Saling P M
Biol Reprod. 1982 Apr;26(3):429-36. doi: 10.1095/biolreprod26.3.429.
Mouse spermatozoa recovered from the caput, corpus, or cauda epididymidis were examined for their ability to bind the vitro to zonae pellucidae. Since spermatozoa from the caput epididymidis do not display progressive motility as compared with more mature spermatozoa, direct comparison of the different sperm populations may not measure zona binding ability validly. To equalize the motile properties of the spermatozoa, a method was developed to immobilize vigorously motile corpus and cauda spermatozoa. Reversible immobilization was achieved by incubation in 25 microM La3+ which resulted in a twitching, nonprogressive type of motility. La3+ incubation did not appear to affect the spermatozoa adversely, since vigorous motility (equivalent to the controls) of corpus and cauda sperm was displayed upon subsequent incubation in standard La3+-free culture medium. Moreover, cauda spermatozoa preincubated for 90 min in La3+ displayed levels of fertilization in vitro equivalent to their control counterparts. Using this La3+-immobilization technique, the zona binding ability of the different sperm population could be assayed. Gamete collision was insured under these conditions by shaking the gamete-containing dishes at 100 cycles/min. Regardless of the extent of sperm motility, a similar zona-binding pattern emerged: cauda sperm bound in high numbers, corpus sperm bound at some intermediate level (an average of 24% of cauda binding level), and caput sperm bound rarely (2% of cauda binding level). Thus it appears that, for mouse spermatozoa, the onset of fertility during epididymal transit parallels the ability to bind to zonae pellucidae. Unlike the interaction between spermatozoa and zonae, La3+ was unable to support sperm binding in to egg plasma membrane, supporting the view that mouse sperm may have different sites for interaction with the zonae pellucida and the egg plasma membrane.
对从附睾头、附睾体或附睾尾回收的小鼠精子进行体外结合透明带能力的检测。由于附睾头精子与更成熟的精子相比不表现出渐进性运动,不同精子群体的直接比较可能无法有效衡量透明带结合能力。为了使精子的运动特性均等,开发了一种方法来固定活力旺盛的附睾体和附睾尾精子。通过在25微摩尔/升的La3+中孵育实现可逆固定,这导致一种抽搐的、非渐进性的运动类型。La3+孵育似乎没有对精子产生不利影响,因为在随后于不含La3+的标准培养基中孵育时,附睾体和附睾尾精子表现出旺盛的运动能力(与对照组相当)。此外,在La3+中预孵育90分钟的附睾尾精子在体外的受精水平与其对照相当。使用这种La3+固定技术,可以检测不同精子群体的透明带结合能力。在这些条件下,通过以每分钟100次循环摇动含有配子的培养皿来确保配子碰撞。无论精子运动程度如何,都出现了类似的透明带结合模式:附睾尾精子大量结合,附睾体精子在中间水平结合(平均为附睾尾结合水平的24%),附睾头精子很少结合(为附睾尾结合水平的2%)。因此,对于小鼠精子来说,附睾转运过程中生育能力的开始与结合透明带的能力平行。与精子和透明带之间的相互作用不同,La3+不能支持精子与卵质膜结合,这支持了小鼠精子可能有不同位点与透明带和卵质膜相互作用的观点。