From the ‡Priority Research Centre for Reproductive Science, School of Environmental and Life Sciences, Discipline of Biological Sciences, The University of Newcastle, University Drive, Callaghan, NSW 2308, Australia.
From the ‡Priority Research Centre for Reproductive Science, School of Environmental and Life Sciences, Discipline of Biological Sciences, The University of Newcastle, University Drive, Callaghan, NSW 2308, Australia;; School of Biomedical Sciences and Pharmacy, Faculty of Health and Medicine, The University of Newcastle, Callaghan, NSW 2308, Australia.
Mol Cell Proteomics. 2019 Mar 15;18(Suppl 1):S91-S108. doi: 10.1074/mcp.RA118.000946. Epub 2018 Sep 13.
The functional maturation of spermatozoa that is necessary to achieve fertilization occurs as these cells transit through the epididymis, a highly specialized region of the male reproductive tract. A defining feature of this maturation process is that it occurs in the complete absence of nuclear gene transcription or , protein translation in the spermatozoa. Rather, it is driven by sequential interactions between spermatozoa and the complex external milieu in which they are bathed within lumen of the epididymal tubule. A feature of this dynamic microenvironment are epididymosomes, small membrane encapsulated vesicles that are secreted from the epididymal soma. Herein, we report comparative proteomic profiling of epididymosomes isolated from different segments of the mouse epididymis using multiplexed tandem mass tag (TMT) based quantification coupled with high resolution LC-MS/MS. A total of 1640 epididymosome proteins were identified and quantified via this proteomic method. Notably, this analysis revealed pronounced segment-to-segment variation in the encapsulated epididymosome proteome. Thus, 146 proteins were identified as being differentially accumulated between caput and corpus epididymosomes, and a further 344 were differentially accumulated between corpus and cauda epididymosomes (, fold change of ≤ -1.5 or ≥ 1.5; , < 0.05). Application of gene ontology annotation revealed a substantial portion of the epididymosome proteins mapped to the cellular component of extracellular exosome and to the biological processes of transport, oxidation-reduction, and metabolism. Additional annotation of the subset of epididymosome proteins that have not previously been identified in exosomes revealed enrichment of categories associated with the acquisition of sperm function (, fertilization and binding to the zona pellucida). In tandem with our demonstration that epididymosomes are able to convey protein cargo to the head of maturing spermatozoa, these data emphasize the fundamental importance of epididymosomes as key elements of the epididymal microenvironment responsible for coordinating post-testicular sperm maturation.
精子实现受精所必需的功能成熟是在穿过附睾时发生的,附睾是男性生殖道的一个高度专业化区域。这个成熟过程的一个定义特征是,它发生在精子中核基因转录或蛋白质翻译完全缺失的情况下。相反,它是由精子与它们在附睾管腔中浸泡的复杂外部环境之间的连续相互作用驱动的。这个动态微环境的一个特征是附睾小体,这是从小体分泌的小膜包裹囊泡。在此,我们使用多重串联质量标签(TMT)基于定量的方法联合高分辨率 LC-MS/MS 报告了从小鼠附睾不同节段分离的附睾小体的比较蛋白质组学分析。通过这种蛋白质组学方法鉴定和定量了 1640 种附睾小体蛋白。值得注意的是,这种分析显示出包裹的附睾小体蛋白质组在节段到节段之间存在明显的变化。因此,在头部和体部附睾小体之间有 146 种蛋白被鉴定为差异积累,在体部和尾部附睾小体之间有 344 种蛋白被鉴定为差异积累(,变化倍数≤-1.5 或≥1.5;,<0.05)。GO 注释的应用表明,附睾小体蛋白的很大一部分映射到细胞外外泌体的细胞成分,以及运输、氧化还原和代谢等生物学过程。对以前未在 exosomes 中鉴定到的附睾小体蛋白子集的进一步注释表明,与精子功能获得(,受精和与透明带结合)相关的类别富集。与我们证明附睾小体能够将蛋白质货物递送到成熟精子的头部相吻合,这些数据强调了附睾小体作为负责协调附后精子成熟的附睾微环境关键因素的基本重要性。