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精子活力和趋化性的激活。

Activation of motility and chemotaxis in the spermatozoa.

作者信息

Yoshida Manabu, Yoshida Kaoru

机构信息

Misaki Marine Biological Station, School of Science The University of Tokyo Miura Kanagawa Japan.

Faculty of Biomedical Engineering Toin University of Yokohama Yokohama Kanagawa Japan.

出版信息

Reprod Med Biol. 2025 Mar 5;24(1):e12638. doi: 10.1002/rmb2.12638. eCollection 2025 Jan-Dec.

Abstract

BACKGROUND

Sperm motility and chemotaxis are important early steps in the interaction between sperm and oocytes during fertilization. Understanding these processes is essential for their basic biological and clinical applications. This review outlines advances in understanding the molecular mechanisms of sperm activation and chemotaxis over the past two decades.

METHODS

The review focuses on the molecular pathways of Ca signaling and the role of the CatSper channel involved in this signaling, and examines the comprehensive mechanisms that regulate sperm motility in aquatic invertebrates, fish, and mammals.

MAIN FINDINGS

Sperm are activated by environmental changes (e.g., pH and osmolality) and egg-derived factors. CatSper channels mediate Ca influx and regulate cell motility and chemotaxis. In addition to Ca, cAMP and membrane potential are also involved in the regulation of sperm motility. Alternative pathways exist in species lacking CatSper, highlighting the diversity of sperm activation mechanisms.

CONCLUSION

There has been significant progress in understanding sperm motility regulation mediated by Ca, notably with CatSper, but the molecular mechanisms of other factors remain unclear. Future research should focus on species lacking CatSper to uncover commonalities and diversity in sperm motility regulation using genome editing and transcriptomic analyses.

摘要

背景

精子活力和趋化性是受精过程中精子与卵母细胞相互作用的重要早期步骤。了解这些过程对其基础生物学和临床应用至关重要。本综述概述了过去二十年来在理解精子激活和趋化性分子机制方面取得的进展。

方法

本综述重点关注钙信号传导的分子途径以及参与该信号传导的CatSper通道的作用,并研究调节水生无脊椎动物、鱼类和哺乳动物精子活力的综合机制。

主要发现

精子被环境变化(如pH值和渗透压)和卵子衍生因子激活。CatSper通道介导钙内流并调节细胞活力和趋化性。除了钙,环磷酸腺苷(cAMP)和膜电位也参与精子活力的调节。在缺乏CatSper的物种中存在替代途径,突出了精子激活机制的多样性。

结论

在理解由钙介导的精子活力调节方面取得了重大进展,特别是与CatSper相关,但其他因素的分子机制仍不清楚。未来的研究应聚焦于缺乏CatSper的物种,利用基因组编辑和转录组分析揭示精子活力调节中的共性和多样性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c3a/11880775/a359cb5335a1/RMB2-24-e12638-g002.jpg

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