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Inhibition of mouse acrosome reaction and sperm-zona pellucida binding by anti-human sperm membrane protein 1 antibody

机译:抗人精子膜蛋白1抗体抑制小鼠顶体反应和精子-透明带结合

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摘要

Aim: To investigate the possible functions of human sperm membrane protein (hSMP-1) in the process of fertilization. Methods: A 576-bp cDNA fragment of HSD-1 gene coding for the extracellular domain of hSMP-1 was cloned and expressed. The localization of this protein on human and mouse sperm was determined by indirect immunofluores-cent staining by using anti-recombinant hSMP-1 (anti-rhSMP-1) antibodies. Sperm acrosome reaction and sperm-zona pellucida (ZP) binding assay were carried out in 10-week-old BALB/c mice. Results: Recombinant hSMP-1 was successfully cloned and expressed. The expression of the native protein was limited on the acrosome of human and mouse sperm. Treatment of anti-rhSMP-1 antibodies significantly decreased the average number of sperms bound to each egg. Meanwhile, the percentage of acrosome reaction was decreased in comparison to pre-immune control after treatment with anti-rhSMP-1 (P < 0.05). Conclusion: The results suggest that anti-rhSMP-1 antibody inhibited mouse acrosome reaction and sperm-ZP binding.
机译:目的:探讨人精子膜蛋白(hSMP-1)在受精过程中的可能功能。方法:克隆并表达了HSD-1基因的576bp cDNA片段,该片段编码hSMP-1的胞外域。通过使用抗重组hSMP-1(anti-rhSMP-1)抗体通过间接免疫荧光染色确定该蛋白在人和小鼠精子上的定位。在10周大的BALB / c小鼠中进行了精子顶体反应和sperm-zona pellucida(ZP)结合测定。结果:成功克隆并表达了重组hSMP-1。天然蛋白的表达仅限于人和小鼠精子的顶体。抗rhSMP-1抗体的治疗显着降低了每个卵子结合的平均精子数量。同时,与抗rhSMP-1治疗后的免疫前对照相比,顶体反应的百分比降低了(P <0.05)。结论:结果表明抗rhSMP-1抗体抑制小鼠顶体反应和精子ZP结合。

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