Division of Epidemiology, Department of Environmental Health, University of Cincinnati College of Medicine, Cincinnati, OH, United States of America.
Cincinnati Cancer Center, Cincinnati, OH, United States of America.
PLoS One. 2020 Apr 10;15(4):e0229976. doi: 10.1371/journal.pone.0229976. eCollection 2020.
Small extracellular vesicles (sEV) are nano-sized (40-150 nm), membrane-encapsulated vesicles that are released by essentially all cells into the extracellular space and function as intercellular signaling vectors through the horizontal transfer of biologic molecules, including microRNA (miRNA) and other small non-coding RNA (ncRNA), that can alter the phenotype of recipient cells. sEV are present in essentially all extracellular biofluids, including serum, urine and saliva, and offer a new avenue for discovery and development of novel biomarkers of various disease states and exposures. The objective of this study was to systematically interrogate similarities and differences between sEV ncRNA derived from saliva, serum and urine, as well as cell-free small ncRNA (cf-ncRNA) from serum. Saliva, urine and serum were concomitantly collected from 4 healthy donors to mitigate potential bias that can stem from interpersonal and temporal variability. sEV were isolated from each respective biofluid, along with cf-RNA from serum. sEV were isolated from the respective biofluids via differential ultracentrifugation with a 30% sucrose cushion to minimize protein contamination. Small RNA-sequencing was performed on each sample, and cluster analysis was performed based on ncRNA profiles. While some similarities existed in terms of sEV ncRNA cargo across biofluids, there are also notable differences in ncRNA class and ncRNA secretion, with sEV in each biofluid bearing a unique ncRNA profile, including major differences in composition by ncRNA class. We conclude that sEV ncRNA cargo varies according to biofluid, so thus should be carefully selected and interpreted when designing or contrasting translational or epidemiological studies.
小细胞外囊泡 (sEV) 是纳米大小的 (40-150nm),膜包裹的囊泡,基本上所有细胞都会将其释放到细胞外空间,通过生物分子的水平转移作为细胞间信号载体,包括 microRNA (miRNA) 和其他小非编码 RNA (ncRNA),这些分子可以改变受体细胞的表型。sEV 存在于基本上所有的细胞外生物流体中,包括血清、尿液和唾液,并为发现和开发各种疾病状态和暴露的新型生物标志物提供了新途径。本研究的目的是系统地研究来自唾液、血清和尿液的 sEV ncRNA 以及来自血清的无细胞小 ncRNA (cf-ncRNA) 之间的相似性和差异。从 4 位健康供体中同时采集唾液、尿液和血清,以减轻可能源于人与人之间和时间变化的潜在偏差。从每个相应的生物流体中分离 sEV,并从血清中分离 cf-RNA。通过在 30%蔗糖垫上进行差速超速离心,从相应的生物流体中分离 sEV,以最大程度地减少蛋白质污染。对每个样本进行小 RNA 测序,并根据 ncRNA 图谱进行聚类分析。虽然在生物流体之间存在一些关于 sEV ncRNA 货物的相似性,但 ncRNA 类和 ncRNA 分泌也存在显著差异,每个生物流体中的 sEV 具有独特的 ncRNA 图谱,包括 ncRNA 类组成的主要差异。我们得出结论,sEV ncRNA 货物根据生物流体而变化,因此在设计或对比转化或流行病学研究时,应仔细选择和解释。