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TASK-1、TRAAK蛋白在弱精子症患者精子中的表达

Expression of TASK-1,TRAAK protein in the ejaculated spermatozoa of asthenozoospermic men
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摘要 目的探讨双孔钾离子通道TASK-1、TRAAK蛋白在精子中的表达及其在弱精子症发生机制中的作用。方法非连续密度梯度离心分离、纯化正常男性和弱精子症患者精子后,采用Western印迹技术从蛋白水平检测TASK-1、TRAAK的表达及差异。结果 TASK-1、TRAAK蛋白在正常男性和弱精子症患者精子中均有表达;其中,TASK-1蛋白在弱精子症患者精子中的表达量与正常男性没有明显差异(P>0.05),TRAAK蛋白在弱精子症患者精子中的表达明显低于常男性(P<0.05),这与我们前期的RT-PCR结果一致。结论 TRAAK在弱精子症患者精子中的表达下调可能是精子活力下降的原因之一。 Objective:To investigate the expression of K2 P channel TASK-1、TRAAK protein in the sperm and the role of them in the pathogenesis of asthenozoospermia. Methods:Semen samples from 23 normal male persons and 35 asthenozoospermia patients were separated and purified by Percoll discontinuous density gradients and the expressions of TASK-1、TRAAK protein were detected by Western blot. Results:TASK-1,TRAAK protein were expressed in the sperm both in the normal male persons and the asthenozoospermia patients;the expression of TRAAK protein was significantly lower in the sperm of the asthenozoospermia patients than in those of the normal male persons(P〈0.05),while,there was no significant difference of TASK-1 protein in the two groups(P〉0.05),the results are consistent with our previous RT-PCR experiment. Conclusion:The expression of TRAAK is significantly decreased in the sperm of asthenozoospermia patients,which might be one of the causes of Sperm vitality decline.
出处 《中国优生与遗传杂志》 2017年第9期112-114,共3页 Chinese Journal of Birth Health & Heredity
基金 湖北省卫生计生科研项目基金资助(WJ2015MB254)
关键词 双孔钾离子通道 TASK-1蛋白 TRAAK蛋白 弱精子症 免疫印迹 K2P channels TASK-1 protein TRAAKprotein Asthenozoospermia Western blot
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