Lacham O, Trounson A
Centre for Early Human Development, Monash University, Monash Medical Centre, Victoria, Australia.
Mol Reprod Dev. 1991 May;29(1):85-93. doi: 10.1002/mrd.1080290113.
Mouse spermatozoa were obtained from the testis and caput, corpus, and cauda epididymis incubated for 2 h in capacitation medium and a single spermatozoon from the capacitated samples microinjected into the pervitelline space of mature mouse oocytes. Spermatozoa from the testis were unable to fertilize oocytes and few spermatozoa from the caput were capable of fertilization (0-7% depending on the method of preparation). Similar fertilization rates (30-45%) were obtained with spermatozoa with forward progressive motility from the proximal and distal corpus and the cauda epididymis, but those that were vibratory or with local circular motility had significantly reduced fertilizing capacity (6-10%). The capacity of spermatozoa from the different regions of the testis and epididymis to bind to zona-free oocytes followed the same pattern as fertilization rate after microinjection. There was a progressive increase in acrosome reactions after 2 h incubation in capacitation medium in samples obtained from the testis to the cauda epididymis. Maturation of the capacity to bind to the perivitelline membrane and to develop forward progressive motility, rather than the capacity to acrosome react, appears to govern the fertilization of oocytes in which the zona has been bypassed by microinjection. These characteristics are obtained in the proximal segment of the corpus. However, there was evidence that the embryo developmental capacity of oocytes fertilized by spermatozoa from the higher segments of the epididymis is reduced, particularly in oocytes fertilized by caput spermatozoa. These observations suggest that sperm microinjection may have only a limited benefit for improving fertilization rates for men with high epididymal obstructive azoospermia.
从睾丸以及附睾头、附睾体和附睾尾获取小鼠精子,将其在获能培养基中孵育2小时,然后从获能样本中挑选单个精子显微注射到成熟小鼠卵母细胞的卵周隙中。来自睾丸的精子无法使卵母细胞受精,来自附睾头的精子只有少数能够受精(取决于制备方法,受精率为0 - 7%)。来自附睾体近端和远端以及附睾尾的具有向前运动能力的精子,其受精率相似(30 - 45%),但那些呈振动或局部圆周运动的精子受精能力显著降低(6 - 10%)。来自睾丸和附睾不同区域的精子与去透明带卵母细胞结合的能力,与显微注射后的受精率呈现相同模式。在获能培养基中孵育2小时后,从睾丸到附睾尾获取的样本中顶体反应逐渐增加。与顶体反应能力相比,与卵周膜结合以及产生向前运动能力的成熟似乎决定了通过显微注射绕过透明带的卵母细胞的受精情况。这些特性在附睾体的近端部分获得。然而,有证据表明,由附睾较高部位的精子使卵母细胞受精后,胚胎的发育能力会降低,尤其是由附睾头精子使卵母细胞受精的情况。这些观察结果表明,对于患有高位附睾梗阻性无精子症的男性,精子显微注射在提高受精率方面可能只有有限的益处。