Mørk Morten, Handberg Aase, Pedersen Shona, Jørgensen Malene M, Bæk Rikke, Nielsen Morten K, Kristensen Søren R
Department of Clinical Biochemistry, Aalborg University Hospital, Aalborg, Denmark.
AF Study Group, Aalborg University Hospital, Aalborg, Denmark.
J Extracell Vesicles. 2017 Apr 4;6(1):1308779. doi: 10.1080/20013078.2017.1308779. eCollection 2017.
: Nanoparticle tracking analysis (NTA) enables measurement of extracellular vesicles (EVs) but lacks the ability to distinct between EVs and lipoproteins which are abundantly present in blood plasma. Limitations in ultracentrifugation and size exclusion chromatography applied for EV isolation may result in inadequate EV purification and preservation. In this proof of concept study, we aimed to evaluate the potential of antibody-mediated removal of lipoproteins from plasma prior to extracellular vesicle (EV) analysis by nanoparticle tracking analysis (NTA). : Ten platelet-free plasma (PFP) samples from healthy fasting subjects were incubated with magnetic beads coated with antibodies against apolipoprotein B-48 and B-100 (ApoB). Plasma samples were analysed with NTA before and after application of the bead procedure. Four fasting PFP samples were analysed with an ELISA specific for human ApoB to estimate the degree of removal of lipoproteins and EV array analysis was used for identification of possible EV loss. : The magnetic bead separation procedure resulted in a median reduction of the particle concentration in plasma by 62% (interquartile range 32-72%). The mean size of the remaining particles generally increased. ApoB concentration was reduced to a level close to the background signal, whereas a median reduction of the EV content by 21% (range 8-43%) was observed. : Anti-ApoB antibody coated magnetic beads may hold potential for removal of lipoproteins from human PFP prior to EV measurement by NTA but some artefactual effect and EV loss may have to be endured.
纳米颗粒跟踪分析(NTA)能够测量细胞外囊泡(EV),但缺乏区分EV与血浆中大量存在的脂蛋白的能力。用于EV分离的超速离心和尺寸排阻色谱法存在局限性,可能导致EV纯化和保存不充分。在本概念验证研究中,我们旨在评估在通过纳米颗粒跟踪分析(NTA)进行细胞外囊泡(EV)分析之前,抗体介导从血浆中去除脂蛋白的潜力。:将来自健康空腹受试者的10份无血小板血浆(PFP)样本与包被有抗载脂蛋白B-48和B-100(ApoB)抗体的磁珠孵育。在应用磁珠程序前后,用NTA分析血浆样本。用针对人ApoB的ELISA分析4份空腹PFP样本,以估计脂蛋白的去除程度,并使用EV阵列分析来确定可能的EV损失。:磁珠分离程序使血浆中的颗粒浓度中位数降低了62%(四分位间距32 - 72%)。剩余颗粒的平均大小通常增加。ApoB浓度降低到接近背景信号的水平,而观察到EV含量中位数降低了21%(范围8 - 43%)。:包被抗ApoB抗体的磁珠在通过NTA测量EV之前,可能具有从人PFP中去除脂蛋白的潜力,但可能不得不承受一些人为效应和EV损失。