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首页> 外文期刊>Human Reproduction >Tyrosine phosphorylation on capacitated human sperm tail detected by immunofluorescence correlates strongly with sperm-zona pellucida (ZP) binding but not with the ZP-induced acrosome reaction.
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Tyrosine phosphorylation on capacitated human sperm tail detected by immunofluorescence correlates strongly with sperm-zona pellucida (ZP) binding but not with the ZP-induced acrosome reaction.

机译:通过免疫荧光检测,在获能的人类精子尾巴上的酪氨酸磷酸化与精子-透明带(ZP)的结合密切相关,但与ZP诱导的顶体反应却不相关。

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摘要

BACKGROUND: Protein tyrosine phosphorylation (TP) of human sperm is related to sperm capacitation and zona pellucida (ZP) binding. The aim of this study was to determine whether the TP of capacitated sperm is a useful marker for the ability of sperm to bind to the ZP and undergo the ZP-induced acrosome reaction (AR). METHODS: Semen samples were obtained from 115 subfertile men with sperm count > or =20 x 10(6)/ml, motility > or =25% and variable morphology. Motile sperm (2 x 10(6)/ml) selected by swim-up were incubated with four oocytes for 2 h, and the number of sperm bound to the ZP and the ZP-induced AR was examined. TP of sperm tail was assessed by immunofluorescence (IF) with anti-phosphotyrosine monoclonal antibody. The time course and effects of dibutyryl cyclic adenosine monophosphate (dbcAMP) and phorbol myristate acetate (PMA) on TP were also studied. RESULTS: TP was stimulated more by dbcAMP (P < 0.001) and less by PMA (P < 0.05). TP increased significantly with time of incubation of sperm. TP was not detectable on the surface of unfixed live sperm by either Dynabeads or IF. Sperm TP at 2, 4 and 20 h incubation was all significantly correlated with sperm-ZP binding but not with the ZP-induced AR. CONCLUSION: Sperm TP detected by IF correlates strongly with sperm-ZP binding capacity but not with the ZP-induced AR. This simple IF assay of TP may be a clinically useful test of sperm function that is predictive of normal sperm ZP-binding capacity.
机译:背景:人类精子的蛋白质酪氨酸磷酸化(TP)与精子获能和透明带(Zona pellucida,ZP)结合有关。这项研究的目的是确定获能的精子的TP是否是精子结合ZP并进行ZP诱导的顶体反应(AR)的能力的有用标记。方法:从115名精子数量大于或等于20 x 10(6)/ ml,运动性大于或等于25%且形态变化的男性中提取精液样本。通过游泳选择的运动精子(2 x 10(6)/ ml)与四个卵母细胞一起孵育2小时,并检查与ZP和ZP诱导的AR结合的精子数量。用抗磷酸酪氨酸单克隆抗体通过免疫荧光(IF)评估精子尾巴的TP。还研究了二丁酰基环状单磷酸腺苷(dbcAMP)和佛波醇肉豆蔻酸酯乙酸(PMA)的时程及对TP的影响。结果:dbcAMP刺激TP更多(P <0.001),PMA刺激更少(P <0.05)。随着精子潜伏时间的延长,TP显着增加。 Dynabeads或IF无法在未固定的活精子表面检测到TP。在孵育2、4和20 h时,精子TP均与精子与ZP的结合显着相关,但与ZP诱导的AR无关。结论:IF检测到的精子TP与精子-ZP结合能力强相关,而与ZP诱导的AR无关。 TP的这种简单的IF分析可能是精子功能的临床有用测试,可预测正常的精子ZP结合能力。

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