Chen Jing, Wang Yong, Xu Xiang, Yu Zhou, Gui Yao-ting, Cai Zhi-ming
Key Laboratory of Male Reproductive and Genetic Medicine, Shenzhen Hospital of Peking University, Shenzhen, Guangdong 518036, China.
Zhonghua Nan Ke Xue. 2009 Oct;15(10):891-4.
To compare the expressions of ODF1 (outer dense fiber of the sperm tail 1) in ejaculated spermatozoa from normozoospermic and asthenozoospermic men with low sperm motility.
Semen analyses were performed on the semen samples obtained from normozoospermic (n=20) and asthenozoospermic (n=20) volunteers according to the WHO criteria. To rule out the contamination of germ cells and leucocytes, the human ejaculated spermatozoa were purified by a discontinuous Percoll density gradient centrifugation. RT-PCR and Western blot were used to detect the expressions of ODF1 in the spermatozoa from the two groups.
RT-PCR showed that the expression of ODF1 mRNA was significantly lower in the spermatozoa from the asthenozoospermic patients than in those from the normozoospermic men (1.35 +/- 0.25 vs. 2.79 +/- 0.28, P < 0.05). Western blot confirmed the results from RT-PCR and revealed an obviously decreased expression of ODF1 in the spermatozoa of the asthenozoospermic patients, with statistically significant difference from the normozoospermic group (1.44 +/- 0.26 vs. 3.64 +/- 0.34, P < 0.05).
The expression of ODF1 was significantly decreased in the ejaculated spermatozoa of asthenozoospermic men, which might be responsible for low sperm motility.
比较正常精子活力男性与弱精子症男性射出精子中精子尾部外周致密纤维蛋白1(ODF1)的表达情况。
根据世界卫生组织标准,对从正常精子症(n = 20)和弱精子症(n = 20)志愿者获得的精液样本进行精液分析。为排除生殖细胞和白细胞的污染,通过不连续Percoll密度梯度离心法对人类射出精子进行纯化。采用逆转录-聚合酶链反应(RT-PCR)和蛋白质免疫印迹法检测两组精子中ODF1的表达。
RT-PCR显示,弱精子症患者精子中ODF1 mRNA的表达明显低于正常精子症男性(1.35±0.25对2.79±0.28,P < 0.05)。蛋白质免疫印迹法证实了RT-PCR的结果,并显示弱精子症患者精子中ODF1的表达明显降低,与正常精子症组相比有统计学差异(1.44±0.26对3.64±0.34,P < 0.05)。
弱精子症男性射出精子中ODF1的表达明显降低,这可能是精子活力低下的原因。