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深入分析少弱精症和正常精子精液中的蛋白质组。

In-depth quantitative proteome analysis of seminal plasma from men with oligoasthenozoospermia and normozoospermia.

机构信息

Central LaboratoryThe Affiliated Yantai Yuhuangding Hospital of Qingdao UniversityYantaiShandong264000People's Republic of China.

Central LaboratoryThe Affiliated Yantai Yuhuangding Hospital of Qingdao UniversityYantaiShandong264000People's Republic of China; Department of Clinical LaboratoryThe Affiliated Yantai Yuhuangding Hospital of Qingdao UniversityYantaiShandong264000People's Republic of China.

出版信息

Reprod Biomed Online. 2018 Oct;37(4):467-479. doi: 10.1016/j.rbmo.2018.06.025. Epub 2018 Jul 19.

Abstract

RESEARCH QUESTION

Can seminal plasma markers for oligoasthenozoospermia be identified by comparison of the human seminal plasma proteome in men with oligoasthenozoospermia and normozoospermia?

DESIGN

An in-depth quantitative proteome analysis was conducted using a high-throughput method named isobaric tag for relative and absolute quantification. A total of 734 seminal plasma proteins were quantified by mass spectrometry.

RESULTS

Compared with the seminal plasma from men with normozoospermia, 22 upregulated proteins and 20 downregulated proteins were identified in the oligoasthenozoospermic seminal plasma. These differential seminal plasma proteins were involved in various physiological processes, including metabolism, transport, antioxidation and immune response. The confidence of some proteome data was further verified by western blot of (prostate-specific antigen [KLK3], lactotransferrin [LTF], alpha-1-antitrypsin [SERPINA1] and glyceraldehyde-3-phosphate dehydrogenase [GAPDH]). Additionally, 38% of the seminal plasma proteins identified in this study have not been reported in previously published studies on seminal plasma proteome, and 53% of our seminal plasma proteins were shared with published studies on human plasma proteome.

CONCLUSIONS

Our seminal plasma proteome research provides new complementary high-confidence data, and also enhances understanding of the pathogenic mechanisms in oligoasthenozoospermia.

摘要

研究问题

通过比较少精子症和正常精子症患者的人精液蛋白质组,能否鉴定出少精子症的精液标志物?

设计

使用一种名为相对和绝对定量标记的高通量方法进行深入的定量蛋白质组分析。通过质谱共定量了 734 种精液蛋白质。

结果

与正常精子症患者的精液相比,在少精子症患者的精液中鉴定出 22 种上调蛋白和 20 种下调蛋白。这些差异表达的精液蛋白质参与了各种生理过程,包括代谢、运输、抗氧化和免疫反应。一些蛋白质组数据的可信度通过 Western blot 进一步验证(前列腺特异性抗原[KLK3]、乳转铁蛋白[LTF]、α-1-抗胰蛋白酶[SERPINA1]和甘油醛-3-磷酸脱氢酶[GAPDH])。此外,本研究中鉴定的 38%的精液蛋白质以前在发表的精液蛋白质组研究中没有报道过,而我们的 53%的精液蛋白质与已发表的人类血浆蛋白质组研究中共享。

结论

我们的精液蛋白质组研究提供了新的补充性高可信度数据,也增强了对少精子症发病机制的理解。

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