Rehfeld Anders, Egeberg Palme Dorte Louise, Almstrup Kristian, Juul Anders, Skakkebaek Niels Erik
Department of Growth and Reproduction, Copenhagen University Hospital; International Center for Research and Research Training in Endocrine Disruption of Male Reproduction and Child Health (EDMaRC), University of Copenhagen;
Department of Growth and Reproduction, Copenhagen University Hospital; International Center for Research and Research Training in Endocrine Disruption of Male Reproduction and Child Health (EDMaRC), University of Copenhagen.
J Vis Exp. 2019 Mar 1(145). doi: 10.3791/59212.
Ca-signaling is essential to normal sperm cell function and male fertility. Similarly, the acrosome reaction is vital for the ability of a human sperm cell to penetrate the zona pellucida and fertilize the egg. It is therefore of great interest to test compounds (e.g., environmental chemicals or drug candidates) for their effect on Ca-signaling and acrosome reaction in human sperm either to examine the potential adverse effects on human sperm cell function or to investigate a possible role as a contraceptive. Here, two medium-throughput assays are described: 1) a fluorescence-based assay for assessment of effects on Ca-signaling in human sperm, and 2) an image cytometric assay for assessment of acrosome reaction in human sperm. These assays can be used to screen a large number of compounds for effects on Ca-signaling and acrosome reaction in human sperm. Furthermore, the assays can be used to generate highly specific dose-response curves of individual compounds, determine potential additivity/synergism for two or more compounds, and to study the pharmacological mode of action through competitive inhibition experiments with CatSper inhibitors.
钙信号对于正常精子细胞功能和男性生育能力至关重要。同样,顶体反应对于人类精子穿透透明带并使卵子受精的能力至关重要。因此,测试化合物(例如环境化学物质或候选药物)对人类精子中钙信号和顶体反应的影响非常有意义,这既可以检查对人类精子细胞功能的潜在不利影响,也可以研究其作为避孕药的可能作用。在此,描述了两种中通量测定法:1)基于荧光的测定法,用于评估对人类精子中钙信号的影响;2)图像细胞术测定法,用于评估人类精子中的顶体反应。这些测定法可用于筛选大量化合物对人类精子中钙信号和顶体反应的影响。此外,这些测定法可用于生成单个化合物的高度特异性剂量反应曲线,确定两种或更多种化合物的潜在加和性/协同性,并通过与CatSper抑制剂的竞争性抑制实验来研究药理作用模式。