Barranco Isabel, Martínez-Díaz Pablo, Parra Ana, Martínez-Alborcia María José, Lucas Xiomara, Rodríguez-Martínez Heriberto, Roca Jordi
Department of Medicine and Animal Surgery, Faculty of Veterinary Science, University of Murcia, Murcia, Spain.
Topigs Norsvin, Las Rozas, Madrid, Spain.
Andrology. 2025 Jul 4. doi: 10.1111/andr.70089.
Predicting male fertility in farm animals remains a challenge. Seminal plasma (SP) contains a high amount of heterogeneous seminal extracellular vesicles (sEVs), believed involved in reproductive processes and maybe key to understanding male fertility.
To identify the sEV proteins that are differentially expressed between more and less fertile boars and that could be candidates for fertility biomarkers in boars used in artificial insemination (AI) programs.
Small (S) and large (L) sEV subsets from SP samples of AI boars with differences in fertility: high (H) or low (L) farrowing rate (FR) and large (L) or small (S) litter size (LS). The S- and L-sEV subsets were isolated by size exclusion chromatography and characterized according to the Minimal Information for Studies of Extracellular Vesicles (MISEV2023) guidelines. Proteomic analyses (three biological replicates per fertility group and sEV subset) were performed using a Bruker timsTOF fleX™ instrument with data-independent acquisition parallel accumulation-serial fragmentation (diaPASEF) technology.
A total of 470 and 726 proteins were quantified in S-sEVs and 1801 and 1834 proteins in L-sEVs from FR and LS boars, respectively. Differentially expressed sEV proteins (logfold change ≥±1, p ≤ 0.05 and effect size d of Cohen >2.0) were found between the fertility groups: seven in S-sEVs and 52 in L-sEVs between H-FR and L-FR boars, and 47 in S-sEVs and 52 in L-sEVs between L-LS and S-LS boars. Many of these differentially expressed sEV proteins are involved in reproductive processes, particularly in sperm function and sperm-zona pellucida binding, but also in embryo development and implantation.
The sEV proteome differs between more and less fertile boars, with many of the differentially expressed proteins known as involved in reproductive processes. This would suggest that sEVs may be involved in male fertility and that some of the differentially expressed sEV proteins could be potential fertility markers for AI boars.
预测家畜的雄性生育能力仍然是一项挑战。精浆(SP)含有大量异质性的精液细胞外囊泡(sEVs),据信其参与生殖过程,可能是理解雄性生育能力的关键。
鉴定在生育能力较强和较弱的公猪之间差异表达的sEV蛋白,这些蛋白可能是用于人工授精(AI)计划的公猪生育能力生物标志物的候选物。
从生育能力存在差异的人工授精公猪的SP样本中分离出小(S)和大(L)sEV亚群:高(H)或低(L)产仔率(FR)以及大(L)或小(S)窝产仔数(LS)。通过尺寸排阻色谱法分离S-和L-sEV亚群,并根据细胞外囊泡研究的最低信息(MISEV2023)指南进行表征。使用配备数据非依赖采集平行累积-串联碎裂(diaPASEF)技术的布鲁克timsTOF fleX™仪器进行蛋白质组学分析(每个生育组和sEV亚群进行三次生物学重复)。
在FR和LS公猪的S-sEVs中分别定量了470和726种蛋白质,在L-sEVs中分别定量了1801和1834种蛋白质。在生育能力不同的组之间发现了差异表达的sEV蛋白(对数倍变化≥±1,p≤0.05且科恩效应大小d>2.0):在H-FR和L-FR公猪之间,S-sEVs中有7种,L-sEVs中有52种;在L-LS和S-LS公猪之间,S-sEVs中有47种,L-sEVs中有52种。这些差异表达的sEV蛋白中有许多参与生殖过程,特别是精子功能和精子-透明带结合,也参与胚胎发育和着床。
生育能力较强和较弱的公猪之间的sEV蛋白质组不同,许多差异表达的蛋白质已知参与生殖过程。这表明sEVs可能参与雄性生育能力,并且一些差异表达的sEV蛋白可能是人工授精公猪潜在的生育标志物。