Department of Microsystems Engineering, Rochester Institute of Technology, Rochester, NY, United States; Department of Biomedical Engineering, Rochester Institute of Technology, Rochester, NY, United States.
Department of Microsystems Engineering, Rochester Institute of Technology, Rochester, NY, United States; Department of Biomedical Engineering, Rochester Institute of Technology, Rochester, NY, United States.
Methods Enzymol. 2020;645:15-42. doi: 10.1016/bs.mie.2020.09.002. Epub 2020 Sep 29.
Fluorescent labeling of extracellular vesicles (EVs) enables studying their uptake and influence on individual cells, biodistribution as well as facilitates their characterization using high-resolution flow cytometry at a single EV level. Here we describe the importance of fluorescent labeling, the available fluorescent dyes and labeling approaches, the characteristics of an ideal dye, and the available techniques for post-labeling purification. We discuss the importance of preserving the size of EVs for uptake, biodistribution, and characterization studies and focus on the effect of common lipophilic PKH and luminal CFSE dyes on the size of EVs. Lastly, we present an example protocol for luminal labeling of EVs and characterization of the effect of labeling on the size of EVs using nanoparticles tracking analysis (NTA).
细胞外囊泡 (EVs) 的荧光标记使研究它们的摄取和对单个细胞的影响、生物分布以及使用高分辨率流式细胞术在单个 EV 水平上对其进行表征成为可能。在这里,我们描述了荧光标记的重要性、可用的荧光染料和标记方法、理想染料的特性以及标记后纯化的可用技术。我们讨论了保持 EVs 的大小对于摄取、生物分布和表征研究的重要性,并重点关注常见亲脂性 PKH 和腔 CFSE 染料对 EVs 大小的影响。最后,我们提供了一个使用纳米颗粒跟踪分析 (NTA) 对 EVs 进行内腔标记和表征标记对 EVs 大小影响的示例方案。