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Licensed Unlicensed Requires Authentication Published by De Gruyter October 5, 2013

Optimizing the purification and analysis of miRNAs from urinary exosomes

  • Sarath Kiran Channavajjhala , Marzia Rossato , Francesca Morandini , Annalisa Castagna , Francesca Pizzolo , Flavia Bazzoni and Oliviero Olivieri EMAIL logo

Abstract

Background: Exosomes are cytoplasm containing vesicles released by many cells that can be found in several biological fluids including urine. Urinary exosomes are released from every segment of the nephron, are detectable in urine, constitutively contain RNA (small RNAs and mRNAs) and harbor unique subset of proteins, reflecting their cellular source.

Methods: With the aim of establishing the optimal protocol for high throughput analysis of exosomal miRNAs, we compared three different urinary exosomes isolation methods and six RNA extraction techniques. Exosomal RNA yield, size and quality were assessed respectively by specific staining with fluorescent dye, capillary electrophoresis and analysis of spectrophotometric parameters. MiRNAs detection and abundance was determined by RT-qPCR.

Results: Among the exosomes isolation methods, Ultrafiltration resulted to be the most suited. The highest exosomal RNA yield quantified by RiboGreen® staining was obtained with the combination of TRI Reagent™ with miRNeasy®, followed by TRI Reagent™, SeraMir™, miRCURY™, mirVana™ and miRNeasy®; but after a multivariate analysis, SeraMir™ scored as the method of choice in terms of miRNA yield, purity and RT-qPCR miRNAs quantification accuracy. Storage conditions were also analyzed, showing that the relative abundance of urinary exosomal miRNAs is not influenced by urine freezing.

Conclusions: The selection of appropriate urinary exosomal miRNA isolation method was dependent on various validation results. Ultrafiltration in combination with SeraMir™ exoRNA columns represents the optimal procedure for a rapid, cost-effective and efficient purification of miRNAs from urinary exosomes, perfectly suited for further applicative research in the field of miRNAs in kidney physiology and pathology.


Corresponding author: Prof. Oliviero Olivieri, MD, Department of Medicine, Unit of Internal Medicine, University of Verona, Policlinico G.B. Rossi, Piazzale L.A. Scuro 10, 37134 Verona, Italy, Phone: +39 0458124401, Fax: +39 0458027473, E-mail:

This study was supported by research grants of the Ministero dell’Istruzione dell’Università e della Ricerca (PRIN projects 200999KRFW_004), the University of Verona (Joint Project_2010 grant), Fondazione Cariverona (“Verona nano-medicine initiative” project).

Conflict of interest statement

Authors’ conflict of interest disclosure: The authors stated that there are no conflicts of interest regarding the publication of this article. Research funding played no role in the study design, in the collection, analysis, and interpretation of data, in the writing of the report or in the decision to submit the report for publication.

Research funding: None declared.

Employment or leadership: None declared.

Honorarium: None declared.

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Received: 2013-07-18
Accepted: 2013-08-27
Published Online: 2013-10-05
Published in Print: 2014-03-01

©2014 by Walter de Gruyter Berlin Boston

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