Guo Xin, Gui Yao-Ting, Tang Ai-Fa, Lu Li-Hua, Gao Xin, Cai Zhi-Ming
The Laboratory of Male Reproductive Medicine, Peking University Shenzhen Hospital, Shenzhen 518036, China.
Asian J Androl. 2007 May;9(3):339-44. doi: 10.1111/j.1745-7262.2007.00253.x.
To detect the expression of VASA in human ejaculated spermatozoa, and to compare the expression of VASA between normozoospermic men and patients with oligozoospermia.
Ejaculated spermatozoa were collected from normozoospermic men and patients with oligozoospermia by masturbation, and subsequently segregated through a discontinuous gradient of Percoll to obtain the spermatozoa. Reverse transcription polymerase chain reaction (RT-PCR), quantitative RT-PCR (QRT-PCR), immunoflurescence and Western blotting were used to detect the expression of VASA in mRNA and protein levels.
VASA mRNA was expressed in the ejaculated spermatozoa. QRT-PCR analysis showed that VASA mRNA level was approximately 5-fold higher in normozoospermic men than that in oligozoospermic men. Immunofluorescence and Western blotting analysis showed that VASA protein was located on the cytoplasmic membrane of heads and tails of spermatozoa, and its expression was significantly decreased in oligozoospermic men, which is similar to the result of QRT-PCR.
The expression of VASA mRNA and protein was significantly decreased in the sperm of oligozoospermic men, which suggested the lower expression of the VASA gene might be associated with pathogenesis in some subtypes of male infertility and VASA could be used as a molecular marker for the diagnosis of male infertility.
检测VASA在人类射出精子中的表达,并比较正常精子症男性与少精子症患者中VASA的表达情况。
通过手淫从正常精子症男性和少精子症患者中收集射出精子,随后通过不连续的Percoll梯度离心进行分离以获得精子。采用逆转录聚合酶链反应(RT-PCR)、定量RT-PCR(QRT-PCR)、免疫荧光和蛋白质印迹法检测VASA在mRNA和蛋白质水平的表达。
VASA mRNA在射出精子中表达。QRT-PCR分析显示,正常精子症男性中VASA mRNA水平比少精子症男性高约5倍。免疫荧光和蛋白质印迹分析表明,VASA蛋白位于精子头部和尾部的细胞膜上,其在少精子症男性中的表达显著降低,这与QRT-PCR结果相似。
少精子症男性精子中VASA mRNA和蛋白质的表达显著降低,这表明VASA基因表达降低可能与某些男性不育亚型的发病机制有关,且VASA可作为男性不育诊断的分子标志物。