Mallett P J, Stock C E, Fraser L R
Int J Androl. 1985 Oct;8(5):357-64. doi: 10.1111/j.1365-2605.1985.tb00848.x.
Human sperm were incubated under capacitating conditions and, at selected points up to 24 h of incubation, motile cells were fixed and assessed with the electron microscope for the presence or absence of the acrosome. Two methods of sample preparation were compared. In the first, semen samples were washed, incubated and filtered through glass beads to select motile cells before fixation. In the second, motile sperm were allowed to swim up into medium; this produced greater than 95% motile cells which were then incubated and fixed as required. In both series of experiments a significant increase in acrosome loss with time was observed (P = 0.00013), although only 10.5% of cells had lost the acrosome after 24 h. It is concluded that overt acrosome loss occurs less frequently in human sperm than in those of commonly used laboratory animals.
将人类精子在获能条件下进行孵育,并在长达24小时的孵育过程中的选定时间点,对活动精子进行固定,然后用电子显微镜评估顶体的有无。比较了两种样品制备方法。第一种方法是,精液样本经洗涤、孵育后,通过玻璃珠过滤以选择活动精子,然后进行固定。第二种方法是,让活动精子游入培养基中;这样可产生超过95%的活动精子,然后根据需要进行孵育和固定。在这两个系列的实验中,均观察到顶体丢失随时间显著增加(P = 0.00013),尽管24小时后只有10.5%的细胞发生了顶体丢失。得出的结论是,人类精子中明显的顶体丢失比常用实验动物的精子中发生得更少。