4.7 Article

Exogenous loading of miRNAs into small extracellular vesicles

Journal

JOURNAL OF EXTRACELLULAR VESICLES
Volume 10, Issue 10, Pages -

Publisher

WILEY
DOI: 10.1002/jev2.12111

Keywords

extracellular vesicles; microRNA; modulation; post-isolation

Categories

Funding

  1. Portuguese 'Fundacao para a Ciencia e a Tecnologia' (FCT) [007630 UID/QUI/00313/2019, PT2020_PTDC_DTP-FTO_2784_2014, POCI-01-0145-FEDER-029919]
  2. COMPETE2020-UE
  3. 'Programa Operacional Regional do Centro' CENTRO2020 [CENTRO-01-0145-FEDER-000014]
  4. European Union [952266]
  5. FCT [SFRH/BD/129317/2017]
  6. [EAPA_791/2018]
  7. Fundação para a Ciência e a Tecnologia [SFRH/BD/129317/2017] Funding Source: FCT

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The study demonstrates that Exo-Fect is the most efficient method for modulating sEVs, leading to over 1000-fold upregulation of the miRNA of interest and successful delivery of miR-155-5p into target cells, demonstrating its functionality. Furthermore, the membrane alterations in Exo-Fect-loaded sEVs enhance internalization within target cells and decrease interaction with lysosomes.
Small extracellular vesicles (sEVs), through their natural ability to interact with biological membranes and exploit endogenous processing pathways to convey biological information, are quintessential for the delivery of therapeutically relevant compounds, such as microRNAs (miRNAs) and proteins. Here, we used a fluorescently-labelled miRNA to quantify the efficiency of different methods to modulate the cargo of sEVs. Our results showed that, compared with electroporation, heat shock, permeation by a detergent-based compound (saponin) or cholesterol-modification of the miRNA, Exo-Fect was the most efficient method with > 50% transfection efficiency. Furthermore, qRT-PCR data showed that, compared with native sEVs, Exo-Fect modulation led to a > 1000-fold upregulation of the miRNA of interest. Importantly, this upregulation was observed for sEVs isolated from multiple sources. The modulated sEVs were able to delivery miR-155-5p into a reporter cell line, confirming the successful delivery of the miRNA to the target cell and, more importantly, its functionality. Finally, we showed that the membrane of Exo-Fect-loaded sEVs was altered compared with native sEVs and that enhanced the internalization of Exo-Fect-loaded sEVs within the target cells and decreased the interaction of those modulated sEVs with lysosomes.

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