Caballero Ignacio, Vázquez Juan M, García Eva M, Roca Jordi, Martínez Emilio A, Calvete Juan J, Sanz Libia, Ekwall Hans, Rodríguez-Martínez Heriberto
Departamento de Medicina y Cirugía Animal, Facultad de Veterinaria, Universidad de Murcia, Murcia, Spain.
J Androl. 2006 Nov-Dec;27(6):766-73. doi: 10.2164/jandrol.106.000539. Epub 2006 Jun 28.
PSP-I/PSP-II heterodimer is a major protein of boar seminal plasma which is able to preserve, in vitro, the viability, motility, and mitochondrial activity of highly extended boar spermatozoa for at least 5 hours. However, little is known about the binding pattern of the heterodimer to the sperm plasma membrane and its eventual relation with the maintenance of the sperm functionality. The present study investigated the effect of exposing highly extended boar spermatozoa (1 million/mL) to 1.5 mg/mL of PSP-I/PSP-II for 0.5, 5, and 10 hours at 38 degrees C on sperm characteristics and the changes in PSP-I/PSP-II localization as a result of both the addition of PSP-I/PSP-II to the extender and the incubation time. Exposure of the spermatozoa to PSP-I/PSP-II preserved sperm viability, motility, and mitochondrial activity when compared to nonexposed spermatozoa. This protective effect lasted for 10 hours (P < .05). After immunolabeling of highly extended semen with rabbit monospecific polyclonal antibody against PSP-I/PSP-II, the percentage of immunopositive spermatozoa declines over time from 71% (0.5 hours) to 49% (10 hours). However, more than 80% of spermatozoa remained labeled during the 10-hour incubation period if PSP-I/PSP-II was added. Scanning electron microscopy revealed 4 different binding patterns. The heterodimer was mainly localized to the acrosomal area, being redistributed to the postacrosomal area or lost during in vitro incubation. In conclusion, the protective effect of the heterodimer appears to be related to its adhesion to the acrosomal area, and the loss of this protective effect coincides with a stepwise redistribution of PSP-I/PSP-II during incubation.
PSP-I/PSP-II异二聚体是公猪精浆中的一种主要蛋白质,它能够在体外使高度稀释的公猪精子的活力、运动能力和线粒体活性至少保持5小时。然而,关于该异二聚体与精子质膜的结合模式及其与精子功能维持的最终关系,人们所知甚少。本研究调查了在38℃下,将高度稀释的公猪精子(100万/mL)暴露于1.5 mg/mL的PSP-I/PSP-II中0.5、5和10小时对精子特性的影响,以及由于向稀释液中添加PSP-I/PSP-II和孵育时间导致的PSP-I/PSP-II定位变化。与未暴露的精子相比,精子暴露于PSP-I/PSP-II后,其活力、运动能力和线粒体活性得以保持。这种保护作用持续了10小时(P < 0.05)。用抗PSP-I/PSP-II的兔单特异性多克隆抗体对高度稀释的精液进行免疫标记后,免疫阳性精子的百分比随时间从71%(0.5小时)下降到49%(10小时)。然而,如果添加了PSP-I/PSP-II,超过80%的精子在10小时的孵育期内仍有标记。扫描电子显微镜揭示了4种不同的结合模式。该异二聚体主要定位于顶体区域,在体外孵育过程中重新分布到顶体后区域或消失。总之,异二聚体的保护作用似乎与其在顶体区域的黏附有关,而这种保护作用的丧失与孵育过程中PSP-I/PSP-II的逐步重新分布相一致。