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      Extracellular microRNAs exhibit sequence-dependent stability and cellular release kinetics

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          ABSTRACT

          Multiple studies have described extracellular microRNAs (ex-miRNAs) as being remarkably stable despite the hostile extracellular environment, when stored at 4ºC or lower. Here we show that many ex-miRNAs are rapidly degraded when incubated at 37ºC in the presence of serum (thereby simulating physiologically relevant conditions). Stability varied widely between miRNAs, with half-lives ranging from ~1.5 hours to more than 13 hours. Notably, ex-miRNA half-lives calculated in two different biofluids (murine serum and C2C12 mouse myotube conditioned medium) were highly similar, suggesting that intrinsic sequence properties are a determining factor in miRNA stability. By contrast, ex-miRNAs associated with extracellular vesicles (isolated by size exclusion chromatography) were highly stable. The release of ex-miRNAs from C2C12 myotubes was measured over time, and mathematical modelling revealed miRNA-specific release kinetics. While some ex-miRNAs reached the steady state in cell culture medium within 24 hours, the extracellular level of miR-16 did not reach equilibrium, even after 3 days in culture. These findings are indicative of miRNA-specific release and degradation kinetics with implications for the utility of ex-miRNAs as biomarkers, and for the potential of ex-miRNAs to transfer gene regulatory information between cells.

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          Most cited references27

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          Muscle-specific microRNA miR-206 promotes muscle differentiation

          Three muscle-specific microRNAs, miR-206, -1, and -133, are induced during differentiation of C2C12 myoblasts in vitro. Transfection of miR-206 promotes differentiation despite the presence of serum, whereas inhibition of the microRNA by antisense oligonucleotide inhibits cell cycle withdrawal and differentiation, which are normally induced by serum deprivation. Among the many mRNAs that are down-regulated by miR-206, the p180 subunit of DNA polymerase α and three other genes are shown to be direct targets. Down-regulation of the polymerase inhibits DNA synthesis, an important component of the differentiation program. The direct targets are decreased by mRNA cleavage that is dependent on predicted microRNA target sites. Unlike small interfering RNA–directed cleavage, however, the 5′ ends of the cleavage fragments are distributed and not confined to the target sites, suggesting involvement of exonucleases in the degradation process. In addition, inhibitors of myogenic transcription factors, Id1-3 and MyoR, are decreased upon miR-206 introduction, suggesting the presence of additional mechanisms by which microRNAs enforce the differentiation program.
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            Ultrafiltration with size-exclusion liquid chromatography for high yield isolation of extracellular vesicles preserving intact biophysical and functional properties.

            Extracellular vesicles (EVs) are natural nanoparticles that mediate intercellular transfer of RNA and proteins and are of great medical interest; serving as novel biomarkers and potential therapeutic agents. However, there is little consensus on the most appropriate method to isolate high-yield and high-purity EVs from various biological fluids. Here, we describe a systematic comparison between two protocols for EV purification: ultrafiltration with subsequent liquid chromatography (UF-LC) and differential ultracentrifugation (UC). A significantly higher EV yield resulted from UF-LC as compared to UC, without affecting vesicle protein composition. Importantly, we provide novel evidence that, in contrast to UC-purified EVs, the biophysical properties of UF-LC-purified EVs are preserved, leading to a different in vivo biodistribution, with less accumulation in lungs. Finally, we show that UF-LC is scalable and adaptable for EV isolation from complex media types such as stem cell media, which is of huge significance for future clinical applications involving EVs.
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              Extracellular miRNAs: the mystery of their origin and function.

              Mature miRNAs are 19-24 nucleotide noncoding RNAs that post-transcriptionally regulate gene expression in living cells by mediating targeted hydrolysis and translation inhibition of mRNAs. In recent years, miRNAs have been detected in a variety of biological fluids as extracellular nuclease-resistant entities. Importantly, extracellular circulating miRNAs are aberrantly expressed in blood plasma or serum during the course of many diseases, including cancer, and are promising noninvasive biomarkers. However, the biological function of extracellular miRNAs remains questionable. In this article, we summarise the current theories regarding extracellular miRNA origin and function, and suggest that these miRNAs are mostly byproducts of cellular activity. Nevertheless, some extracellular miRNA species might also carry cell-cell signaling function. Copyright © 2012 Elsevier Ltd. All rights reserved.
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                Author and article information

                Journal
                RNA Biol
                RNA Biol
                KRNB
                krnb20
                RNA Biology
                Taylor & Francis
                1547-6286
                1555-8584
                May 2019
                5 March 2019
                5 March 2019
                : 16
                : 5
                : 696-706
                Affiliations
                [a ]Department of Physiology, Anatomy and Genetics, University of Oxford , Oxford, UK
                [b ]VIB-UGent Center for Inflammation Research, Department of Biomedical Molecular Biology, Ghent University , Ghent, Belgium
                [c ]Department of Biomedical Molecular Biology, Ghent University , Ghent, Belgium
                [d ]Department of Paediatrics, University of Oxford , Oxford, UK
                [e ]Institute of Technology, University of Tartu , Tartu, Estonia
                [f ]Sanford Burnham Prebys Medical Discovery Institute, Development, Aging and Regeneration Program , La Jolla, CA, USA
                Author notes
                CONTACT Thomas C. Roberts thomas.roberts@ 123456paediatrics.ox.ac.uk Department of Paediatrics, University of Oxford , South Parks Road, Oxford, OX1 3QX, UK
                [*]

                Present address: Bioscience, Oncology, IMED Biotech Unit, AstraZeneca, Cambridge, UK

                Article
                1582956
                10.1080/15476286.2019.1582956
                6546368
                30836828
                5e229d84-c3ed-4c2f-9406-b18e5c73ddde
                © 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 21 January 2019
                : 1 February 2019
                : 11 February 2019
                Page count
                Figures: 4, References: 66, Pages: 11
                Funding
                Funded by: John Fell Fund, University of Oxford 10.13039/501100004789
                Award ID: AVD00160
                Funded by: Medical Research Council 10.13039/501100000265
                Award ID: 1371292
                This work was supported by the John Fell Fund, University of Oxford [AVD00160];Medical Research Council [1371292];
                Categories
                Research Paper

                Molecular biology
                extracellular microrna,ex-mirna,kinetics,serum,half-life,microrna,mirna
                Molecular biology
                extracellular microrna, ex-mirna, kinetics, serum, half-life, microrna, mirna

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