Kawai Y, Yoshikawa K, Hama T, Mayumi T
Faculty of Pharmaceutical Sciences, Kobe-Gakuin University, Kobe, Japan.
J Pharmacobiodyn. 1991 May;14(5):231-6. doi: 10.1248/bpb1978.14.231.
The epididymis has three major regions; the caput, corpus and cauda. Sperm were obtained from each region, and their binding ability to egg zona pellucida was assayed. In the case of intact sperm: cauda sperm bound in high number, corpus sperm bound at an intermediate level (an average of 30% of cauda sperm binding level), and caput sperm bound rarely (1% of cauda sperm binding level). In the case of sperm immobilized by pretreatment with LaCl3, when eggs and sperm were shaken in order to allow them to come into collision with each other, the caput and corpus sperm were able to bind to zona pellucida as well as the caudal sperm could. These results suggest that the difference in binding efficiency of the native caput and corpus sperm to bind to the zona pellucida was not due to a defect in a ligand molecule on the plasma membrane but rather to their lack of motility. When a sperm-egg binding assay was done in the presence of a binding inhibitor of caudal sperm, the binding of caudal sperm was significantly inhibited by fetuin or N-acetylgalactosamine, but the binding of caput and corpus sperm was only slightly inhibited by them. We prepared a plasma membrane fraction from each epididymal sperm, and solubilized it with sodium dodecyl sulfate (SDS). Each SDS-solubilizable fraction inhibited the binding of corresponding epididymal sperm to egg zona pellucida but didn't inhibit the binding of sperm from different regions of epididymis. These results suggested that a ligand molecule of caudal sperm was different from that of caput and corpus sperm.
头部、体部和尾部。从每个区域获取精子,并检测它们与卵透明带的结合能力。对于完整精子的情况:尾部精子大量结合,体部精子以中等水平结合(平均为尾部精子结合水平的30%),而头部精子很少结合(为尾部精子结合水平的1%)。对于用LaCl3预处理而固定的精子,当卵子和精子摇晃以使它们相互碰撞时,头部和体部精子能够与透明带结合,与尾部精子一样。这些结果表明,天然头部和体部精子与透明带结合效率的差异不是由于质膜上配体分子的缺陷,而是由于它们缺乏运动能力。当在尾部精子的结合抑制剂存在下进行精卵结合试验时,尾部精子的结合被胎球蛋白或N-乙酰半乳糖胺显著抑制,但头部和体部精子的结合仅被它们轻微抑制。我们从每个附睾精子制备了质膜部分,并用十二烷基硫酸钠(SDS)使其溶解。每个可被SDS溶解的部分抑制相应附睾精子与卵透明带的结合,但不抑制来自附睾不同区域精子的结合。这些结果表明,尾部精子的配体分子与头部和体部精子的不同。