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精液、精子膜蛋白和精细胞外囊泡的定量蛋白质组学分析表明,囊泡机制有助于去除和添加蛋白质到公羊精子膜。

Quantitative Proteomic Analysis of Seminal Plasma, Sperm Membrane Proteins, and Seminal Extracellular Vesicles Suggests Vesicular Mechanisms Aid in the Removal and Addition of Proteins to the Ram Sperm Membrane.

机构信息

School of Life and Environmental Sciences, Faculty of Science, University of Sydney, Sydney, New South Wales, 2006, Australia.

Colorado Center for Reproductive Medicine, Lone Tree, Colorado, 80124, USA.

出版信息

Proteomics. 2020 Jun;20(12):e1900289. doi: 10.1002/pmic.201900289. Epub 2020 Jun 8.

DOI:10.1002/pmic.201900289
PMID:32383290
Abstract

Quantitative proteomic studies are contributing greatly to the understanding of the spermatozoon through the provision of detailed information on the proteins spermatozoa acquire and shed in the acquisition of fertility. Extracellular vesicles (EVs) are thought to aid in the delivery of proteins to spermatozoa in the male reproductive tract. The aim of this study is to isolate, identify and quantify EV proteins isolated from ram seminal plasma. Ram sperm plasma membrane proteins are also isolated using nitrogen cavitation and identified to better understand the interplay of proteins between the sperm membrane and extracellular environment. The categorization of proteins enriched in the EV population according to their function revealed three main groupings: vesicle biogenesis, metabolism, and membrane adhesion and remodeling. The latter group contains many reproduction-specific proteins that show demonstrable links to sperm fertility. Many of these membrane-bound proteins show testicular expression and are shed from the sperm surface during epididymal maturation (e.g., testis expressed 101; TEX101 and lymphocyte Antigen 6 Family Member K; LY6K). Their association with seminal EVs suggests that EVs may not only deliver protein cargo to spermatozoa but also assist in the removal of proteins from the sperm membrane.

摘要

定量蛋白质组学研究通过提供有关精子在获得生育能力过程中获得和释放的蛋白质的详细信息,极大地促进了对精子的理解。细胞外囊泡(EVs)被认为有助于将蛋白质递送至雄性生殖道中的精子。本研究旨在从公羊精液中分离、鉴定和定量 EV 蛋白。还使用氮空化分离公羊精子质膜蛋白,并对其进行鉴定,以更好地了解精子膜与细胞外环境之间蛋白质的相互作用。根据功能对 EV 群体中富集的蛋白质进行分类,揭示了三个主要分组:囊泡发生、代谢以及膜粘附和重塑。后一组包含许多与精子生育力有明显联系的特定于生殖的蛋白质。许多这些膜结合蛋白显示睾丸表达,并在附睾成熟过程中从精子表面脱落(例如,睾丸表达 101;TEX101 和淋巴细胞抗原 6 家族成员 K;LY6K)。它们与精液 EV 的关联表明,EV 不仅可以向精子输送蛋白质货物,还可以帮助从精子膜上去除蛋白质。

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