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Co‐expression of the calcitonin receptor gene in the hypothalamic kisspeptin neurons in female rats
PURPOSE: Hypothalamic kisspeptin neurons are considered to play a critical role in regulating mammalian reproduction and integrating humoral and neuronal inputs that control gonadotropin‐releasing hormone (GnRH)/gonadotropin release. The present study aimed to investigate the upstream regulator cand...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5902471/ https://www.ncbi.nlm.nih.gov/pubmed/29692674 http://dx.doi.org/10.1002/rmb2.12085 |
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author | Assadullah, Ieda, Nahoko Kawai, Narumi Ishii, Hirotaka Ihara, Kunio Inoue, Naoko Uenoyama, Yoshihisa Tsukamura, Hiroko |
author_facet | Assadullah, Ieda, Nahoko Kawai, Narumi Ishii, Hirotaka Ihara, Kunio Inoue, Naoko Uenoyama, Yoshihisa Tsukamura, Hiroko |
author_sort | Assadullah, |
collection | PubMed |
description | PURPOSE: Hypothalamic kisspeptin neurons are considered to play a critical role in regulating mammalian reproduction and integrating humoral and neuronal inputs that control gonadotropin‐releasing hormone (GnRH)/gonadotropin release. The present study aimed to investigate the upstream regulator candidates for kisspeptin neurons. METHODS: Visualized kisspeptin neurons that were taken from the arcuate nucleus (ARC) of Kiss1‐tdTomato rats were subjected to next‐generation sequencing (NGS) analysis. In situ hybridization (ISH) for the calcitonin receptor gene (Calcr) was performed throughout the whole forebrain of ovariectomized wild‐type female rats that had been implanted with a negative feedback level of estrogen, because the Calcr expression was evident in the ARC kisspeptin neurons from the NGS analysis. Then, a double ISH was performed for the Calcr and kisspeptin gene (Kiss1) in the brain regions, containing either the anteroventral periventricular nucleus (AVPV) or ARC of the female rats. RESULTS: The NGS analysis revealed that the Calcr was highly expressed in the ARC kisspeptin neurons. It was found that the Calcr was co‐expressed in 12% and 22% of the Kiss1‐expressing cells in the ARC and AVPV, respectively. CONCLUSION: The present study suggests that calcitonin receptor signaling could be involved in the regulation of reproductive function through the direct control of the ARC and/or AVPV kisspeptin neurons, and then GnRH/gonadotropin release. |
format | Online Article Text |
id | pubmed-5902471 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-59024712018-04-24 Co‐expression of the calcitonin receptor gene in the hypothalamic kisspeptin neurons in female rats Assadullah, Ieda, Nahoko Kawai, Narumi Ishii, Hirotaka Ihara, Kunio Inoue, Naoko Uenoyama, Yoshihisa Tsukamura, Hiroko Reprod Med Biol Original Articles PURPOSE: Hypothalamic kisspeptin neurons are considered to play a critical role in regulating mammalian reproduction and integrating humoral and neuronal inputs that control gonadotropin‐releasing hormone (GnRH)/gonadotropin release. The present study aimed to investigate the upstream regulator candidates for kisspeptin neurons. METHODS: Visualized kisspeptin neurons that were taken from the arcuate nucleus (ARC) of Kiss1‐tdTomato rats were subjected to next‐generation sequencing (NGS) analysis. In situ hybridization (ISH) for the calcitonin receptor gene (Calcr) was performed throughout the whole forebrain of ovariectomized wild‐type female rats that had been implanted with a negative feedback level of estrogen, because the Calcr expression was evident in the ARC kisspeptin neurons from the NGS analysis. Then, a double ISH was performed for the Calcr and kisspeptin gene (Kiss1) in the brain regions, containing either the anteroventral periventricular nucleus (AVPV) or ARC of the female rats. RESULTS: The NGS analysis revealed that the Calcr was highly expressed in the ARC kisspeptin neurons. It was found that the Calcr was co‐expressed in 12% and 22% of the Kiss1‐expressing cells in the ARC and AVPV, respectively. CONCLUSION: The present study suggests that calcitonin receptor signaling could be involved in the regulation of reproductive function through the direct control of the ARC and/or AVPV kisspeptin neurons, and then GnRH/gonadotropin release. John Wiley and Sons Inc. 2018-03-11 /pmc/articles/PMC5902471/ /pubmed/29692674 http://dx.doi.org/10.1002/rmb2.12085 Text en © 2018 The Authors. Reproductive Medicine and Biology published by John Wiley & Sons Australia, Ltd on behalf of Japan Society for Reproductive Medicine. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Assadullah, Ieda, Nahoko Kawai, Narumi Ishii, Hirotaka Ihara, Kunio Inoue, Naoko Uenoyama, Yoshihisa Tsukamura, Hiroko Co‐expression of the calcitonin receptor gene in the hypothalamic kisspeptin neurons in female rats |
title | Co‐expression of the calcitonin receptor gene in the hypothalamic kisspeptin neurons in female rats |
title_full | Co‐expression of the calcitonin receptor gene in the hypothalamic kisspeptin neurons in female rats |
title_fullStr | Co‐expression of the calcitonin receptor gene in the hypothalamic kisspeptin neurons in female rats |
title_full_unstemmed | Co‐expression of the calcitonin receptor gene in the hypothalamic kisspeptin neurons in female rats |
title_short | Co‐expression of the calcitonin receptor gene in the hypothalamic kisspeptin neurons in female rats |
title_sort | co‐expression of the calcitonin receptor gene in the hypothalamic kisspeptin neurons in female rats |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5902471/ https://www.ncbi.nlm.nih.gov/pubmed/29692674 http://dx.doi.org/10.1002/rmb2.12085 |
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