Arakelyan Anush, Ivanova Oxana, Vasilieva Elena, Grivel Jean-Charles, Margolis Leonid
Program in Physical Biology, Eunice Kennedy-Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD, USA.
Atherothrombosis Department, Moscow State University of Medicine and Dentistry, Moscow, Russia.
Nanomedicine. 2015 Apr;11(3):489-98. doi: 10.1016/j.nano.2014.09.020. Epub 2014 Dec 3.
Extracellular vesicles (EVs) are important in normal physiology and are altered in various pathologies. EVs produced by different cells are antigenically different. Since the majority of EVs are too small for routine flow cytometry, EV composition is studied predominantly in bulk, thus not addressing their antigenic heterogeneity. Here, we describe a nanoparticle-based technique for analyzing antigens on single nano-sized EVs. The technique consists of immuno-capturing of EVs with 15-nm magnetic nanoparticles, staining captured EVs with antibodies against their antigens, and separating them from unbound EVs and free antibodies in a magnetic field, followed by flow analysis. This technique allows us to characterize EVs populations according to their antigenic distribution, including minor EV fractions. We demonstrated that the individual blood EVs carry different sets of antigens, none being ubiquitous, and quantified their distribution. The physiological significance of antigenically different EVs and their correlation with different pathologies can now be directly addressed. From the clinical editor: This study reports a nanoparticle-based technique for analyzing antigens on single nano-sized extracellular vehicles (EV). The technique consists of immuno-capturing of EVs with 15-nm magnetic nanoparticles, followed by staining the captured EVs with antibodies and separating them via a magnetic field, followed by flow analysis. This technique enables studies of antigenic properties of individual EVs that conventionally can only be studied in bulk.
细胞外囊泡(EVs)在正常生理过程中发挥着重要作用,且在多种病理状态下会发生改变。不同细胞产生的EVs在抗原性上存在差异。由于大多数EVs体积过小,无法用常规流式细胞术进行检测,因此对EVs组成的研究主要是整体分析,并未考虑其抗原异质性。在此,我们描述了一种基于纳米颗粒的技术,用于分析单个纳米级EVs上的抗原。该技术包括用15纳米的磁性纳米颗粒免疫捕获EVs,用针对其抗原的抗体对捕获的EVs进行染色,并在磁场中将其与未结合的EVs和游离抗体分离,随后进行流式分析。这项技术使我们能够根据抗原分布来表征EVs群体,包括少量的EVs组分。我们证明了单个血液中的EVs携带不同的抗原组合,没有一种抗原是普遍存在的,并对其分布进行了量化。现在可以直接探讨抗原性不同的EVs的生理意义及其与不同病理状态的相关性。临床编辑评论:本研究报告了一种基于纳米颗粒的技术,用于分析单个纳米级细胞外囊泡(EV)上的抗原。该技术包括用15纳米的磁性纳米颗粒免疫捕获EVs,随后用抗体对捕获的EVs进行染色,并通过磁场将其分离,然后进行流式分析。这项技术能够研究单个EVs的抗原特性,而这些特性传统上只能进行整体研究。