Isahakia M A
Institute of Primate Research, National Museums of Kenya, Nairobi.
Biol Reprod. 1988 Nov;39(4):889-99. doi: 10.1095/biolreprod39.4.889.
Sperm antigens that appear during spermatogenesis in the baboon were identified by using three monoclonal antibodies generated in culture from mice immunized with baboon caudal epididymal spermatozoa. Antibodies BSA1 and BSA2 recognize trypsin-sensitive 84,000 and 45,000 dalton determinants that are restricted to the tail and anterior acrosomal regions of the sperm, respectively, as determined by Western blot and immunofluorescence techniques. The tail antigen absent in 2- and 3-yr-old baboon testes first appears in spermatid cells at about 4 yr of age. In contrast, the acrosomal antigen recognized by BSA2 is present in 3-yr-old primitive testicular germ cells. In the mature testis, the 45,000 molecular weight determinant is predominantly localized in the nucleus of late pachytene spermatocytes and round spermatid cells as observed via the avidinbiotin immunoperoxidase method. Antibody BSA3 reacted only with sailidase-treated sections of adult testis. This trypsin-resistant determinant, not expressed on testicular sperm, is recognized by antibody BSA3 only on epididymal sperm, thus indicating a post-testicular sperm modification.
通过使用三种由用狒狒附睾尾精子免疫的小鼠培养产生的单克隆抗体,鉴定了狒狒精子发生过程中出现的精子抗原。通过蛋白质印迹法和免疫荧光技术确定,抗体BSA1和BSA2分别识别分子量为84,000和45,000道尔顿的胰蛋白酶敏感决定簇,它们分别局限于精子的尾部和顶体前部区域。在2岁和3岁的狒狒睾丸中不存在的尾部抗原,在大约4岁时首次出现在精子细胞中。相比之下,BSA2识别的顶体抗原存在于3岁的原始睾丸生殖细胞中。在成熟睾丸中,通过抗生物素蛋白-生物素免疫过氧化物酶法观察到,分子量为45,000的决定簇主要定位于粗线期晚期精母细胞和圆形精子细胞的细胞核中。抗体BSA3仅与成年睾丸经唾液酸酶处理的切片发生反应。这种抗胰蛋白酶的决定簇在睾丸精子上不表达,仅在附睾精子上被抗体BSA3识别,因此表明精子在睾丸后发生了修饰。