Inaba Kazuo, Shiba Kogiku
Shimoda Marine Research Center, University of Tsukuba, 5-10-1 Shimoda, Shizuoka 415-0025, Japan.
Microscopy (Oxf). 2018 Jun 1;67(3):144-155. doi: 10.1093/jmicro/dfy021.
Cilia and flagella are cell machines that power hydrodynamic forces by fast beating. They are composed of bundles of 9 + 2 microtubules that associate with several protein structures including axonemal dyneins and their regulators. Spermatozoa are single cells with in most cases a single flagellum and are good cell models to study how flagellar movements are regulated and linked to cell behavior. In addition, the assessment of sperm motility is an important diagnostic tool for evaluating male fertility in human reproductive medicine, and in livestock and fisheries sciences. Microscopic analyses of the movements of spermatozoa and their flagellar waveforms and propagation have been carried out using high-speed cameras and stroboscopic illumination. Computer-assisted sperm analysis (CASA) now comprises an automated set of methods to evaluate sperm quality for fertility. Here, we summarize the microscopy systems used for evaluating sperm motility, including CASA, and introduce updates on the molecular mechanism of flagellar movement and regulation that are linked to motility parameters. Furthermore, we introduce recent techniques employed to measure key factors controlling sperm motility.
纤毛和鞭毛是通过快速摆动产生流体动力的细胞机器。它们由9 + 2微管束组成,这些微管束与包括轴丝动力蛋白及其调节因子在内的几种蛋白质结构相关联。精子是单细胞,在大多数情况下有一条鞭毛,是研究鞭毛运动如何被调节以及如何与细胞行为相联系的良好细胞模型。此外,评估精子活力是人类生殖医学、畜牧和渔业科学中评估男性生育能力的重要诊断工具。已经使用高速摄像机和频闪照明对精子的运动及其鞭毛波形和传播进行了显微镜分析。计算机辅助精子分析(CASA)现在包括一套自动评估生育能力精子质量的方法。在这里,我们总结了用于评估精子活力的显微镜系统,包括CASA,并介绍了与活力参数相关的鞭毛运动和调节分子机制的最新进展。此外,我们介绍了用于测量控制精子活力关键因素的最新技术。