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The impact of disparate isolation methods for extracellular vesicles on downstream RNA profiling

机译:细胞外囊泡的不同分离方法对下游RNA谱分析的影响

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摘要

Despite an enormous interest in the role of extracellular vesicles, including exosomes, in cancer and their use as biomarkers for diagnosis, prognosis, drug response and recurrence, there is no consensus on dependable isolation protocols. We provide a comparative evaluation of 4 exosome isolation protocols for their usability, yield and purity, and their impact on downstream omics approaches for biomarker discovery. OptiPrep density gradient centrifugation outperforms ultracentrifugation and ExoQuick and Total Exosome Isolation precipitation in terms of purity, as illustrated by the highest number of CD63-positive nanovesicles, the highest enrichment in exosomal marker proteins and a lack of contaminating proteins such as extracellular Argonaute-2 complexes. The purest exosome fractions reveal a unique mRNA profile enriched for translation, ribosome, mitochondrion and nuclear lumen function. Our results demonstrate that implementation of high purification techniques is a prerequisite to obtain reliable omics data and identify exosome-specific functions and biomarkers.
机译:尽管人们对包括外来体在内的细胞外囊泡在癌症中的作用及其作为诊断,预后,药物反应和复发的生物标志物的用途引起了极大的兴趣,但在可靠的分离方案上尚未达成共识。我们提供了4种外泌体分离方案的可用性,产量和纯度,以及它们对下游组学方法进行生物标记物发现的影响的比较评估。就纯度而言,OptiPrep密度梯度离心优于超速离心和ExoQuick和总外泌体分离沉淀,如CD63阳性纳米囊泡的数量最多,胞外标记蛋白的富集程度最高以及缺乏污染蛋白(例如细胞外Argonaute-2复合物) 。最纯净的外泌体部分显示出独特的mRNA谱,其丰富了翻译,核糖体,线粒体和核内腔功能。我们的结果表明,高纯度技术的实施是获得可靠的组学数据并鉴定外泌体特异性功能和生物标志物的前提。

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