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利用不育患者的人抗精子抗体(ASA)鉴定进化保守的小鼠精子表面抗原。

Identification of evolutionary conserved mouse sperm surface antigens by human antisperm antibodies (ASA) from infertile patients.

作者信息

Paradowska Agnieszka, Bohring Claudia, Krause Eberhard, Krause Walter

机构信息

Department of Andrology, Clinical Training Center of the European Academy of Andrology, University Hospital Marburg, Marburg, Germany.

出版信息

Am J Reprod Immunol. 2006 May;55(5):321-30. doi: 10.1111/j.1600-0897.2006.00367.x.

Abstract

PROBLEM

The presence of antisperm antibodies (ASA) in semen may impair sperm function leading to immunological infertility. The aim of the study was to identify the evolutionary conserved antigens on mouse sperm surface that react with human ASA in order to study the mechanism of autoimmune infertility.

METHODS OF STUDY

The binding of human ASA to mouse sperm was investigated by means of indirect immunofluorescence. 2D-electrophoresis was applied to separate the biotin-labelled mouse membrane proteins using isoelectric focusing followed by polyacrylamide gel electrophoresis. Cognate antigens of ASA from seminal plasma of infertile patients were analysed by Western blotting. Performing avidin-blots it was detected which of the proteins recognized were sperm surface proteins. The spots of interest were analysed by means of mass spectrometry.

RESULTS

ASA bound most frequently (36%) to the post-acrosomal region and to the midpiece of mouse spermatozoa. About 30% of ASA recognized apo lactate dehydrogenase (LDHC4) as a cognate antigen, 30% voltage-dependent anion channel (VDAC2). ASA of 20% bound to outer dense fibre protein and 20% of samples recognized glutathione S-transferase mu5.

CONCLUSIONS

Human ASA bound to specific cognate antigens of mouse spermatozoa, offering the possibility to study their functional relevance in the mouse model.

摘要

问题

精液中抗精子抗体(ASA)的存在可能会损害精子功能,导致免疫性不孕。本研究的目的是鉴定小鼠精子表面与人类ASA发生反应的进化保守抗原,以研究自身免疫性不孕的机制。

研究方法

通过间接免疫荧光法研究人类ASA与小鼠精子的结合情况。采用二维电泳,先通过等电聚焦,再进行聚丙烯酰胺凝胶电泳,以分离生物素标记的小鼠膜蛋白。通过蛋白质印迹法分析不育患者精浆中ASA的同源抗原。进行抗生物素蛋白印迹,检测所识别的蛋白质中哪些是精子表面蛋白。通过质谱分析法对感兴趣的斑点进行分析。

结果

ASA最常(36%)与小鼠精子的顶体后区域和中段结合。约30%的ASA将载脂蛋白乳酸脱氢酶(LDHC4)识别为同源抗原,30%识别电压依赖性阴离子通道(VDAC2)。20%的ASA与外致密纤维蛋白结合,20%的样本识别谷胱甘肽S-转移酶μ5。

结论

人类ASA与小鼠精子的特定同源抗原结合,为在小鼠模型中研究它们的功能相关性提供了可能性。

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