Joshi S A, Shaikh S, Ranpura S, Khole V V
Hybridoma Division, National Institute for Research in Reproductive Health, Jehangir Merwanji Street, Parel, Mumbai 400 012, India.
Reproduction. 2003 Apr;125(4):495-507. doi: 10.1530/rep.0.1250495.
A rat epididymal protein of 27 kDa was identified using neonatal tolerization. This study reports the production and characterization of a polyclonal antiserum to this protein. ELISA was used to demonstrate that this antiserum reacts strongly with epididymal sperm proteins, but has little or no reactivity with testicular proteins. Western blot analysis revealed that this polyclonal antiserum recognized a 27 kDa protein extracted from the corpus epididymidis as well as from spermatozoa from the corpus and cauda epididymides, and immunostaining revealed the presence of the protein in the corpus to cauda epididymides. Stronger reactivity was observed in the supranuclear region and stereocilla of principal cells of the corpus epididymidis and in the luminal content of the corpus and cauda epididymides. The testicular section showed no reactivity. Treatment with the antiserum resulted in time- and dose-dependent agglutination of rat spermatozoa. By indirect immunofluorescence, the antiserum localized proteins in the mid-piece region of rat spermatozoa. Studies were carried out to determine the age at which the protein first became apparent during postnatal development. The protein was expressed from day 40 onwards, as demonstrated by western blot analysis. The androgen regulation of this protein was ascertained by castration and supplementation studies. Expression of this protein showed a decline starting at day 14 after castration and by day 21 the protein was absent; however, androgen replacement resulted in the reappearance of the protein. The results of these studies indicate that the protein identified is specific to the epididymis, and is regulated by development and androgens. The importance of epididymis-specific proteins that are regulated by androgens in sperm maturation is discussed, and the need to ascertain the sequence of the protein and clone the cognate gene is indicated.
利用新生期耐受法鉴定出一种27 kDa的大鼠附睾蛋白。本研究报道了针对该蛋白的多克隆抗血清的制备及特性。采用酶联免疫吸附测定法(ELISA)证明,该抗血清与附睾精子蛋白反应强烈,但与睾丸蛋白反应微弱或无反应。蛋白质印迹分析显示,这种多克隆抗血清识别从附睾体以及附睾体和附睾尾精子中提取的一种27 kDa的蛋白质,免疫染色显示该蛋白存在于附睾体至附睾尾。在附睾体主细胞的核上区和静纤毛以及附睾体和附睾尾的管腔内容物中观察到更强的反应性。睾丸切片无反应性。用该抗血清处理导致大鼠精子出现时间和剂量依赖性凝集。通过间接免疫荧光法,该抗血清将蛋白质定位在大鼠精子的中段区域。开展研究以确定该蛋白在出生后发育过程中首次出现的年龄。蛋白质印迹分析表明,该蛋白从第40天开始表达。通过去势和补充研究确定了该蛋白的雄激素调节作用。该蛋白的表达在去势后第14天开始下降,到第21天该蛋白消失;然而,雄激素替代导致该蛋白重新出现。这些研究结果表明,所鉴定的蛋白是附睾特异性的,受发育和雄激素调节。讨论了受雄激素调节的附睾特异性蛋白在精子成熟中的重要性,并指出需要确定该蛋白的序列并克隆相关基因。