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Evaluation of serum extracellular vesicle isolation methods for profiling miRNAs by next-generation sequencing

Extracellular vesicles (EVs) are intercellular communicators with key functions in physiological and pathological processes and have recently garnered interest because of their diagnostic and therapeutic potential. The past decade has brought about the development and commercialization of a wide arr...

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Autores principales: Buschmann, Dominik, Kirchner, Benedikt, Hermann, Stefanie, Märte, Melanie, Wurmser, Christine, Brandes, Florian, Kotschote, Stefan, Bonin, Michael, Steinlein, Ortrud K., Pfaffl, Michael W., Schelling, Gustav, Reithmair, Marlene
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5990937/
https://www.ncbi.nlm.nih.gov/pubmed/29887978
http://dx.doi.org/10.1080/20013078.2018.1481321
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author Buschmann, Dominik
Kirchner, Benedikt
Hermann, Stefanie
Märte, Melanie
Wurmser, Christine
Brandes, Florian
Kotschote, Stefan
Bonin, Michael
Steinlein, Ortrud K.
Pfaffl, Michael W.
Schelling, Gustav
Reithmair, Marlene
author_facet Buschmann, Dominik
Kirchner, Benedikt
Hermann, Stefanie
Märte, Melanie
Wurmser, Christine
Brandes, Florian
Kotschote, Stefan
Bonin, Michael
Steinlein, Ortrud K.
Pfaffl, Michael W.
Schelling, Gustav
Reithmair, Marlene
author_sort Buschmann, Dominik
collection PubMed
description Extracellular vesicles (EVs) are intercellular communicators with key functions in physiological and pathological processes and have recently garnered interest because of their diagnostic and therapeutic potential. The past decade has brought about the development and commercialization of a wide array of methods to isolate EVs from serum. Which subpopulations of EVs are captured strongly depends on the isolation method, which in turn determines how suitable resulting samples are for various downstream applications. To help clinicians and scientists choose the most appropriate approach for their experiments, isolation methods need to be comparatively characterized. Few attempts have been made to comprehensively analyse vesicular microRNAs (miRNAs) in patient biofluids for biomarker studies. To address this discrepancy, we set out to benchmark the performance of several isolation principles for serum EVs in healthy individuals and critically ill patients. Here, we compared five different methods of EV isolation in combination with two RNA extraction methods regarding their suitability for biomarker discovery-focused miRNA sequencing as well as biological characteristics of captured vesicles. Our findings reveal striking method-specific differences in both the properties of isolated vesicles and the ability of associated miRNAs to serve in biomarker research. While isolation by precipitation and membrane affinity was highly suitable for miRNA-based biomarker discovery, methods based on size-exclusion chromatography failed to separate patients from healthy volunteers. Isolated vesicles differed in size, quantity, purity and composition, indicating that each method captured distinctive populations of EVs as well as additional contaminants. Even though the focus of this work was on transcriptomic profiling of EV-miRNAs, our insights also apply to additional areas of research. We provide guidance for navigating the multitude of EV isolation methods available today and help researchers and clinicians make an informed choice about which strategy to use for experiments involving critically ill patients.
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spelling pubmed-59909372018-06-08 Evaluation of serum extracellular vesicle isolation methods for profiling miRNAs by next-generation sequencing Buschmann, Dominik Kirchner, Benedikt Hermann, Stefanie Märte, Melanie Wurmser, Christine Brandes, Florian Kotschote, Stefan Bonin, Michael Steinlein, Ortrud K. Pfaffl, Michael W. Schelling, Gustav Reithmair, Marlene J Extracell Vesicles Research Article Extracellular vesicles (EVs) are intercellular communicators with key functions in physiological and pathological processes and have recently garnered interest because of their diagnostic and therapeutic potential. The past decade has brought about the development and commercialization of a wide array of methods to isolate EVs from serum. Which subpopulations of EVs are captured strongly depends on the isolation method, which in turn determines how suitable resulting samples are for various downstream applications. To help clinicians and scientists choose the most appropriate approach for their experiments, isolation methods need to be comparatively characterized. Few attempts have been made to comprehensively analyse vesicular microRNAs (miRNAs) in patient biofluids for biomarker studies. To address this discrepancy, we set out to benchmark the performance of several isolation principles for serum EVs in healthy individuals and critically ill patients. Here, we compared five different methods of EV isolation in combination with two RNA extraction methods regarding their suitability for biomarker discovery-focused miRNA sequencing as well as biological characteristics of captured vesicles. Our findings reveal striking method-specific differences in both the properties of isolated vesicles and the ability of associated miRNAs to serve in biomarker research. While isolation by precipitation and membrane affinity was highly suitable for miRNA-based biomarker discovery, methods based on size-exclusion chromatography failed to separate patients from healthy volunteers. Isolated vesicles differed in size, quantity, purity and composition, indicating that each method captured distinctive populations of EVs as well as additional contaminants. Even though the focus of this work was on transcriptomic profiling of EV-miRNAs, our insights also apply to additional areas of research. We provide guidance for navigating the multitude of EV isolation methods available today and help researchers and clinicians make an informed choice about which strategy to use for experiments involving critically ill patients. Taylor & Francis 2018-06-04 /pmc/articles/PMC5990937/ /pubmed/29887978 http://dx.doi.org/10.1080/20013078.2018.1481321 Text en © 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group on behalf of The International Society for Extracellular Vesicles. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Buschmann, Dominik
Kirchner, Benedikt
Hermann, Stefanie
Märte, Melanie
Wurmser, Christine
Brandes, Florian
Kotschote, Stefan
Bonin, Michael
Steinlein, Ortrud K.
Pfaffl, Michael W.
Schelling, Gustav
Reithmair, Marlene
Evaluation of serum extracellular vesicle isolation methods for profiling miRNAs by next-generation sequencing
title Evaluation of serum extracellular vesicle isolation methods for profiling miRNAs by next-generation sequencing
title_full Evaluation of serum extracellular vesicle isolation methods for profiling miRNAs by next-generation sequencing
title_fullStr Evaluation of serum extracellular vesicle isolation methods for profiling miRNAs by next-generation sequencing
title_full_unstemmed Evaluation of serum extracellular vesicle isolation methods for profiling miRNAs by next-generation sequencing
title_short Evaluation of serum extracellular vesicle isolation methods for profiling miRNAs by next-generation sequencing
title_sort evaluation of serum extracellular vesicle isolation methods for profiling mirnas by next-generation sequencing
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5990937/
https://www.ncbi.nlm.nih.gov/pubmed/29887978
http://dx.doi.org/10.1080/20013078.2018.1481321
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