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Colocalization of GPR120 and anterior pituitary hormone-producing cells in female Japanese Black cattle
Negative energy balance in domestic animals suppresses their reproductive function. These animals commonly use long-chain fatty acids (LCFAs) from adipocytes as an energy source under states of malnutrition. The G-protein coupled receptor, GPR120, is a specific receptor for LCFAs, but its role in re...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Society for Reproduction and Development
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7175391/ https://www.ncbi.nlm.nih.gov/pubmed/31902805 http://dx.doi.org/10.1262/jrd.2019-111 |
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author | NAKAMURA, Sho NODA, Kohei MIWA, Masafumi MINABE, Shiori HAGIWARA, Teruki HIRASAWA, Akira MATSUYAMA, Shuichi MORIYAMA, Ryutaro |
author_facet | NAKAMURA, Sho NODA, Kohei MIWA, Masafumi MINABE, Shiori HAGIWARA, Teruki HIRASAWA, Akira MATSUYAMA, Shuichi MORIYAMA, Ryutaro |
author_sort | NAKAMURA, Sho |
collection | PubMed |
description | Negative energy balance in domestic animals suppresses their reproductive function. These animals commonly use long-chain fatty acids (LCFAs) from adipocytes as an energy source under states of malnutrition. The G-protein coupled receptor, GPR120, is a specific receptor for LCFAs, but its role in reproductive function remains unknown in domestic animals. The purpose of this study was to examine whether GPR120 is involved in the reproductive system of cattle. GPR120 mRNA expression was evaluated in brain, pituitary, and ovarian tissue samples by RT-PCR. GPR120 gene expression was detected with high intensity only in the anterior pituitary sample, and GPR120-immunoreactive cells were found in the anterior pituitary gland. Double immunohistochemistry of GPR120 in the anterior pituitary hormone-producing cells, such as gonadotropes, thyrotropes, lactotropes, somatotropes, and corticotropes, was performed to clarify the distribution of GPR120 in the anterior pituitary gland of ovariectomized heifers. Luteinizing hormone β subunit (LHβ)- and follicle-stimulating hormone β subunit (FSHβ)-immunoreactive cells demonstrated GPR120 immunoreactivity at 80.7% and 85.9%, respectively. Thyrotropes, lactotropes, somatotropes, and corticotropes coexpressed GPR120 at 21.1%, 5.4%, 13.6%, and 14.5%, respectively. In conclusion, the present study suggests that GPR120 in the anterior pituitary gland might mediate LCFA signaling to regulate gonadotrope functions, such as hormone secretion or production, in cattle. |
format | Online Article Text |
id | pubmed-7175391 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Society for Reproduction and Development |
record_format | MEDLINE/PubMed |
spelling | pubmed-71753912020-04-27 Colocalization of GPR120 and anterior pituitary hormone-producing cells in female Japanese Black cattle NAKAMURA, Sho NODA, Kohei MIWA, Masafumi MINABE, Shiori HAGIWARA, Teruki HIRASAWA, Akira MATSUYAMA, Shuichi MORIYAMA, Ryutaro J Reprod Dev Original Article Negative energy balance in domestic animals suppresses their reproductive function. These animals commonly use long-chain fatty acids (LCFAs) from adipocytes as an energy source under states of malnutrition. The G-protein coupled receptor, GPR120, is a specific receptor for LCFAs, but its role in reproductive function remains unknown in domestic animals. The purpose of this study was to examine whether GPR120 is involved in the reproductive system of cattle. GPR120 mRNA expression was evaluated in brain, pituitary, and ovarian tissue samples by RT-PCR. GPR120 gene expression was detected with high intensity only in the anterior pituitary sample, and GPR120-immunoreactive cells were found in the anterior pituitary gland. Double immunohistochemistry of GPR120 in the anterior pituitary hormone-producing cells, such as gonadotropes, thyrotropes, lactotropes, somatotropes, and corticotropes, was performed to clarify the distribution of GPR120 in the anterior pituitary gland of ovariectomized heifers. Luteinizing hormone β subunit (LHβ)- and follicle-stimulating hormone β subunit (FSHβ)-immunoreactive cells demonstrated GPR120 immunoreactivity at 80.7% and 85.9%, respectively. Thyrotropes, lactotropes, somatotropes, and corticotropes coexpressed GPR120 at 21.1%, 5.4%, 13.6%, and 14.5%, respectively. In conclusion, the present study suggests that GPR120 in the anterior pituitary gland might mediate LCFA signaling to regulate gonadotrope functions, such as hormone secretion or production, in cattle. The Society for Reproduction and Development 2019-12-27 2020-04 /pmc/articles/PMC7175391/ /pubmed/31902805 http://dx.doi.org/10.1262/jrd.2019-111 Text en ©2020 Society for Reproduction and Development This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: https://creativecommons.org/licenses/by-nc-nd/4.0/) |
spellingShingle | Original Article NAKAMURA, Sho NODA, Kohei MIWA, Masafumi MINABE, Shiori HAGIWARA, Teruki HIRASAWA, Akira MATSUYAMA, Shuichi MORIYAMA, Ryutaro Colocalization of GPR120 and anterior pituitary hormone-producing cells in female Japanese Black cattle |
title | Colocalization of GPR120 and anterior pituitary hormone-producing cells in female Japanese Black cattle |
title_full | Colocalization of GPR120 and anterior pituitary hormone-producing cells in female Japanese Black cattle |
title_fullStr | Colocalization of GPR120 and anterior pituitary hormone-producing cells in female Japanese Black cattle |
title_full_unstemmed | Colocalization of GPR120 and anterior pituitary hormone-producing cells in female Japanese Black cattle |
title_short | Colocalization of GPR120 and anterior pituitary hormone-producing cells in female Japanese Black cattle |
title_sort | colocalization of gpr120 and anterior pituitary hormone-producing cells in female japanese black cattle |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7175391/ https://www.ncbi.nlm.nih.gov/pubmed/31902805 http://dx.doi.org/10.1262/jrd.2019-111 |
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