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生理和合成类固醇对人类精子中钙通道CatSper的作用。

The action of physiological and synthetic steroids on the calcium channel CatSper in human sperm.

作者信息

Wehrli Lydia, Galdadas Ioannis, Voirol Lionel, Smieško Martin, Cambet Yves, Jaquet Vincent, Guerrier Stéphane, Gervasio Francesco Luigi, Nef Serge, Rahban Rita

机构信息

Department of Genetic Medicine and Development, University of Geneva, Geneva, Switzerland.

Swiss Centre for Applied Human Toxicology (SCAHT), Basel, Switzerland.

出版信息

Front Cell Dev Biol. 2023 Jul 20;11:1221578. doi: 10.3389/fcell.2023.1221578. eCollection 2023.

Abstract

The sperm-specific channel CatSper (cation channel of sperm) controls the intracellular Ca concentration ([Ca]) and plays an essential role in sperm function. It is mainly activated by the steroid progesterone (P4) but is also promiscuously activated by a wide range of synthetic and physiological compounds. These compounds include diverse steroids whose action on the channel is so far still controversial. To investigate the effect of these compounds on CatSper and sperm function, we developed a high-throughput screening (HTS) assay to measure changes in [Ca] in human sperm and screened 1,280 approved and off-patent drugs including 90 steroids from the Prestwick chemical library. More than half of the steroids tested (53%) induced an increase in [Ca] and reduced the P4-induced Ca influx in human sperm in a dose-dependent manner. Ten of the most potent steroids (activating and P4-inhibiting) were selected for a detailed analysis of their action on CatSper and their ability to act on sperm acrosome reaction (AR) and penetration in viscous media. We found that these steroids show an inhibitory effect on P4 but not on prostaglandin E1-induced CatSper activation, suggesting that they compete for the same binding site as P4. Pregnenolone, dydrogesterone, epiandrosterone, nandrolone, and dehydroepiandrosterone acetate (DHEA) were found to activate CatSper at physiologically relevant concentrations within the nanomolar range. Like P4, most tested steroids did not significantly affect the AR while stanozolol and estropipate slightly increased sperm penetration into viscous medium. Furthermore, using a hybrid approach integrating pharmacophore analysis and statistical modelling, we were able to screen for steroids that can activate the channel and define the physicochemical and structural properties required for a steroid to exhibit agonist activity against CatSper. Overall, our results indicate that not only physiological but also synthetic steroids can modulate the activity of CatSper with varying potency and if bound to CatSper prior to P4, could impair the timely CatSper activation necessary for proper fertilization to occur.

摘要

精子特异性通道CatSper(精子阳离子通道)控制细胞内钙离子浓度([Ca]),并在精子功能中发挥重要作用。它主要由甾体激素孕酮(P4)激活,但也会被多种合成化合物和生理化合物非特异性激活。这些化合物包括多种甾体,其对该通道的作用至今仍存在争议。为了研究这些化合物对CatSper和精子功能的影响,我们开发了一种高通量筛选(HTS)检测方法来测量人类精子中[Ca]的变化,并从Prestwick化学文库中筛选了1280种已获批和专利过期的药物,其中包括90种甾体。超过一半(53%)的受试甾体以剂量依赖的方式诱导人类精子中[Ca]升高,并减少P4诱导的钙离子内流。选择了十种最有效的甾体(激活和抑制P4的),详细分析它们对CatSper的作用以及它们对精子顶体反应(AR)和在粘性介质中穿透能力的影响。我们发现这些甾体对P4有抑制作用,但对前列腺素E1诱导的CatSper激活没有抑制作用,这表明它们与P4竞争相同的结合位点。孕烯醇酮、羟孕酮、表雄酮、诺龙和醋酸脱氢表雄酮(DHEA)在纳摩尔范围内的生理相关浓度下被发现可激活CatSper。与P4一样,大多数受试甾体对AR没有显著影响,而司坦唑醇和己烯雌酚略微增加了精子在粘性介质中的穿透能力。此外,通过整合药效团分析和统计建模的混合方法,我们能够筛选出可激活该通道的甾体,并确定甾体表现出针对CatSper的激动剂活性所需的物理化学和结构特性。总体而言,我们的结果表明,不仅生理甾体,合成甾体也可以不同效力调节CatSper的活性,如果在P4之前与CatSper结合,可能会损害受精正常发生所需的CatSper及时激活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ac/10397409/40497df3f459/fcell-11-1221578-g001.jpg

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