Priority Research Centre for Reproductive Science, School of Environmental and Life Sciences, Discipline of Biological Sciences, The University of Newcastle, Callaghan, NSW, Australia; Pregnancy and Reproduction Program, Hunter Medical Research Institute, New Lambton Heights, NSW, Australia.
Priority Research Centre for Reproductive Science, School of Environmental and Life Sciences, Discipline of Biological Sciences, The University of Newcastle, Callaghan, NSW, Australia; Pregnancy and Reproduction Program, Hunter Medical Research Institute, New Lambton Heights, NSW, Australia; Department of Biochemistry and Cell Biology, Faculty of Veterinary Medicine, Utrecht University, Utrecht, The Netherlands.
Mol Cell Proteomics. 2021;20:100107. doi: 10.1016/j.mcpro.2021.100107. Epub 2021 Jun 2.
Seminal vesicles are an integral part of the male reproductive accessory gland system. They produce a complex array of secretions containing bioactive constituents that support gamete function and promote reproductive success, with emerging evidence suggesting these secretions are influenced by our environment. Despite their significance, the biology of seminal vesicles remains poorly defined. Here, we complete the first proteomic assessment of mouse seminal vesicles and assess the impact of the reproductive toxicant acrylamide. Mice were administered acrylamide (25 mg/kg bw/day) or control daily for five consecutive days prior to collecting seminal vesicle tissue. A total of 5013 proteins were identified in the seminal vesicle proteome with bioinformatic analyses identifying cell proliferation, protein synthesis, cellular death, and survival pathways as prominent biological processes. Secreted proteins were among the most abundant, and several proteins are linked with seminal vesicle phenotypes. Analysis of the effect of acrylamide on the seminal vesicle proteome revealed 311 differentially regulated (FC ± 1.5, p ≤ 0.05, 205 up-regulated, 106 downregulated) proteins, orthogonally validated via immunoblotting and immunohistochemistry. Pathways that initiate protein synthesis to promote cellular survival were prominent among the dysregulated pathways, and rapamycin-insensitive companion of mTOR (RICTOR, p = 6.69E-07) was a top-ranked upstream driver. Oxidative stress was implicated as contributing to protein changes, with acrylamide causing an increase in 8-OHdG in seminal vesicle epithelial cells (fivefold increase, p = 0.016) and the surrounding smooth muscle layer (twofold increase, p = 0.043). Additionally, acrylamide treatment caused a reduction in seminal vesicle secretion weight (36% reduction, p = 0.009) and total protein content (25% reduction, p = 0.017). Together these findings support the interpretation that toxicant exposure influences male accessory gland physiology and highlights the need to consider the response of all male reproductive tract tissues when interpreting the impact of environmental stressors on male reproductive function.
精囊是男性生殖附属腺体系统的一个组成部分。它们产生一系列复杂的分泌物,其中包含支持配子功能和促进生殖成功的生物活性成分,有新的证据表明这些分泌物受我们的环境影响。尽管它们很重要,但精囊的生物学特性仍未得到很好的定义。在这里,我们完成了对小鼠精囊的首次蛋白质组学评估,并评估了生殖毒物丙烯酰胺的影响。小鼠在连续 5 天每天接受 25mg/kg bw 的丙烯酰胺或对照处理,然后收集精囊组织。在精囊蛋白质组中鉴定出 5013 种蛋白质,生物信息学分析确定细胞增殖、蛋白质合成、细胞死亡和存活途径为突出的生物学过程。分泌蛋白是最丰富的蛋白之一,其中一些蛋白与精囊表型有关。分析丙烯酰胺对精囊蛋白质组的影响,发现 311 种差异调节的蛋白质(FC ± 1.5,p ≤ 0.05,205 种上调,106 种下调),通过免疫印迹和免疫组织化学正交验证。在失调的途径中,启动蛋白质合成以促进细胞存活的途径最为突出,雷帕霉素不敏感的 mTOR 伴侣(RICTOR,p = 6.69E-07)是排名最高的上游驱动因素。氧化应激被认为是导致蛋白质变化的原因,丙烯酰胺导致精囊上皮细胞(增加 5 倍,p = 0.016)和周围平滑肌层(增加 2 倍,p = 0.043)中的 8-OHdG 增加。此外,丙烯酰胺处理导致精囊分泌重量(减少 36%,p = 0.009)和总蛋白含量(减少 25%,p = 0.017)减少。这些发现共同支持这样的解释,即有毒物质暴露会影响男性附属腺体的生理学,并强调在解释环境应激对男性生殖功能的影响时,需要考虑所有男性生殖道组织的反应。