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Precipitation-based extracellular vesicle isolation from rat plasma co-precipitate vesicle-free microRNAs

机译:大鼠血浆共沉淀出囊泡免疫沉淀的沉淀基细胞外囊泡分离

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摘要

The microRNA (miRNA) cargo contained in plasma extracellular vesicles (EVs) offers a relatively little explored source of biomarkers for brain diseases that can be obtained noninvasively. Methods to isolate EVs from plasma, however, are still being developed. For EV isolation, it is important to ensure the removal of vesicle-free miRNAs, which account for approximately two-thirds of plasma miRNAs. Membrane particle precipitation-based EV isolation is an appealing method because of the simple protocol and high yield. Here, we evaluated the performance of a precipitation-based method to obtain enriched EV-specific miRNAs from a small volume of rat plasma. We performed size-exclusion chromatography (SEC) on precipitation-isolated EV pellets and whole plasma. The SEC fractions were analysed using Nanoparticle Tracking Analysis (NTA), protein and miRNA concentration assays, and droplet digital polymerase chain reaction for four miRNAs (miR-142-3p, miR-124-3p, miR-23a, miR-122). Precipitation-isolated EVs and selected SEC fractions from the plasma were also analysed with transmission electron microscopy (TEM). Precipitation-based EV isolation co-precipitated 9% to 15% of plasma proteins and 21% to 99% of vesicle-free miRNAs, depending on the individual miRNAs. In addition, the amount of miR-142-3p, found mainly in EV fractions, was decreased in the EV fractions, indicating that part of it was lost during precipitation-based isolation. Western blot and TEM revealed both protein and lipoprotein contamination in the precipitation-isolated EV-pellets. Our findings indicate that a precipitation-based method is not sufficient for purifying plasma EV-contained miRNA cargo. The particle number measured by NTA is high, but this is mostly due to the contaminating lipoproteins. Although a part of the vesicle-free miRNA is removed, vesicle-free miRNA still dominates in plasma EV pellets isolated by the precipitation-based method.
机译:的微小RNA(miRNA)的货物在血浆细胞外囊泡(EV)用的优惠含有相对小的探索,可以非侵入性地获得用于脑疾病的生物标志物的来源。方法从血浆中分离电动汽车,但仍在发展。对于EV的隔离,这是重要的,以确保除去游离囊泡的miRNA,占血浆miRNA的大约三分之二的。基于膜的沉淀粒子EV隔离是因为简单的协议和高产率的有吸引力的方法。在这里,我们评估了基于沉淀方法的性能,从大鼠血浆的小体积获得富集的EV-特异性miRNA。我们对沉淀分离EV粒料和全血浆进行大小排阻层析(SEC)。使用纳米粒子追踪分析(NTA)的SEC级分进行分析,蛋白质和miRNA浓度测定和四倍的miRNA(MIR-142-3p的,的miR-124-3p,的miR-23a中,的miR-122)的液滴数字聚合酶链反应。沉淀隔离EV和来自等离子体选择SEC级分进行了分析用透射电子显微镜(TEM)。沉淀基于EV隔离共沉淀取决于单个miRNA 9%至15%的血浆蛋白的21%至99%的自由囊泡miRNA的。此外,的miR-142-3p的量,主要存在于EV馏分,在EV级分减少,表明它的一部分期间,基于沉淀隔离丢失。 Western blot和TEM显示,在沉淀分离的EV-丸蛋白和脂蛋白污染。我们的研究结果表明,基于沉淀法是不够的等离子净化EV-miRNA的载货物。通过NTA测得的粒子数是高的,但是这主要是由于污染性脂蛋白。虽然自由囊泡-miRNA的一部分被移除,自由囊泡的miRNA仍然占主导地位在由基于沉淀法分离血浆EV粒料。

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