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细胞外囊泡研究中样本采集、分离和分析方法的标准化。

Standardization of sample collection, isolation and analysis methods in extracellular vesicle research.

机构信息

Department of Molecular and Comparative Pathobiology, Johns Hopkins University School of Medicine, MD, USA.

出版信息

J Extracell Vesicles. 2013 May 27;2. doi: 10.3402/jev.v2i0.20360. eCollection 2013.


DOI:10.3402/jev.v2i0.20360
PMID:24009894
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3760646/
Abstract

The emergence of publications on extracellular RNA (exRNA) and extracellular vesicles (EV) has highlighted the potential of these molecules and vehicles as biomarkers of disease and therapeutic targets. These findings have created a paradigm shift, most prominently in the field of oncology, prompting expanded interest in the field and dedication of funds for EV research. At the same time, understanding of EV subtypes, biogenesis, cargo and mechanisms of shuttling remains incomplete. The techniques that can be harnessed to address the many gaps in our current knowledge were the subject of a special workshop of the International Society for Extracellular Vesicles (ISEV) in New York City in October 2012. As part of the "ISEV Research Seminar: Analysis and Function of RNA in Extracellular Vesicles (evRNA)", 6 round-table discussions were held to provide an evidence-based framework for isolation and analysis of EV, purification and analysis of associated RNA molecules, and molecular engineering of EV for therapeutic intervention. This article arises from the discussion of EV isolation and analysis at that meeting. The conclusions of the round table are supplemented with a review of published materials and our experience. Controversies and outstanding questions are identified that may inform future research and funding priorities. While we emphasize the need for standardization of specimen handling, appropriate normative controls, and isolation and analysis techniques to facilitate comparison of results, we also recognize that continual development and evaluation of techniques will be necessary as new knowledge is amassed. On many points, consensus has not yet been achieved and must be built through the reporting of well-controlled experiments.

摘要

细胞外 RNA(exRNA)和细胞外囊泡(EV)相关出版物的出现突显了这些分子和载体作为疾病生物标志物和治疗靶点的潜力。这些发现引发了范式转变,在肿瘤学领域最为明显,促使人们对该领域产生了更大的兴趣,并为 EV 研究投入了资金。与此同时,对 EV 亚型、生物发生、货物和运输机制的理解仍不完整。可以利用哪些技术来解决我们目前知识中的许多空白点,是 2012 年 10 月在纽约市举行的国际细胞外囊泡学会(ISEV)特别研讨会的主题。作为“ISEV 研究研讨会:细胞外囊泡中 RNA 的分析和功能(evRNA)”的一部分,举行了 6 次圆桌讨论,为 EV 的分离和分析、相关 RNA 分子的纯化和分析以及 EV 的分子工程治疗干预提供了一个基于证据的框架。本文源于该会议上对 EV 分离和分析的讨论。圆桌会议的结论补充了对已发表材料和我们经验的回顾。确定了争议和悬而未决的问题,这些问题可能为未来的研究和资金重点提供信息。虽然我们强调需要标准化标本处理、适当的规范对照以及分离和分析技术,以促进结果比较,但我们也认识到,随着新知识的积累,需要不断开发和评估技术。在许多方面,尚未达成共识,必须通过报告精心控制的实验来建立共识。

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[10]
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本文引用的文献

[1]
International Society for Extracellular Vesicles: first annual meeting, April 17-21, 2012: ISEV-2012.

J Extracell Vesicles. 2012-12-28

[2]
ISEV RNA Workshop-New York City, October 1-2, 2012.

J Extracell Vesicles. 2012-10-19

[3]
EVpedia: an integrated database of high-throughput data for systemic analyses of extracellular vesicles.

J Extracell Vesicles. 2013-3-19

[4]
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J Extracell Vesicles. 2013-2-15

[5]
As we wait: coping with an imperfect nomenclature for extracellular vesicles.

J Extracell Vesicles. 2013-2-15

[6]
CD4(+) T cell activation promotes the differential release of distinct populations of nanosized vesicles.

J Extracell Vesicles. 2012-4-16

[7]
Characterization of mRNA and microRNA in human mast cell-derived exosomes and their transfer to other mast cells and blood CD34 progenitor cells.

J Extracell Vesicles. 2012-4-16

[8]
Diverse subpopulations of vesicles secreted by different intracellular mechanisms are present in exosome preparations obtained by differential ultracentrifugation.

J Extracell Vesicles. 2012-4-16

[9]
Standardization of pre-analytical variables in plasma microparticle determination: results of the International Society on Thrombosis and Haemostasis SSC Collaborative workshop.

J Thromb Haemost. 2013-4-2

[10]
Extracellular vesicles: exosomes, microvesicles, and friends.

J Cell Biol. 2013-2-18

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