» Articles » PMID: 31902805

Colocalization of GPR120 and Anterior Pituitary Hormone-producing Cells in Female Japanese Black Cattle

Overview
Journal J Reprod Dev
Date 2020 Jan 7
PMID 31902805
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

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.

Citing Articles

Ethanolamine plasmalogens derived from scallops stimulate both follicle-stimulating hormone and luteinizing hormone secretion by bovine gonadotrophs.

Kadokawa H, Kotaniguchi M, Mawatari S, Saito R, Fujino T, Kitamura S Sci Rep. 2022; 12(1):16789.

PMID: 36202862 PMC: 9537335. DOI: 10.1038/s41598-022-20794-4.


Age-associated changes in gene expression in the anterior pituitary glands of female Japanese black cattle.

Abdillah D, Kereilwe O, Mizukami Y, Watanabe K, Kadokawa H Mamm Genome. 2022; 33(4):606-618.

PMID: 35838775 DOI: 10.1007/s00335-022-09958-9.


Gpr120 mRNA expression in gonadotropes in the mouse pituitary gland is regulated by free fatty acids.

Deura C, Kimura Y, Nonoyama T, Moriyama R J Reprod Dev. 2020; 66(3):249-254.

PMID: 32115468 PMC: 7297631. DOI: 10.1262/jrd.2019-166.

References
1.
Pierce B, Stackpole C, Breen K, Clarke I, Karsch F, Rivalland E . Estradiol enables cortisol to act directly upon the pituitary to suppress pituitary responsiveness to GnRH in sheep. Neuroendocrinology. 2008; 89(1):86-97. DOI: 10.1159/000151543. View

2.
Minabe S, Uenoyama Y, Tsukamura H, Maeda K . Analysis of pulsatile and surge-like luteinizing hormone secretion with frequent blood sampling in female mice. J Reprod Dev. 2011; 57(5):660-4. DOI: 10.1262/jrd.11-078s. View

3.
Koyama H, Iwakura H, Dote K, Bando M, Hosoda H, Ariyasu H . Comprehensive Profiling of GPCR Expression in Ghrelin-Producing Cells. Endocrinology. 2015; 157(2):692-704. DOI: 10.1210/en.2015-1784. View

4.
Li S, Mbong E, John D, Terasaka T, Li D, Lawson M . Induction of Stress Signaling In Vitro and Suppression of Gonadotropin Secretion by Free Fatty Acids in Female Mouse Gonadotropes. Endocrinology. 2018; 159(2):1074-1087. PMC: 5793794. DOI: 10.1210/en.2017-00638. View

5.
Minabe S, Deura C, Ikegami K, Goto T, Sanbo M, Hirabayashi M . Pharmacological and Morphological Evidence of AMPK-Mediated Energy Sensing in the Lower Brain Stem Ependymocytes to Control Reproduction in Female Rodents. Endocrinology. 2015; 156(6):2278-87. PMC: 4430616. DOI: 10.1210/en.2014-2018. View