摘要：SummaryClassically, follicle-stimulating hormone receptor (FSHR)-driven cAMP-mediated signaling boosts human ovarian follicle growth and oocyte maturation. However, contradictingin vitrodata suggest a different view on physiological significance of FSHR-mediated cAMP signaling. We found that the G-protein-coupled estrogen receptor (GPER) heteromerizes with FSHR, reprogramming cAMP/death signals into proliferative stimuli fundamental for sustaining oocyte survival. In human granulosa cells, survival signals are missing at high FSHR:GPER ratio, which negatively impacts follicle maturation and strongly correlates with preferential Gαs protein/cAMP-pathway coupling and FSH responsiveness of patients undergoing controlled ovarian stimulation. In contrast, FSHR/GPER heteromers triggered anti-apoptotic/proliferative FSH signaling delivered via the Gβγ dimer, whereas impairment of heteromer formation or GPER knockdown enhanced the FSH-dependent cell death and steroidogenesis. Therefore, our findings indicate how oocyte maturation depends on the capability of GPER to shape FSHR selective signals, indicating hormone receptor heteromers may be a marker of cell proliferation.Graphical AbstractDisplay OmittedHighlights•G-protein-coupled estrogen receptor (GPER) interacts with FSH receptor (FSHR)•FSHR/GPER heteromers reprogram FSH-induced death signals to proliferative stimuli•Anti-apoptotic signaling of heteromers is via a GPER-Gαs inhibitory complex and Gβγ•Heteromer formation impacts follicle maturation and FSH responses of IVF patientsMolecular Biology; Female Reproductive Endocrinology; Endocrine Regulation
