Urological Research Institute, Division of Experimental Oncology, IRCCS San Raffaele Scientific Institute, Milano, Italy.
Centro Scienze Natalità, Obstetrics and Gynecology Unit, IRCCS San Raffaele Scientific Institute, Milano, Italy.
Hum Reprod. 2019 Aug 1;34(8):1416-1427. doi: 10.1093/humrep/dez114.
Are there differences in the proteomic profile of exosomes isolated from seminal plasma of normozoospermic (NSP) and severe asthenozoospermic (SA) men, potentially contributing to sperm features?
A relevant group of proteins known to positively regulate sperm functions were over-represented in seminal exosomes of NSP men, i.e. cysteine-rich secretory protein-1 (CRISP1), while the inhibitory protein glycodelin was enriched in exosomes of SA subjects.
Exosomes are secreted along the male reproductive tract and are thought to be involved in spermatozoa maturation and function. Ejaculated spermatozoa are still able to capture exosomes; exosomes of NSP individuals improve sperm motility and prompt capacitation, while exosomes of SA men fail to exert similar features.
STUDY DESIGN, SIZE, DURATION: Semen samples from NSP and SA men, aged 18 to 55 and registered at a single IVF center, were considered for this study project. Subjects were subdivided into three groups: a discovery cohort (five NSP men and six SA patients), a validation cohort (seven NSP and seven SA men) and the 'glycodelin analysis' cohort (20 NSP and 37 SA men). Exosomes were purified from semen of every participant.
PARTICIPANTS/MATERIALS, SETTING, METHODS: Exosomes were characterized by nanoparticle tracking analysis, transmission electron microscopy and western blot. Comprehensive proteomics analysis of the exosomal proteome was performed by nanoscale liquid chromatographic tandem mass spectrometry analysis. Funrich software was used to determine statistical enrichment of pathways, networks and Gene Ontology terms of the identified proteins. Validation of differentially expressed proteins was performed through ELISA and western blot analysis.
The comprehensive proteomic analysis identified a total of 2138 proteins for both groups. There were 89 proteins found to be differentially expressed in exosomes of NSP versus SA subjects, of which 37 were increased in the NSP group and 52 were increased in the SA group. One-third of the exosomes-associated proteins highly expressed in NSP samples were involved in the reproductive process; conversely, the over-expressed proteins in exosomes of SA samples were not functionally specific. Quantitative data were confirmed on seminal exosomes from different cohorts of subjects.
N/A.
LIMITATIONS, REASONS FOR CAUTION: Transfer of the proteins from exosomes to spermatozoa has been only partially demonstrated and up-take mechanisms are still poorly defined.
Seminal exosomes carry proteins that are potentially able to either favour or inhibit the reproductive process in humans. A better understanding of these phenomena might pave the way for novel intervention measures in terms of male infertility.
STUDY FUNDING/COMPETING INTEREST(S): This study was funded by the Italian Ministry of Health through an Institution Seed Grant. None of the authors has any competing interests.
正常精子(NSP)和严重弱精子(SA)男性精液中分离的外泌体的蛋白质组特征是否存在差异,这些差异可能与精子特征有关?
在 NSP 男性的精液外泌体中,一组已知的能正向调节精子功能的相关蛋白被过度表达,即富含半胱氨酸的分泌蛋白 1(CRISP1),而抑制蛋白糖蛋白 11 在 SA 受试者的外泌体中被富集。
外泌体是沿着男性生殖道分泌的,被认为参与精子的成熟和功能。射出的精子仍然能够捕获外泌体;NSP 个体的外泌体可改善精子运动能力并促使获能,而 SA 男性的外泌体则不能发挥类似的作用。
研究设计、规模、持续时间:本研究项目考虑了来自年龄在 18 至 55 岁之间的 NSP 和 SA 男性的精液样本,这些男性均在一个 IVF 中心注册。受试者被分为三组:一个发现队列(五名 NSP 男性和六名 SA 患者)、一个验证队列(七名 NSP 和七名 SA 男性)和“糖蛋白 11 分析”队列(20 名 NSP 和 37 名 SA 男性)。从每个参与者的精液中纯化外泌体。
参与者/材料、设置、方法:通过纳米颗粒跟踪分析、透射电子显微镜和 Western blot 对外泌体进行了表征。通过纳升液相色谱串联质谱分析对外泌体的蛋白质组进行了全面的蛋白质组学分析。使用 Funrich 软件确定了鉴定蛋白的通路、网络和基因本体论术语的统计富集。通过 ELISA 和 Western blot 分析验证差异表达蛋白。
综合蛋白质组学分析鉴定了两组共 2138 种蛋白质。在 NSP 与 SA 受试者的外泌体中发现了 89 种差异表达的蛋白质,其中 37 种在 NSP 组中增加,52 种在 SA 组中增加。在 NSP 样本中高度表达的三分之一外泌体相关蛋白参与生殖过程;相反,在 SA 样本中外泌体中过度表达的蛋白没有特定的功能。从不同队列的受试者的精液外泌体中证实了定量数据。
无。
局限性、谨慎的原因:蛋白质从外泌体转移到精子的过程仅部分得到证实,并且摄取机制仍未得到很好的定义。
精液外泌体携带的蛋白质可能有利于或抑制人类的生殖过程。对这些现象的更好理解可能为男性不育症的新干预措施铺平道路。
研究资金/利益冲突:本研究由意大利卫生部通过机构种子基金资助。作者均无任何利益冲突。