Department of Regulatory Physiology, Dokkyo Medical University, Mibu-machi, Tochigi 321-0293, Japan.
Department of Biomedical Technology, Faculty of Biomedical Engineering, Toin University of Yokohama, Yokohama 225-8502, Japan.
Mol Hum Reprod. 2017 Dec 1;23(12):817-826. doi: 10.1093/molehr/gax055.
What is the role of metachronal and synchronous sliding in sperm flagellar motility?
Both metachronal and oscillatory synchronous sliding are essential for sperm flagellar motility, while the change in mode of synchronous sliding between the non-oscillatory synchronous sliding of a specific pair of the doublet microtubules and the oscillatory synchronous sliding between most pairs of doublet microtubules modulates the sperm flagellar motility.
Metachronal and synchronous sliding of doublet microtubules are involved in sperm flagellar motility and regulation of these sliding movements controls flagellar bend formation.
STUDY DESIGN, SIZE, DURATION: To study the regulatory mechanisms of metachronal and synchronous sliding in flagellar movement of golden hamster spermatozoa, changes in these sliding movements during hyperactivation were examined by measuring the angle of the tangent to the flagellar shaft with reference to the central axis of the sperm head (the shear angle) along the flagellum. Golden hamster spermatozoa were obtained from the caudal epididymis of five sexually mature golden hamsters. Results from three experiments were averaged. The number of spermatozoa analyzed is 15 activated sperm, 22 hyperactivated sperm and 20 acrosome-reacted sperm.
PARTICIPANTS/MATERIALS, SETTING, METHODS: For detailed field-by-field analysis, an individual flagellar image was tracked automatically using the Autotrace module of image analysis software. The coordinate values of the flagellar shaft were used to calculate the shear angle, which is proportional to the amount of microtubule sliding at any given position along the flagellum. The maximum shear angles of metachronal and synchronous sliding were obtained from the mean shear angles between the maximum shear angles of pro-hook bends and the absolute values of the minimum shear angles of anti-hook bends, which represent the amplitude of a set of successive shear angle curves, with 3-12 shear curves covering one beat cycle of sperm flagellar movement. Asymmetry of flagellar waves was expressed by the mean shear angle between the maximum shear angle of pro-hook bends and the minimum shear angle of anti-hook bends at 100 μm from the head-midpiece junction.
The asymmetrical flagellar movements observed in the activated (non-hyperactivated) and hyperactivated spermatozoa were characterized by the non-oscillatory synchronous sliding of a specific pair of the doublets; the large asymmetrical flagellar movement in the hyperactivated spermatozoa was generated by the large non-oscillatory synchronous sliding. Both the metachronal and synchronous sliding increased during the hyperactivation; however, the large symmetrical flagellar movement of the acrosome-reacted spermatozoa was characterized by the oscillatory synchronous sliding between most pairs of doublets. These results demonstrated that the metachronal and synchronous sliding are involved in generation and modulation of sperm flagellar motility; however, two types of synchronous sliding, non-oscillatory and oscillatory sliding, modulate the sperm flagellar motility by enhancing the sliding of a specific pair of the doublets or the sliding between most pairs of the doublets.
None.
LIMITATIONS, REASONS FOR CAUTION: This is an indirect study of the metachronal and synchronous sliding of doublet microtubules. Studies based on the direct observation of behavior of dynein are needed to clarify the sliding microtubule theory of flagellar movement of spermatozoa.
Both the metachronal and oscillatory synchronous sliding of doublet microtubule generate and modulate sperm flagellar motility, while the change in mode of synchronous sliding between the non-oscillatory synchronous sliding and oscillatory synchronous sliding modulates the sperm flagellar motility. The coordination between these sliding leads to various types of flagellar and ciliary motility, including the asymmetrical beating in flagellar and ciliary movement and planar or helical beating in sea urchin spermatozoa. Moreover, the finding that the metachronal sliding and two types of synchronous sliding generate and modulate the flagellar motility will open a new avenue for quantitative analysis of flagellar and ciliary motility.
STUDY FUNDING AND COMPETING INTEREST(S): The authors have no conflict of interest and no funding to declare.
同步滑动和协同滑动在精子鞭毛运动中的作用是什么?
同步滑动和协同滑动对精子鞭毛运动都是必不可少的,而在非振荡同步滑动和大多数对双联体微管之间的振荡同步滑动之间的同步滑动模式的变化调节精子鞭毛运动。
双联体微管的协同滑动和协同滑动参与了精子鞭毛运动,并且这些滑动运动的调节控制着鞭毛弯曲的形成。
研究设计、大小、持续时间:为了研究金黄仓鼠精子鞭毛运动中同步滑动的调节机制,通过测量相对于精子头部中心轴(剪切角)的鞭毛轴切线的角度来检查超激活过程中这些滑动运动的变化。从五只性成熟金黄仓鼠的尾部附睾中获得金黄仓鼠精子。对三个实验的结果进行平均处理。分析的精子数量为 15 个激活精子,22 个超激活精子和 20 个顶体反应精子。
参与者/材料、设置、方法:对于详细的场域分析,使用图像分析软件的 Autotrace 模块自动跟踪单个鞭毛图像。鞭毛轴的坐标值用于计算剪切角,剪切角与给定位置的微管滑动量成正比。通过从最大钩弯的平均剪切角和反钩弯绝对值的最小剪切角之间获得最大的同步滑动和协同滑动的剪切角,这代表一组连续剪切角曲线的幅度,其中 3-12 个剪切曲线覆盖一个精子鞭毛运动的节拍周期。通过从头部中片连接处以 100μm 处的最大钩弯的平均剪切角和最小反钩弯的剪切角之间的平均值来表示鞭毛波的不对称性。
在激活(非超激活)和超激活精子中观察到的不对称鞭毛运动的特征是特定对双联体的非振荡同步滑动;超激活精子中较大的不对称鞭毛运动是由较大的非振荡同步滑动产生的。在超激活过程中,协同滑动和协同滑动都增加了;然而,顶体反应精子的大对称鞭毛运动的特征是大多数双联体之间的振荡同步滑动。这些结果表明,协同滑动和同步滑动参与了精子鞭毛运动的产生和调节;然而,两种类型的同步滑动,非振荡和振荡滑动,通过增强特定对双联体的滑动或大多数对双联体之间的滑动来调节精子鞭毛运动。
无。
限制、谨慎的原因:这是对双联体微管的协同滑动的间接研究。需要基于对动力蛋白行为的直接观察的研究来阐明精子鞭毛运动的微管滑动理论。
双联体微管的协同滑动和振荡同步滑动都产生和调节精子鞭毛运动,而在非振荡同步滑动和振荡同步滑动之间的同步滑动模式的变化调节精子鞭毛运动。这些滑动之间的协调导致各种类型的鞭毛和纤毛运动,包括鞭毛和纤毛运动中的不对称拍打以及海胆精子中的平面或螺旋拍打。此外,发现协同滑动和两种类型的同步滑动产生和调节鞭毛运动将为鞭毛和纤毛运动的定量分析开辟新的途径。
作者没有利益冲突,也没有资金申报。