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A Simplified Method to Recover Urinary Vesicles for Clinical Applications, and Sample Banking

Urinary extracellular vesicles provide a novel source for valuable biomarkers for kidney and urogenital diseases: Current isolation protocols include laborious, sequential centrifugation steps which hampers their widespread research and clinical use. Furthermore, large individual urine sample volume...

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Autores principales: Musante, Luca, Tataruch, Dorota, Gu, Dongfeng, Benito-Martin, Alberto, Calzaferri, Giulio, Aherne, Sinead, Holthofer, Harry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4274508/
https://www.ncbi.nlm.nih.gov/pubmed/25532487
http://dx.doi.org/10.1038/srep07532
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author Musante, Luca
Tataruch, Dorota
Gu, Dongfeng
Benito-Martin, Alberto
Calzaferri, Giulio
Aherne, Sinead
Holthofer, Harry
author_facet Musante, Luca
Tataruch, Dorota
Gu, Dongfeng
Benito-Martin, Alberto
Calzaferri, Giulio
Aherne, Sinead
Holthofer, Harry
author_sort Musante, Luca
collection PubMed
description Urinary extracellular vesicles provide a novel source for valuable biomarkers for kidney and urogenital diseases: Current isolation protocols include laborious, sequential centrifugation steps which hampers their widespread research and clinical use. Furthermore, large individual urine sample volumes or sizable target cohorts are to be processed (e.g. for biobanking), the storage capacity is an additional problem. Thus, alternative methods are necessary to overcome such limitations. We have developed a practical vesicle isolation technique to yield easily manageable sample volumes in an exceptionally cost efficient way to facilitate their full utilization in less privileged environments and maximize the benefit of biobanking. Urinary vesicles were isolated by hydrostatic dialysis with minimal interference of soluble proteins or vesicle loss. Large volumes of urine were concentrated up to 1/100 of original volume and the dialysis step allowed equalization of urine physico-chemical characteristics. Vesicle fractions were found suitable to any applications, including RNA analysis. In the yield, our hydrostatic filtration dialysis system outperforms the conventional ultracentrifugation-based methods and the labour intensive and potentially hazardous step of ultracentrifugations are eliminated. Likewise, the need for trained laboratory personnel and heavy initial investment is avoided. Thus, our method qualifies as a method for laboratories working with urinary vesicles and biobanking.
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spelling pubmed-42745082014-12-29 A Simplified Method to Recover Urinary Vesicles for Clinical Applications, and Sample Banking Musante, Luca Tataruch, Dorota Gu, Dongfeng Benito-Martin, Alberto Calzaferri, Giulio Aherne, Sinead Holthofer, Harry Sci Rep Article Urinary extracellular vesicles provide a novel source for valuable biomarkers for kidney and urogenital diseases: Current isolation protocols include laborious, sequential centrifugation steps which hampers their widespread research and clinical use. Furthermore, large individual urine sample volumes or sizable target cohorts are to be processed (e.g. for biobanking), the storage capacity is an additional problem. Thus, alternative methods are necessary to overcome such limitations. We have developed a practical vesicle isolation technique to yield easily manageable sample volumes in an exceptionally cost efficient way to facilitate their full utilization in less privileged environments and maximize the benefit of biobanking. Urinary vesicles were isolated by hydrostatic dialysis with minimal interference of soluble proteins or vesicle loss. Large volumes of urine were concentrated up to 1/100 of original volume and the dialysis step allowed equalization of urine physico-chemical characteristics. Vesicle fractions were found suitable to any applications, including RNA analysis. In the yield, our hydrostatic filtration dialysis system outperforms the conventional ultracentrifugation-based methods and the labour intensive and potentially hazardous step of ultracentrifugations are eliminated. Likewise, the need for trained laboratory personnel and heavy initial investment is avoided. Thus, our method qualifies as a method for laboratories working with urinary vesicles and biobanking. Nature Publishing Group 2014-12-23 /pmc/articles/PMC4274508/ /pubmed/25532487 http://dx.doi.org/10.1038/srep07532 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Article
Musante, Luca
Tataruch, Dorota
Gu, Dongfeng
Benito-Martin, Alberto
Calzaferri, Giulio
Aherne, Sinead
Holthofer, Harry
A Simplified Method to Recover Urinary Vesicles for Clinical Applications, and Sample Banking
title A Simplified Method to Recover Urinary Vesicles for Clinical Applications, and Sample Banking
title_full A Simplified Method to Recover Urinary Vesicles for Clinical Applications, and Sample Banking
title_fullStr A Simplified Method to Recover Urinary Vesicles for Clinical Applications, and Sample Banking
title_full_unstemmed A Simplified Method to Recover Urinary Vesicles for Clinical Applications, and Sample Banking
title_short A Simplified Method to Recover Urinary Vesicles for Clinical Applications, and Sample Banking
title_sort simplified method to recover urinary vesicles for clinical applications, and sample banking
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4274508/
https://www.ncbi.nlm.nih.gov/pubmed/25532487
http://dx.doi.org/10.1038/srep07532
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