Wu Wen-bin, Li Yu-shan, Feng Xiao-xia, Wang Quan-xian, Gao Xue-min, Yang Xian-feng, Pan Zhou-hui, Sun Lin
Human Sperm Bank, The Third Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan 450052, China.
Zhonghua Nan Ke Xue. 2011 Feb;17(2):110-4.
To investigate the role of the cation channel of sperm 1 (CatSper1) protein in the pathogenesis of idiopathic asthenozoospermia.
Sperm samples from patients with idiopathic asthenozoospermia were separated by Percoll discontinuous density gradients, and the distribution and expression of the CatSper1 protein were determined by immunocytochemistry. Western blotting was used to detect the different expressions of CatSper1 in the ejaculated sperm from the normal control, mild asthenozoospermia, moderate asthenozoospermia and severe asthenozoospermia groups, followed by statistical analyses.
The expression of CatSper1, located in the principle piece of the sperm tail, was reduced significantly in the samples from the idiopathic asthenozoospermia patients as compared with the normal controls (t = 2.188, P = 0.042). The relative contents of the CatSper1 protein in the sperm of the control, mild asthenozoospermia, moderate asthenozoospermia and severe asthenozoospermia groups were 0.806 +/- 0.266, 0.669 +/- 0.207, 0.505 +/- 0.214 and 0.295 +/- 0.162, respectively, significantly decreased in the asthenozoospermia patients in comparison with the normal controls (P <0.05). There was a positive correlation between the percentage of progressively motile sperm and the relative content of the CatSper1 protein (r = 0.633, P = 0.000).
The decreased or abnormal expression of the CatSper1 protein may be a factor involved in the pathogenesis of idiopathic asthenozoospermia.
探讨精子阳离子通道蛋白1(CatSper1)在特发性弱精子症发病机制中的作用。
采用Percoll不连续密度梯度法分离特发性弱精子症患者的精液样本,通过免疫细胞化学法检测CatSper1蛋白的分布及表达情况。采用蛋白质印迹法检测正常对照组、轻度弱精子症组、中度弱精子症组和重度弱精子症组射精精子中CatSper1的表达差异,并进行统计学分析。
与正常对照组相比,特发性弱精子症患者样本中位于精子尾部主段的CatSper1表达显著降低(t = 2.188,P = 0.042)。对照组、轻度弱精子症组、中度弱精子症组和重度弱精子症组精子中CatSper1蛋白的相对含量分别为0.806±0.266、0.669±0.207、0.505±0.214和0.295±0.162,弱精子症患者与正常对照组相比显著降低(P <0.05)。进行性运动精子百分比与CatSper1蛋白相对含量呈正相关(r = 0.633,P = 0.000)。
CatSper1蛋白表达降低或异常可能是特发性弱精子症发病机制的一个因素。