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机构地区:[1]温州市中西医结合医院检验科,浙江温州325000 [2]温州医学院附属第二医院不孕不育生殖健康中心,浙江温州325027
出 处:《中华男科学杂志》2008年第3期234-237,共4页National Journal of Andrology
摘 要:目的:探讨钙调蛋白是否参与小鼠精子获能过程。方法:用50、100、200μmol/L浓度的钙调蛋白抑制剂W7和10、20、30μmol/L浓度的钙调蛋白抑制剂卡米达佐(CZ)分别与小鼠精子孵育2h,通过金霉素染色法计算出B型精子百分率。并用100μmol/L钙调蛋白抑制剂W7和10μmol/LCZ分别与小鼠精子孵育2h后,再加入5μmol/L孕酮诱发顶体反应,计算精子顶体反应百分率。结果:不同浓度的W7和CZ作用小鼠精子,B型精子百分率呈浓度依赖性方式下降,与对照组比较,均有显著性差异(P<0.05)。顶体反应率与对照组相比均有极显著差异(P<0.01)。结论:钙调蛋白参与小鼠精子获能,是精子获能过程中的关键蛋白。Objective: To investigate the possible involvement of calmodulin in mouse sperm capacitation. Methods. Calmodulin antagnnists W7 at the concentrations of 50, 100 and 200μmol/L and calmidazolium (CZ) at the concentrations of 10, 20 and 30μmol/ L, were coincubated with mouse sperm for 2 hours, respectively. The percentage of pattern B sperm was measured by chloroteracycline staining. Then the sperm were coincubated with 100μmol/L W7 or 10μmol/L calmidazolium (CZ) before acrosome reaction was induced by 5μmol/L progesterone and evaluated by the same method. Results: After the treatment of the sperm with different concen-trations of CZ or W7, the percentages of pattern B sperm decreased in a dose-dependent manner, significantly different from the control (P 〈 0.05 ). There was a statistic difference in the rate of acrosome reaction between the experiment and the control group (P 〈 0.01 ). Conclusion : Calmodulin is a key protein involved in mouse sperm capacitation.
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