Yeung W S, Ng V K, Lau E Y, Ho P C
Department of Obstetrics and Gynaecology, University of Hong Kong, Queen Mary Hospital.
Hum Reprod. 1994 Apr;9(4):656-60. doi: 10.1093/oxfordjournals.humrep.a138566.
The effects of the co-incubation of human oviductal cells with human spermatozoa on the general motility pattern and hyperactivation of spermatozoa in vitro were studied using computer-assisted sperm analysis. Co-incubation preserved all the sperm motility parameters, with the exception of the percentage of hyperactivation (HA), beat cross frequency (BCF), and the percentage of transitional hyperactivated (THA) spermatozoa, when compared with the initial motility pattern of the spermatozoa. The HA and THA decreased, and BCF increased after co-incubation for 3 h; these levels then remained stable up to 5 h. The control spermatozoa showed a continuous significant change after 5 h incubation. The oviductal cell-conditioned medium maintained all the motility parameters of spermatozoa even after 5 h incubation. These data suggested that human oviductal cells could maintain the motility of spermatozoa in vitro. Similar effects were also observed when conditioned medium was used to treat subnormal spermatozoa.
利用计算机辅助精子分析技术,研究了人输卵管细胞与人精子共同孵育对精子体外总体运动模式和超活化的影响。与精子的初始运动模式相比,共同孵育保留了所有精子运动参数,但超活化(HA)百分比、鞭打交叉频率(BCF)和过渡性超活化(THA)精子百分比除外。共同孵育3小时后,HA和THA降低,BCF增加;这些水平随后在长达5小时内保持稳定。对照精子在孵育5小时后显示出持续的显著变化。输卵管细胞条件培养基即使在孵育5小时后仍能维持精子的所有运动参数。这些数据表明,人输卵管细胞可以在体外维持精子的运动能力。当使用条件培养基处理弱精子症精子时,也观察到了类似的效果。