期刊
THERIOGENOLOGY
卷 96, 期 -, 页码 126-135出版社
ELSEVIER SCIENCE INC
DOI: 10.1016/j.theriogenology.2017.04.014
关键词
Apelin; APJ; Steroidogenesis; Proliferation; Ovarian follicle
资金
- Jagiellonian University in Krakow [DSC/MND/WBiNoZ/IZ/5/2014]
- Ministry of Science and Higher Education
Apelin was thought to be an adipocyte-specific hormone, but recent studies indicate a link between apelin and female reproductive function. Using real-time PCR, immunoblotting, immunohistochemistry and ELISA, we demonstrated expression of apelin and its receptor (APJ) in ovarian follicles of different sizes from mature pigs. Apelin concentration in the follicular fluid, and expression of both apelin and APJ, increased with follicular growth; greatest values were found in large follicles. immunohistochemistry revealed the positive staining for apelin and APJ in membranes of granulosa, than theca cells. Furthermore, we observed strong expression of apelin in oocytes and APJ in the zona pellucida. The effect of apelin (0.02, 0.2, 2 and 20 ng/ml) on basal and IGF1- and FSH-induced steroid hormone (progesterone [P41, and estradiol [E2]) secretion, steroidogenic enzyme (3 beta HSD and CYP19A1) expression and cell proliferation (Alamar blue) was determined. Apelin was found to increase basal steroid secretion, but decrease IGFI- and FSH-induced steroid secretion, and 3 beta HSD and CYP19 expression. Apelin also increased cell proliferation and the phosphorylation level of 5'-monophosphate-activated protein kinase (AMPK), phosphatidyl inositol 3' kinase/Akt (Akt) and extracellular signal-regulated kinases (ERK1 /2). AMPKrz was involved in the action of apelin in P4 production, and MAPK/ERK and Akt/PI3 mediated the proliferative effect of apelin. However, these effects on steroid secretion and cell proliferation were abolished when cultured in the presence of ML221, an APJ antagonist. In conclusion, apelin appears to regulate ovarian follicular functions such as steroidogenesis and proliferation via APJ activation and different signaling pathways. (C) 2017 Elsevier Inc. All rights reserved.
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