteous, Robert Heather, Alison K. Herbison, Allan E. Definition of the estrogen negative feedback pathway controlling the GnRH pulse generator in female mice |
title | Definition of the estrogen negative feedback pathway controlling the GnRH pulse generator in female mice |
title_full | Definition of the estrogen negative feedback pathway controlling the GnRH pulse generator in female mice |
title_fullStr | Definition of the estrogen negative feedback pathway controlling the GnRH pulse generator in female mice |
title_full_unstemmed | Definition of the estrogen negative feedback pathway controlling the GnRH pulse generator in female mice |
title_short | Definition of the estrogen negative feedback pathway controlling the GnRH pulse generator in female mice |
title_sort | definition of the estrogen negative feedback pathway controlling the gnrh pulse generator in female mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9718805/ https://www.ncbi.nlm.nih.gov/pubmed/36460649 http://dx.doi.org/10.1038/s41467-022-35243-z |
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