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MIFlowCyt‐EV: a framework for standardized reporting of extracellular vesicle flow cytometry experiments

细胞外小泡 标准化 计算机科学 胞外囊泡 流式细胞术 灵敏度(控制系统) 度量(数据仓库) 领域(数学) 纳米技术 医学物理学 数据科学 数据挖掘 物理 医学 微泡 化学 材料科学 数学 免疫学 生物 工程类 纯数学 基因 小RNA 生物化学 电子工程 细胞生物学 操作系统
作者
Joshua A Welsh,Edwin van der Pol,Ger J. A. Arkesteijn,Michel Bremer,Alain Brisson,Frank A. W. Coumans,Françoise Dignat‐George,E. Duggan,Ionita Ghiran,Bernd Giebel,André Görgens,An Hendrix,Romaric Lacroix,Joanne Lannigan,Sten F.W.M. Libregts,Estefanía Lozano‐Andrés,Aizea Morales‐Kastresana,Stéphane Robert,Leonie de Rond,Tobias Tertel
出处
期刊:Journal of extracellular vesicles [Wiley]
卷期号:9 (1) 被引量:373
标识
DOI:10.1080/20013078.2020.1713526
摘要

ABSTRACT Extracellular vesicles (EVs) are small, heterogeneous and difficult to measure. Flow cytometry (FC) is a key technology for the measurement of individual particles, but its application to the analysis of EVs and other submicron particles has presented many challenges and has produced a number of controversial results, in part due to limitations of instrument detection, lack of robust methods and ambiguities in how data should be interpreted. These complications are exacerbated by the field's lack of a robust reporting framework, and many EV‐FC manuscripts include incomplete descriptions of methods and results, contain artefacts stemming from an insufficient instrument sensitivity and inappropriate experimental design and lack appropriate calibration and standardization. To address these issues, a working group (WG) of EV‐FC researchers from ISEV, ISAC and ISTH, worked together as an EV‐FC WG and developed a consensus framework for the minimum information that should be provided regarding EV‐FC. This framework incorporates the existing Minimum Information for Studies of EVs (MISEV) guidelines and Minimum Information about a FC experiment (MIFlowCyt) standard in an EV‐FC‐specific reporting framework (MIFlowCyt‐EV) that supports reporting of critical information related to sample staining, EV detection and measurement and experimental design in manuscripts that report EV‐FC data. MIFlowCyt‐EV provides a structure for sharing EV‐FC results, but it does not prescribe specific protocols, as there will continue to be rapid evolution of instruments and methods for the foreseeable future. MIFlowCyt‐EV accommodates this evolution, while providing information needed to evaluate and compare different approaches. Because MIFlowCyt‐EV will ensure consistency in the manner of reporting of EV‐FC studies, over time we expect that adoption of MIFlowCyt‐EV as a standard for reporting EV‐ FC studies will improve the ability to quantitatively compare results from different laboratories and to support the development of new instruments and assays for improved measurement of EVs.
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