Comparison of commercial exosome isolation kits for circulating exosomal microRNA profiling

被引:165
作者
Ding, Meng [1 ,2 ]
Wang, Cheng [1 ,2 ]
Lu, Xiaolan [1 ,2 ]
Zhang, Cuiping [1 ,2 ]
Zhou, Zhen [2 ]
Chen, Xi [2 ]
Zhang, Chen-Yu [2 ]
Zen, Ke [2 ]
Zhang, Chunni [1 ,2 ]
机构
[1] Nanjing Univ, Sch Life Sci, NAILS, Jinling Hosp,Dept Clin LabState Key Lab Analyt Ch, 305 East Zhongshan Rd, Nanjing 210002, Jiangsu, Peoples R China
[2] Nanjing Univ, Sch Life Sci, NAILS, Jiangsu Engn Res Ctr MicroRNA Biol & Biotechnol,S, 163 Xianlin Rd, Nanjing 210046, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Exosome; Exosomal miRNA; Commercial kits; Serum; Plasma; Comparison; BIOMARKERS; SERUM; VESICLES; PLASMA; MIRNAS; PROTOCOL;
D O I
10.1007/s00216-018-1052-4
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
Circulating exosomal microRNAs (miRNAs) are valuable biomarker candidates; however, information on the characterization and mutual agreement of commercial kits for circulating exosomal miRNA profiling is scarce. Here, we analyzed the advantages and weaknesses of four commonly used commercial kits for exosomal miRNA profiling and their application to the sample of serum and/or plasma, respectively. NanoSight and Western blotting were conducted to evaluate the efficiency and purity of the isolated exosomes. In our conditions, the size distribution of the isolated particles was appropriate (40-150 nm), and ExoQuick (TM) Exosome Precipitation Solution (EXQ) generated a relatively high yield of exosomes. Nevertheless, albumin impurity was ubiquitous for all the four kits, and Total Exosome Isolation for serum or plasma (TEI) yielded a relatively pure isolation. We further performed Illumina sequencing combined with RT-qPCR to determine the ability of these kits for miRNA profiling. There was significant correlation of the exosomal miRNA profile and specific miRNAs between kits, but with differences depending on methods. exoRNeasy Serum/Plasma Midi Kit (EXR) and EXQ performed better in the specific exosomal miRNAs recovery. Intraassay CVs for specific miRNA measurement were 0.88-3.82, 1.19-3.77, 0-2.70, and 1.23-9.11% for EXR, TEI, EXQ, and RIBO (TM) Exosome Isolation Reagent (REI), respectively. In each kit, serum yielded a higher abundance of exosomes and exosomal miRNAs than plasma, yet with more albumin impurity. In conclusion, our data provide some valuable guidance for the methodology of disease biomarker identification of circulation exosomal miRNAs.
引用
收藏
页码:3805 / 3814
页数:10
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