Acquisition of zona binding by ram spermatozoa during epididymal passage, as revealed by interaction with rat oocytes

S. Fournier-delpech, J. Courtens, C. Pisselet, B. Delaleu, M. Courot
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引用次数: 26

Abstract

To assess the ability of ram spermatozoa to bind to oocytes, spermatozoa (2.5–200 × 106/500μ1) taken from the rete testis, or from various regions of the epididymis (head, body, and tail) were mixed with cumulus-free heterologous oocytes obtained from immature superovulated rats. After incubation for 30–45 min in Parker 199 Hepes medium at 35°C, testicular spermatozoa were unable to bind to the zona at any of the concentrations used. However, spermatozoa from the middle body of the epididymus were able to bind to the zona and this binding reached a maximum in the distal body and in the tail of the epididymis. The spermatozoa were bound by their heads. Electron microscopy showed that the plasma membrane and the acrosome of the bound sperm remained intact, without any sign of an acrosome reaction.
通过与大鼠卵母细胞的相互作用揭示,公羊精子在附睾传代过程中获得带结合
为了评估公羊精子与卵母细胞的结合能力,将取自睾丸网或附睾各部位(头、体、尾)的精子(2.5 ~ 200 × 106/500μ1)与未成熟过排卵大鼠的无积丘异源卵母细胞混合。在35°C的Parker 199 Hepes培养基中孵育30-45分钟后,睾丸精子在任何浓度下都无法与带结合。然而,来自附睾中间体的精子能够与附睾带结合,这种结合在附睾远端体和附睾尾部达到最大。精子被它们的头束缚住了。电镜显示,结合精子的质膜和顶体保持完整,没有任何顶体反应的迹象。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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