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电信号在成熟精子中对通过电压感应磷酸酶调节磷酯酰肌醇的意义。

The significance of electrical signals in maturing spermatozoa for phosphoinositide regulation through voltage-sensing phosphatase.

机构信息

Graduate School of Medicine, Osaka University, Suita, Japan.

Department of Biochemical Pathophysiology/Lipid Biology, Medical Research Institute, Tokyo Medical and Dental University, Tokyo, Japan.

出版信息

Nat Commun. 2024 Aug 24;15(1):7289. doi: 10.1038/s41467-024-51755-2.

Abstract

Voltage-sensing phosphatase (VSP) exhibits voltage-dependent phosphatase activity toward phosphoinositides. VSP generates a specialized phosphoinositide environment in mammalian sperm flagellum. However, the voltage-sensing mechanism of VSP in spermatozoa is not yet characterized. Here, we found that VSP is activated during sperm maturation, indicating that electric signals in immature spermatozoa are essential. Using a heterologous expression system, we show the voltage-sensing property of mouse VSP (mVSP). The voltage-sensing threshold of mVSP is approximately -30 mV, which is sensitive enough to activate mVSP in immature spermatozoa. We also report several knock-in mice in which we manipulate the voltage-sensitivity or electrochemical coupling of mVSP. Notably, the V312R mutant, with a minor voltage-sensitivity change, exhibits abnormal sperm motility after, but not before, capacitation. Additionally, the V312R mutant shows a significant change in the acyl-chain profile of phosphoinositide. Our findings suggest that electrical signals during sperm maturation are crucial for establishing the optimal phosphoinositide environment in spermatozoa.

摘要

电压感应磷酸酶(VSP)对磷酸肌醇显示出电压依赖性磷酸酶活性。VSP 在哺乳动物精子鞭毛中产生特殊的磷酸肌醇环境。然而,精子中 VSP 的电压感应机制尚未被描述。在这里,我们发现 VSP 在精子成熟过程中被激活,这表明不成熟精子中的电信号是必不可少的。通过异源表达系统,我们展示了小鼠 VSP(mVSP)的电压感应特性。mVSP 的电压感应阈值约为-30 mV,足以激活不成熟的精子中的 mVSP。我们还报告了几种基因敲入小鼠,我们在其中操纵 mVSP 的电压敏感性或电化学偶联。值得注意的是,V312R 突变体,其电压敏感性变化较小,在获能后但不在获能前表现出异常的精子运动。此外,V312R 突变体在磷酸肌醇的酰基链谱中表现出显著变化。我们的发现表明,精子成熟过程中的电信号对于在精子中建立最佳的磷酸肌醇环境至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c853/11344830/fe39a5ee4bea/41467_2024_51755_Fig1_HTML.jpg

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