García-Arauzo Marta, Reymond Sandrine, Gruaz Lyssia, Schvartz Domitille, Civic Natacha, Docquier Mylène, Deffert Christine, Colosetti Pascal, Sanchez Jean-Charles, Bridel Claire
Translational Biomarker Group, Department of Medicine, Faculty of Medicine University of Geneva Geneva Switzerland.
Proteomics Core Facility, Faculty of Medicine University of Geneva Geneva Switzerland.
J Extracell Biol. 2025 Aug 11;4(8):e70076. doi: 10.1002/jex2.70076. eCollection 2025 Aug.
Proteomic and transcriptomic analyses of cerebrospinal fluid (CSF)-derived extracellular vesicles (EVs) offer unique insights into molecular changes associated with central nervous system (CNS) diseases and may result in biomarker identification. No gold standard method to enrich EVs from CSF has been established, and head-to-head comparisons of outputs of different protocols are scarce. Using a large pool of CSF, we characterised the EV preparations resulting from four enrichment protocols and compared them in terms of yield and purity. We found that particles enriched by ultracentrifugation (UC) or a combination of ultrafiltration and size exclusion chromatography (UF-SEC) exhibited the typical morphological and biochemical characteristics of small EVs and were highly enriched in proteins and polyadenylated (polyA) transcripts associated with EV-related biological processes. UF-SEC preparations had higher particle yields, whilst more proteins were identified in UC preparations. Approximately 40% of the EV preparations' proteome was not identified in unenriched CSF, among which a core proteome of 45 proteins was identified in 30 EV preparations from independent experiments, which may serve as CSF-derived EV markers. Enrichment scores to protein contaminants, albumin and apolipoprotein E were higher in UF-SEC preparations. In conclusion, all protocols analysed here resulted in enrichment of particles with small EV characteristics, with EV enrichments from UF-SEC resulting in the highest yield and purity.
对脑脊液(CSF)来源的细胞外囊泡(EVs)进行蛋白质组学和转录组学分析,能为与中枢神经系统(CNS)疾病相关的分子变化提供独特见解,并可能有助于识别生物标志物。目前尚未建立从脑脊液中富集细胞外囊泡的金标准方法,不同方案产出的直接比较也很少见。我们使用大量脑脊液,对四种富集方案得到的细胞外囊泡制剂进行了表征,并在产量和纯度方面进行了比较。我们发现,通过超速离心(UC)或超滤与尺寸排阻色谱联用(UF-SEC)富集的颗粒呈现出小细胞外囊泡典型的形态和生化特征,并且高度富集了与细胞外囊泡相关生物过程的蛋白质和聚腺苷酸化(polyA)转录本。UF-SEC制剂的颗粒产量更高,而在UC制剂中鉴定出的蛋白质更多。在未富集的脑脊液中未鉴定出约40%的细胞外囊泡制剂蛋白质组,其中在独立实验的30个细胞外囊泡制剂中鉴定出了一个由45种蛋白质组成的核心蛋白质组,其可能作为脑脊液来源的细胞外囊泡标志物。UF-SEC制剂中对蛋白质污染物、白蛋白和载脂蛋白E的富集分数更高。总之,这里分析的所有方案都能富集具有小细胞外囊泡特征的颗粒,其中UF-SEC的细胞外囊泡富集物产量最高、纯度最高。