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用于细胞外囊泡分离和表征的技术:一项全球调查结果

Techniques used for the isolation and characterization of extracellular vesicles: results of a worldwide survey.

作者信息

Gardiner Chris, Di Vizio Dolores, Sahoo Susmita, Théry Clotilde, Witwer Kenneth W, Wauben Marca, Hill Andrew F

机构信息

Haemostasis Research Unit, Research Department of Haematology, University College London, London, UK;

Icahn School of Medicine, Cardiovascular Research Center, Cedars-Sinai, Los Angeles, CA, USA.

出版信息

J Extracell Vesicles. 2016 Oct 31;5:32945. doi: 10.3402/jev.v5.32945. eCollection 2016.

Abstract

Extracellular vesicles (EVs) represent an important mode of intercellular communication. Research in this field has grown rapidly in the last few years, and there is a plethora of techniques for the isolation and characterization of EVs, many of which are poorly standardized. EVs are heterogeneous in size, origin and molecular constituents, with considerable overlap in size and phenotype between different populations of EVs. Little is known about current practices for the isolation, purification and characterization of EVs. We report here the first large, detailed survey of current worldwide practices for the isolation and characterization of EVs. Conditioned cell culture media was the most widely used material (83%). Ultracentrifugation remains the most commonly used isolation method (81%) with 59% of respondents use a combination of methods. Only 9% of respondents used only 1 characterization method, with others using 2 or more methods. Sample volume, sample type and downstream application all influenced the isolation and characterization techniques employed.

摘要

细胞外囊泡(EVs)是细胞间通讯的一种重要方式。在过去几年中,该领域的研究发展迅速,有大量用于分离和鉴定细胞外囊泡的技术,其中许多技术的标准化程度很低。细胞外囊泡在大小、来源和分子组成上具有异质性,不同群体的细胞外囊泡在大小和表型上有相当大的重叠。目前对于细胞外囊泡的分离、纯化和鉴定方法知之甚少。我们在此报告了第一项关于当前全球范围内细胞外囊泡分离和鉴定方法的大型详细调查。条件性细胞培养基是使用最广泛的材料(83%)。超速离心仍然是最常用的分离方法(81%),59%的受访者使用多种方法相结合。只有9%的受访者仅使用1种鉴定方法,其他受访者使用2种或更多方法。样本体积、样本类型和下游应用都会影响所采用的分离和鉴定技术。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/785e/5090131/d6568b410be8/JEV-5-32945-g001.jpg

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