Gonadotropin and steroid control of granulosa cell proliferation during the periovulatory interval in rhesus monkeys

C. L. Chaffin, K. M. Schwinof, R. L. Stouffer

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    50 Scopus citations


    Progesterone produced in response to the midcycle gonadotropin surge is essential for ovulation and luteinization of the primate follicle. Because cell-cycle arrest is associated with the initiation of luteinization, this study was designed to determine the dynamics and regulation of granulosa cell proliferation by gonadotropin and progesterone during the periovulatory interval in the primate follicle. Granulosa cells or ovaries were obtained from macaques undergoing controlled ovarian stimulation either before (0 h) or as long as 36 h following the administration of an ovulatory hCG bolus with or without a 3β-hydroxysteroid dehydrogenase inhibitor with or without a nonmetabolizable progestin. The percentage of cells staining positive for Ki-67, a nuclear marker for cell proliferation, decreased (P < 0.05) within 12 h of hCG administration in a steroid-independent manner. Levels of cyclin D2 and E mRNA did not decline during the periovulatory interval; however, cyclin B1 mRNA was reduced significantly by 12 h. Steroid depletion increased (P < 0.05) cyclin B1 mRNA at both 12 and 36 h post-hCG and was reversible by progestin replacement at 36 h. The cyclin-dependent kinase inhibitor p21Cip1 was transiently increased 12 h post-hCG, whereas p27Kip1 mRNA levels increased at 36 h in a steroid-independent fashion. These data suggest that a gonadotropin bolus inhibits mitosis in granulosa cells early (12 h) in the periovulatory interval, whereas progesterone may play a later, antiproliferative role in luteinized cells of primates.

    Original languageEnglish (US)
    Pages (from-to)755-762
    Number of pages8
    JournalBiology of reproduction
    Issue number3
    StatePublished - 2001


    • Corpus luteum
    • Granulosa cells
    • Human chorionic gonadotropin
    • Ovulation
    • Progesterone

    ASJC Scopus subject areas

    • Reproductive Medicine
    • Cell Biology


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