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The molecular phenotype of kisspeptin neurons in the medial amygdala of female mice

Reproduction is regulated through the hypothalamic-pituitary-gonadal (HPG) axis, largely via the action of kisspeptin neurons in the hypothalamus. Importantly, Kiss1 neurons have been identified in other brain regions, including the medial amygdala (MeA). Though the MeA is implicated in regulating a...

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Autores principales: Hatcher, Katherine M., Costanza, Leah, Kauffman, Alexander S., Stephens, Shannon B. Z.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9951589/
https://www.ncbi.nlm.nih.gov/pubmed/36843592
http://dx.doi.org/10.3389/fendo.2023.1093592
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author Hatcher, Katherine M.
Costanza, Leah
Kauffman, Alexander S.
Stephens, Shannon B. Z.
author_facet Hatcher, Katherine M.
Costanza, Leah
Kauffman, Alexander S.
Stephens, Shannon B. Z.
author_sort Hatcher, Katherine M.
collection PubMed
description Reproduction is regulated through the hypothalamic-pituitary-gonadal (HPG) axis, largely via the action of kisspeptin neurons in the hypothalamus. Importantly, Kiss1 neurons have been identified in other brain regions, including the medial amygdala (MeA). Though the MeA is implicated in regulating aspects of both reproductive physiology and behavior, as well as non-reproductive processes, the functional roles of MeA Kiss1 neurons are largely unknown. Additionally, besides their stimulation by estrogen, little is known about how MeA Kiss1 neurons are regulated. Using a RiboTag mouse model in conjunction with RNA-seq, we examined the molecular profile of MeA Kiss1 neurons to identify transcripts that are co-expressed in MeA Kiss1 neurons of female mice and whether these transcripts are modulated by estradiol (E(2)) treatment. RNA-seq identified >13,800 gene transcripts co-expressed in female MeA Kiss1 neurons, including genes for neuropeptides and receptors implicated in reproduction, metabolism, and other neuroendocrine functions. Of the >13,800 genes co-expressed in MeA Kiss1 neurons, only 45 genes demonstrated significantly different expression levels due to E(2) treatment. Gene transcripts such as Kiss1, Gal, and Oxtr increased in response to E(2) treatment, while fewer transcripts, such as Esr1 and Cyp26b1, were downregulated by E(2). Dual RNAscope and immunohistochemistry was performed to validate co-expression of MeA Kiss1 with Cck and Cartpt. These results are the first to establish a profile of genes actively expressed by MeA Kiss1 neurons, including a subset of genes regulated by E(2), which provides a useful foundation for future investigations into the regulation and function of MeA Kiss1 neurons.
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spelling pubmed-99515892023-02-25 The molecular phenotype of kisspeptin neurons in the medial amygdala of female mice Hatcher, Katherine M. Costanza, Leah Kauffman, Alexander S. Stephens, Shannon B. Z. Front Endocrinol (Lausanne) Endocrinology Reproduction is regulated through the hypothalamic-pituitary-gonadal (HPG) axis, largely via the action of kisspeptin neurons in the hypothalamus. Importantly, Kiss1 neurons have been identified in other brain regions, including the medial amygdala (MeA). Though the MeA is implicated in regulating aspects of both reproductive physiology and behavior, as well as non-reproductive processes, the functional roles of MeA Kiss1 neurons are largely unknown. Additionally, besides their stimulation by estrogen, little is known about how MeA Kiss1 neurons are regulated. Using a RiboTag mouse model in conjunction with RNA-seq, we examined the molecular profile of MeA Kiss1 neurons to identify transcripts that are co-expressed in MeA Kiss1 neurons of female mice and whether these transcripts are modulated by estradiol (E(2)) treatment. RNA-seq identified >13,800 gene transcripts co-expressed in female MeA Kiss1 neurons, including genes for neuropeptides and receptors implicated in reproduction, metabolism, and other neuroendocrine functions. Of the >13,800 genes co-expressed in MeA Kiss1 neurons, only 45 genes demonstrated significantly different expression levels due to E(2) treatment. Gene transcripts such as Kiss1, Gal, and Oxtr increased in response to E(2) treatment, while fewer transcripts, such as Esr1 and Cyp26b1, were downregulated by E(2). Dual RNAscope and immunohistochemistry was performed to validate co-expression of MeA Kiss1 with Cck and Cartpt. These results are the first to establish a profile of genes actively expressed by MeA Kiss1 neurons, including a subset of genes regulated by E(2), which provides a useful foundation for future investigations into the regulation and function of MeA Kiss1 neurons. Frontiers Media S.A. 2023-02-10 /pmc/articles/PMC9951589/ /pubmed/36843592 http://dx.doi.org/10.3389/fendo.2023.1093592 Text en Copyright © 2023 Hatcher, Costanza, Kauffman and Stephens https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Hatcher, Katherine M.
Costanza, Leah
Kauffman, Alexander S.
Stephens, Shannon B. Z.
The molecular phenotype of kisspeptin neurons in the medial amygdala of female mice
title The molecular phenotype of kisspeptin neurons in the medial amygdala of female mice
title_full The molecular phenotype of kisspeptin neurons in the medial amygdala of female mice
title_fullStr The molecular phenotype of kisspeptin neurons in the medial amygdala of female mice
title_full_unstemmed The molecular phenotype of kisspeptin neurons in the medial amygdala of female mice
title_short The molecular phenotype of kisspeptin neurons in the medial amygdala of female mice
title_sort molecular phenotype of kisspeptin neurons in the medial amygdala of female mice
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9951589/
https://www.ncbi.nlm.nih.gov/pubmed/36843592
http://dx.doi.org/10.3389/fendo.2023.1093592
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