Emily Sarah Jane Paterson, Simon Scheck, Simon McDowell, Nick Bedford, Jane Eleanor Girling, Claire Elizabeth Henry
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Isolated EVs were characterised through negative stain transmission electron microscopy (TEM), Western blotting (TSG101, CD63, Calnexin, ApoB, Albumin), tunable resistive pulse sensing (TRPS), microBCA assays and RT-qPCR of miRNAs. PCR was performed on samples prior to EV isolation to assess bacteria present in samples. Cervical brush and vaginal swab EVs were intact vesicles with limited co-isolated contaminants. Cervical brushes had higher concentrations of particles compared to match vaginal swabs, although both samples had low concentrations. Protein and miRNA yield were similar between matched samples. PCR demonstrated only a small amount DNA within samples was bacterial (>0.5%). Cervico-vaginal fluids EVs were successfully isolated from cervical brushes and vaginal swabs, demonstrating a new method of sampling reproductive EVs. EV yield from both sample types was low. 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引用次数: 0
摘要
子宫内膜异位症是一种常见的妇科疾病,诊断延迟时间较长。确诊需要手术,因此需要一种非侵入性的生物标志物。细胞外囊泡(EV)可能在子宫内膜异位症的发病机制中发挥作用,但目前有关EV生物标志物的文献十分有限。本研究旨在探讨使用宫颈刷和阴道拭子分离宫颈阴道液EV的可行性,并对这两种方法进行比较。在征得知情同意后,接受疑似子宫内膜异位症手术的患者在全身麻醉的情况下采集了宫颈刷和阴道拭子样本。通过阴性染色透射电子显微镜(TEM)、Western 印迹(TSG101、CD63、Calnexin、ApoB、Albumin)、可调电阻脉冲传感(TRPS)、microBCA 检测和 miRNA 的 RT-qPCR 对分离的 EVs 进行表征。在 EV 分离前对样本进行 PCR,以评估样本中存在的细菌。宫颈刷和阴道拭子的 EV 是完整的囊泡,共分离污染物有限。与匹配的阴道拭子相比,宫颈刷的颗粒浓度更高,尽管两种样本的浓度都很低。匹配样本的蛋白质和 miRNA 产量相似。聚合酶链式反应(PCR)显示,样本中只有少量 DNA 是细菌(0.5%)。宫颈阴道液 EVs 成功地从宫颈刷和阴道拭子中分离出来,展示了一种新的生殖 EVs 采样方法。两种样本的EV产量都很低。相似的蛋白质和 miRNA 水平表明,这两种取样方法都适用于生物标记物研究。
Comparison of cervicovaginal fluid extracellular vesicles isolated from paired cervical brushes and vaginal swabs
Endometriosis is a common gynaecological condition, with a long diagnostic delay. Surgery is required to confirm a diagnosis, highlighting the need for a non-invasive biomarker. Extracellular vesicles (EVs) may have a role in endometriosis pathogenesis, yet there is limited EV biomarker literature available. This study aimed to investigate the feasibility of isolating cervico-vaginal fluid EVs sampled using cervical brushes and vaginal swabs and to compare these methods. After providing informed consent, patients undergoing surgery for suspected endometriosis had cervical brush and vaginal swab samples collected under general anaesthetic. Isolated EVs were characterised through negative stain transmission electron microscopy (TEM), Western blotting (TSG101, CD63, Calnexin, ApoB, Albumin), tunable resistive pulse sensing (TRPS), microBCA assays and RT-qPCR of miRNAs. PCR was performed on samples prior to EV isolation to assess bacteria present in samples. Cervical brush and vaginal swab EVs were intact vesicles with limited co-isolated contaminants. Cervical brushes had higher concentrations of particles compared to match vaginal swabs, although both samples had low concentrations. Protein and miRNA yield were similar between matched samples. PCR demonstrated only a small amount DNA within samples was bacterial (>0.5%). Cervico-vaginal fluids EVs were successfully isolated from cervical brushes and vaginal swabs, demonstrating a new method of sampling reproductive EVs. EV yield from both sample types was low. Similar protein and miRNA levels suggest either sampling method may be suitable for biomarker studies.