Hormonal regulation of the ligand for c-kit in the rat ovary and its effects on spontaneous oocyte meiotic maturation
- 1 April 1996
- journal article
- Published by Wiley in Molecular Reproduction and Development
- Vol. 43 (4) , 458-469
- https://doi.org/10.1002/(sici)1098-2795(199604)43:4<458::aid-mrd8>3.0.co;2-o
Abstract
Kit ligand (KL, c‐kit ligand) mRNA was detected in the ovaries of 26‐day‐old prepubertal rats using in situ hybridization. In antral follicles there was a gradient in the intensity of the hybridization signal across the layers of granulosa cells, with greatest intensity observed in the cumulus granulosa cells enclosing the oocyte, and less signal occurring in the granulosa cells furthest from the oocyte. In age‐matched rats 40 hr after injection of pregnant mare serum gonadotropin (PMSG), the pattern of distribution of KL resembled that in the untreated ovaries, although the intensity of the hybridization signal was greater in the PMSG‐primed ovaries. This morphological observation was confirmed using Northern blot analysis, which indicated that granulosa cells of PMSG‐treated rats had 3.5‐fold greater abundance of KL mRNA compared to untreated rats. The abundance of KL mRNA further increased to 7‐fold over control levels at 6 hr after PMSG‐primed rats were treated with human chorionic gonadotropin (hCG). By contrast, treatment of rats with diethylstilbestrol to stimulate follicular growth did not cause any change in the abundance of KL transcripts. To investigate a potential role for KL in oocyte meiotic maturation, fully grown oocytes were cultured for 24 hr with or without KL (50 or 500 ng/ml). The presence of KL resulted in a significant, albeit transient, delay in the progression of spontaneous meiotic maturation, using the indices of germinal vesicle breakdown and polar body formation. The inhibitory effects of KL were specifically blocked by ACK2, an antibody to the extracellular domain of the c‐kit receptor. These results indicate that KL is produced in rat granulosa cells at particularly high levels in the cells closest to the oocyte and that this production may be regulated directly by gonadotropic hormones. Furthermore, KL inhibits the progression of meiosis in cultured oocytes, which suggests a possible role in the maintenance of meiotic arrest that occurs throughout oocyte growth. © 1996 Wiley Liss Inc.Keywords
This publication has 68 references indexed in Scilit:
- Expression of the mRNA for the ligand of C-kit in mouse sertoli cellsBiochemical and Biophysical Research Communications, 1991
- Developmental pattern of the secretion of cumulus expansion-enabling factor by mouse oocytes and the role of oocytes in promoting granulosa cell differentiationDevelopmental Biology, 1990
- Mouse oocytes regulate hyaluronic acid synthesis and mucification by FSH-stimulated cumulus cellsDevelopmental Biology, 1990
- FSH-induced expansion of the mouse cumulus oophorus in vitro is dependent upon a specific factor(s) secreted by the oocyteDevelopmental Biology, 1990
- Infertility due to growth arrest of ovarian follicles in miceDevelopmental Biology, 1988
- Aminoalkylsilane-treated glass slides as support forin situ hybridization of keratin cDNAs to frozen tissue sections under varying fixation and pretreatment conditionsJournal of Molecular Histology, 1986
- Regulation of oocyte maturation in the mouse: Possible roles of intercellular communication, cAMP, and testosteroneDevelopmental Biology, 1983
- The role of oocyte maturation inhibitor in follicular regulation of oocyte maturationReproduction, 1982
- Mouse oocyte development in vitro with various culture systemsDevelopmental Biology, 1977
- Hamster oocyte maturation : Inhibition by follicular componentsLife Sciences, 1976