| Literature DB >> 31087036 |
Jeremy R Egbert1, Paul G Fahey2, Jacob Reimer2, Corie M Owen1, Alexei V Evsikov3, Viacheslav O Nikolaev4, Oliver Griesbeck5, Russell S Ray2, Andreas S Tolias4,6, Laurinda A Jaffe1.
Abstract
In mammalian ovarian follicles, follicle stimulating hormone (FSH) and luteinizing hormone (LH) signal primarily through the G-protein Gs to elevate cAMP, but both of these hormones can also elevate Ca2+ under some conditions. Here, we investigate FSH- and LH-induced Ca2+ signaling in intact follicles of mice expressing genetically encoded Ca2+ sensors, Twitch-2B and GCaMP6s. At a physiological concentration (1 nM), FSH elevates Ca2+ within the granulosa cells of preantral and antral follicles. The Ca2+ rise begins several minutes after FSH application, peaks at ∼10 min, remains above baseline for another ∼10 min, and depends on extracellular Ca2+. However, suppression of the FSH-induced Ca2+ increase by reducing extracellular Ca2+ does not inhibit FSH-induced phosphorylation of MAP kinase, estradiol production, or the acquisition of LH responsiveness. Like FSH, LH also increases Ca2+, when applied to preovulatory follicles. At a physiological concentration (10 nM), LH elicits Ca2+ oscillations in a subset of cells in the outer mural granulosa layer. These oscillations continue for at least 6 h and depend on the activity of Gq family G-proteins. Suppression of the oscillations by Gq inhibition does not inhibit meiotic resumption, but does delay the time to 50% ovulation by about 3 h. In summary, both FSH and LH increase Ca2+ in the granulosa cells of intact follicles, but the functions of these Ca2+ rises are only starting to be identified.Entities:
Keywords: calcium; follicle; follicle-stimulating hormone; gonadotropins; granulosa cells; luteinizing hormone
Year: 2019 PMID: 31087036 PMCID: PMC7302518 DOI: 10.1093/biolre/ioz085
Source DB: PubMed Journal: Biol Reprod ISSN: 0006-3363 Impact factor: 4.285