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作 者:陈静[1] 王勇[1,2] 许祥[1] 余州[1] 桂耀庭[1] 蔡志明[1]
机构地区:[1]北京大学深圳医院男性生殖与遗传重点实验室,广东深圳518036 [2]汕头大学医学院生理系,广东汕头515041
出 处:《中华男科学杂志》2009年第10期891-894,共4页National Journal of Andrology
基 金:国家自然科学基金(30770810);广东省科技计划项目(2007B060401061);深圳市科技计划项目(200903078)~~
摘 要:目的:比较外周致密纤维1(ODF1)在健康男性和弱精子症患者精子中的表达差异。方法:根据WHO标准,收集正常男性和弱精子症患者的精液标本各20份,Percoll非连续梯度离心法分离精子,收集95%Percoll以下和57%与76%Percoll层之间的精子,以排除生精细胞和白细胞的污染;采用逆转录-多聚酶链式反应(RT-PCR)和Western印迹方法,从mRNA和蛋白水平检测ODF1的表达。结果:RT-PCR结果表明,与正常男性组相比,ODF1在弱精子症患者精子中的mRNA表达水平显著降低(2.79±0.28vs1.35±0.25,P<0.05);免疫印迹与RT-PCR结果一致,与正常男性组相比,弱精子症患者精子中的ODF1蛋白的表达亦显著降低(3.64±0.34vs1.44±0.26,P<0.05)。结论:ODF1在弱精子症患者精子中的表达显著降低,提示其可能与精子活动力低下有关。Objective: 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.Methods: 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.Results: 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).Conclusion: The expression of ODF1 was significantly decreased in the ejaculated spermatozoa of asthenozoospermic men,which might be responsible for low sperm motility.
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