Jae Yeon Hwang, Huafeng Wang, Gillian Clouser, Jong-Nam Oh, Sarah F Finnegan, Niels E Skakkebaek, Jean-Ju Chung
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引用次数: 0
摘要
鞭毛特异性 Ca 2+ 通道 CatSper 是一个多蛋白复合物,通过在空间和时间上控制精子的 Ca 2+ 信号传导,对成功受精至关重要。CATSPERβ、γ、δ和ε这四个单通道跨膜亚基的大细胞外结构域(ECD)在孔形成通道上形成了独特的冠层结构。然而,发育过程中顶盖组装的分子机制及其在成熟精子中的生理功能仍然未知。在这里,我们利用两种遗传小鼠模型和生物活性 CATSPERε 片段的生化分离,报告了 CATSPERε ECDs 对于组装 CatSper 冠层,进而组装整个通道复合物,以及调节 CatSper 功能以促进精子过度活化和受精至关重要。CATSPERε缺陷的雄性不育,因为它们的精子因缺乏整个通道而无法产生超活化运动。在睾丸生殖细胞中过表达具有截短ECD的CATSPERε的转基因小鼠中,截短的CATSPERε不能与原生的CatSper亚基相互作用并结合到复合物中,因此不能挽救Catspere-null雄性的精子超活化缺陷和不育症。这些发现让我们深入了解了CatSper复合体组装的潜在分子和发育机制,以及CatSper通道如何在生理环境下和通过治疗干预进行调节。
CATSPERϵ extracellular domains are essential for sperm calcium channel assembly and activity modulation.
The sperm flagellar-specific CatSper Ca2+ channel is a multiprotein complex critical for successful fertilization. The four ancillary subunits, CATSPERβ, γ, δ, and ε, form a unique canopy structure over the pore-forming channel. However, how the canopy is formed and what it does in the assembled channel complex remains unknown. Here, we report that extracellular domains (ECDs) of CATSPERε are essential for canopy and holo-complex assembly and modulate channel activity during sperm capacitation. CATSPERε-deficient males are sterile due to the absence of the entire channel and defective sperm hyperactivation. Expressing ECDs-truncated CATSPERε during spermatogenesis does not rescue the knockout because it fails to incorporate into the native complex. In contrast, addition of a CATSPERε ECD fragment during sperm capacitation significantly reduces channel activity. These findings provide insight into the underlying molecular and developmental mechanisms of CatSper assembly and how the channel can be modulated in physiological settings and by therapeutic intervention.