Extracellular microRNAs exhibit sequence-dependent stability and cellular release kinetics

Anna Coenen-Stass(University of Oxford), Marie J. Pauwels(Ghent University), Britt Hanson(University of Oxford), Carla Martín Pérez(University of Oxford), Mariana Conceição(University of Oxford), Matthew J. A. Wood(University of Oxford), Imre Mäger(University of Oxford), Thomas C. Roberts(Sanford Burnham Prebys Medical Discovery Institute)
RNA Biology
March 5, 2019
Cited by 76Open Access
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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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