Mehlmann Lisa M
Department of Cell Biology, University of Connecticut Health Center, 263 Farmington Ave., Farmington, Connecticut 06032, USA.
Reproduction. 2005 Dec;130(6):791-9. doi: 10.1530/rep.1.00793.
Mammalian oocytes grow and undergo meiosis within ovarian follicles. Oocytes are arrested at the first meiotic prophase, held in meiotic arrest by the surrounding follicle cells until a surge of LH from the pituitary stimulates the immature oocyte to resume meiosis. Meiotic arrest depends on a high level of cAMP within the oocyte. This cAMP is generated by the oocyte, through the stimulation of the G(s) G-protein by the G-protein-coupled receptor, GPR3. Stimulation of meiotic maturation by LH occurs via its action on the surrounding somatic cells rather than on the oocyte itself. LH induces the expression of epidermal growth factor-like proteins in the mural granulosa cells that act on the cumulus cells to trigger oocyte maturation. The signaling pathway between the cumulus cells and the oocyte, however, remains unknown. This review focuses on recent studies highlighting the importance of the oocyte in producing cAMP to maintain arrest, and discusses possible targets at the level of the oocyte on which LH could act to stimulate meiotic resumption.
哺乳动物的卵母细胞在卵巢卵泡内生长并进行减数分裂。卵母细胞停滞于第一次减数分裂前期,被周围的卵泡细胞维持在减数分裂停滞状态,直到垂体分泌的促黄体生成素(LH)激增,刺激未成熟卵母细胞恢复减数分裂。减数分裂停滞取决于卵母细胞内高水平的环磷酸腺苷(cAMP)。这种cAMP由卵母细胞产生,通过G蛋白偶联受体GPR3对G(s) G蛋白的刺激作用而生成。LH对减数分裂成熟的刺激是通过其作用于周围的体细胞而非卵母细胞本身来实现的。LH诱导壁颗粒细胞中表皮生长因子样蛋白的表达,这些蛋白作用于卵丘细胞以触发卵母细胞成熟。然而,卵丘细胞与卵母细胞之间的信号通路仍不清楚。本综述重点关注近期研究,这些研究突出了卵母细胞产生cAMP以维持停滞状态的重要性,并讨论了LH可能作用于卵母细胞水平以刺激减数分裂恢复的潜在靶点。