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Genetic dissection of the different roles of hypothalamic kisspeptin neurons in regulating female reproduction
The brain regulates fertility through gonadotropin-releasing hormone (GnRH) neurons. Estradiol induces negative feedback on pulsatile GnRH/luteinizing hormone (LH) release and positive feedback generating preovulatory GnRH/LH surges. Negative and positive feedbacks are postulated to be mediated by k...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6491090/ https://www.ncbi.nlm.nih.gov/pubmed/30946012 http://dx.doi.org/10.7554/eLife.43999 |
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author | Wang, Luhong Vanacker, Charlotte Burger, Laura L Barnes, Tammy Shah, Yatrik M Myers, Martin G Moenter, Suzanne M |
author_facet | Wang, Luhong Vanacker, Charlotte Burger, Laura L Barnes, Tammy Shah, Yatrik M Myers, Martin G Moenter, Suzanne M |
author_sort | Wang, Luhong |
collection | PubMed |
description | The brain regulates fertility through gonadotropin-releasing hormone (GnRH) neurons. Estradiol induces negative feedback on pulsatile GnRH/luteinizing hormone (LH) release and positive feedback generating preovulatory GnRH/LH surges. Negative and positive feedbacks are postulated to be mediated by kisspeptin neurons in arcuate and anteroventral periventricular (AVPV) nuclei, respectively. Kisspeptin-specific ERα knockout mice exhibit disrupted LH pulses and surges. This knockout approach is neither location-specific nor temporally controlled. We utilized CRISPR-Cas9 to disrupt ERα in adulthood. Mice with ERα disruption in AVPV kisspeptin neurons have typical reproductive cycles but blunted LH surges, associated with decreased excitability of these neurons. Mice with ERα knocked down in arcuate kisspeptin neurons showed disrupted cyclicity, associated with increased glutamatergic transmission to these neurons. These observations suggest that activational effects of estradiol regulate surge generation and maintain cyclicity through AVPV and arcuate kisspeptin neurons, respectively, independent from its role in the development of hypothalamic kisspeptin neurons or puberty onset. |
format | Online Article Text |
id | pubmed-6491090 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-64910902019-05-02 Genetic dissection of the different roles of hypothalamic kisspeptin neurons in regulating female reproduction Wang, Luhong Vanacker, Charlotte Burger, Laura L Barnes, Tammy Shah, Yatrik M Myers, Martin G Moenter, Suzanne M eLife Neuroscience The brain regulates fertility through gonadotropin-releasing hormone (GnRH) neurons. Estradiol induces negative feedback on pulsatile GnRH/luteinizing hormone (LH) release and positive feedback generating preovulatory GnRH/LH surges. Negative and positive feedbacks are postulated to be mediated by kisspeptin neurons in arcuate and anteroventral periventricular (AVPV) nuclei, respectively. Kisspeptin-specific ERα knockout mice exhibit disrupted LH pulses and surges. This knockout approach is neither location-specific nor temporally controlled. We utilized CRISPR-Cas9 to disrupt ERα in adulthood. Mice with ERα disruption in AVPV kisspeptin neurons have typical reproductive cycles but blunted LH surges, associated with decreased excitability of these neurons. Mice with ERα knocked down in arcuate kisspeptin neurons showed disrupted cyclicity, associated with increased glutamatergic transmission to these neurons. These observations suggest that activational effects of estradiol regulate surge generation and maintain cyclicity through AVPV and arcuate kisspeptin neurons, respectively, independent from its role in the development of hypothalamic kisspeptin neurons or puberty onset. eLife Sciences Publications, Ltd 2019-04-04 /pmc/articles/PMC6491090/ /pubmed/30946012 http://dx.doi.org/10.7554/eLife.43999 Text en © 2019, Wang et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Wang, Luhong Vanacker, Charlotte Burger, Laura L Barnes, Tammy Shah, Yatrik M Myers, Martin G Moenter, Suzanne M Genetic dissection of the different roles of hypothalamic kisspeptin neurons in regulating female reproduction |
title | Genetic dissection of the different roles of hypothalamic kisspeptin neurons in regulating female reproduction |
title_full | Genetic dissection of the different roles of hypothalamic kisspeptin neurons in regulating female reproduction |
title_fullStr | Genetic dissection of the different roles of hypothalamic kisspeptin neurons in regulating female reproduction |
title_full_unstemmed | Genetic dissection of the different roles of hypothalamic kisspeptin neurons in regulating female reproduction |
title_short | Genetic dissection of the different roles of hypothalamic kisspeptin neurons in regulating female reproduction |
title_sort | genetic dissection of the different roles of hypothalamic kisspeptin neurons in regulating female reproduction |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6491090/ https://www.ncbi.nlm.nih.gov/pubmed/30946012 http://dx.doi.org/10.7554/eLife.43999 |
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