Zhang Jingjing, Wu Jindao, Huo Ran, Mao Yingzi, Lu Ying, Guo Xuejiang, Liu Jiayin, Zhou Zuomin, Huang Xiaoyan, Sha Jiahao
Laboratory of Reproductive Medicine, Department of Histology and Embryology, Nanjing Medical University, Nanjing 210029, Jiangsu, PR China.
Mol Hum Reprod. 2007 Sep;13(9):633-9. doi: 10.1093/molehr/gam049. Epub 2007 Aug 17.
Human infertility is a growing concern and while many assisted reproductive technologies exist, their success rates are low. Thus, developing tests, possibly by assessing proteins involved in fertilization, that could predict the outcome of these technologies is of great significance. To identify candidate proteins, we used two-dimensional polyacrylamide gel electrophoresis and MALDI-TOF techniques and detected the ERp57 protein from human testis protein profile. Immunohistochemistry showed that ERp57 was mostly located in spermatogenic cell cytoplasm from spermatocytes to the spermatozoa phases and in Leydig cells of human testes; it was also present at low levels in Sertoli cells. ERp57 was evident in human spermatozoa, primarily in the acrosome and tail; moreover, it appeared to translocate to the equatorial segment after the acrosome reaction. During sperm capacitation, the ERp57 protein underwent post-translational modification. Blocking ERp57 with antibodies significantly inhibited human sperm from penetrating zona-free hamster oocytes in a dose-dependent manner. Finally, expression levels of ERp57 were associated with fertility; they were decreased dramatically in IVF patients with low fertilization rates compared with those with high rates or to fertile sperm donors. Taken together, these results show that ERp57 is a component of human sperm acrosome proteins, which play a critical role in gamete fusion. Furthermore, ERp57 could be a novel phenotype marker for male infertility and has the potential to be used to assess sperm selection for IVF.
人类不育问题日益受到关注,尽管存在多种辅助生殖技术,但其成功率较低。因此,开发可能通过评估受精过程中涉及的蛋白质来预测这些技术结果的检测方法具有重要意义。为了鉴定候选蛋白质,我们使用二维聚丙烯酰胺凝胶电泳和基质辅助激光解吸电离飞行时间质谱技术,从人睾丸蛋白质谱中检测到了ERp57蛋白。免疫组织化学显示,ERp57主要定位于人睾丸从精母细胞到精子阶段的生精细胞质以及睾丸间质细胞中;在支持细胞中也有低水平表达。ERp57在人精子中明显存在,主要位于顶体和尾部;此外,在顶体反应后它似乎转移到了赤道段。在精子获能过程中,ERp57蛋白发生了翻译后修饰。用抗体阻断ERp57能以剂量依赖的方式显著抑制人精子穿透去透明带仓鼠卵母细胞。最后,ERp57的表达水平与生育能力相关;与高受精率的体外受精患者或可育精子供体相比,低受精率的体外受精患者中其表达水平显著降低。综上所述,这些结果表明ERp57是人精子顶体蛋白的一个组成部分,在配子融合中起关键作用。此外,ERp57可能是男性不育的一种新型表型标志物,有潜力用于评估体外受精的精子选择。