Institute of Reproductive Medicine, Medical School, Nantong University, Nantong, China.
Center for Reproductive Medicine, Affiliated Hospital of Nantong University, Nantong University, Nantong, China.
Front Endocrinol (Lausanne). 2024 Aug 16;15:1411000. doi: 10.3389/fendo.2024.1411000. eCollection 2024.
Calcium (Ca) is a second messenger for many signal pathways, and changes in intracellular Ca concentration ([Ca]i) are an important signaling mechanism in the oocyte maturation, activation, fertilization, function regulation of granulosa and cumulus cells and offspring development. Ca oscillations occur during oocyte maturation and fertilization, which are maintained by Ca stores and extracellular Ca ([Ca]e). Abnormalities in Ca signaling can affect the release of the first polar body, the first meiotic division, and chromosome and spindle morphology. Well-studied aspects of Ca signaling in the oocyte are oocyte activation and fertilization. Oocyte activation, driven by sperm-specific phospholipase PLCζ, is initiated by concerted intracellular patterns of Ca release, termed Ca oscillations. Ca oscillations persist for a long time during fertilization and are coordinately engaged by a variety of Ca channels, pumps, regulatory proteins and their partners. Calcium signaling also regulates granulosa and cumulus cells' function, which further affects oocyte maturation and fertilization outcome. Clinically, there are several physical and chemical options for treating fertilization failure through oocyte activation. Additionally, various exogenous compounds or drugs can cause ovarian dysfunction and female infertility by inducing abnormal Ca signaling or Ca dyshomeostasis in oocytes and granulosa cells. Therefore, the reproductive health risks caused by adverse stresses should arouse our attention. This review will systematically summarize the latest research progress on the aforementioned aspects and propose further research directions on calcium signaling in female reproduction.
钙(Ca)是许多信号通路的第二信使,细胞内钙浓度([Ca]i)的变化是卵母细胞成熟、激活、受精、颗粒细胞和卵丘细胞功能调节以及后代发育的重要信号机制。钙振荡发生在卵母细胞成熟和受精过程中,由钙储存和细胞外钙([Ca]e)维持。钙信号的异常会影响第一极体的释放、第一次减数分裂以及染色体和纺锤体形态。卵母细胞中钙信号研究较多的方面是卵母细胞激活和受精。卵母细胞激活是由精子特异性磷脂酶 PLCζ 驱动的,由协同的细胞内钙释放模式,即钙振荡启动。在受精过程中,钙振荡持续很长时间,并通过各种钙通道、泵、调节蛋白及其伴侣协调参与。钙信号还调节颗粒细胞和卵丘细胞的功能,进一步影响卵母细胞成熟和受精结局。临床上,有几种物理和化学方法可通过卵母细胞激活来治疗受精失败。此外,各种外源化合物或药物可通过诱导卵母细胞和颗粒细胞中异常的钙信号或钙稳态失调,导致卵巢功能障碍和女性不孕。因此,不良应激引起的生殖健康风险应引起我们的关注。本综述将系统总结上述方面的最新研究进展,并提出钙信号在女性生殖中的进一步研究方向。