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Exogenous loading of miRNAs into small extracellular vesicles
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. He...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8329988/ https://www.ncbi.nlm.nih.gov/pubmed/34377372 http://dx.doi.org/10.1002/jev2.12111 |
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author | de Abreu, Ricardo C. Ramos, Cristiana V. Becher, Clarissa Lino, Miguel Jesus, Carlos da Costa Martins, Paula A. Martins, Patrícia A. T. Moreno, Maria João Fernandes, Hugo Ferreira, Lino |
author_facet | de Abreu, Ricardo C. Ramos, Cristiana V. Becher, Clarissa Lino, Miguel Jesus, Carlos da Costa Martins, Paula A. Martins, Patrícia A. T. Moreno, Maria João Fernandes, Hugo Ferreira, Lino |
author_sort | de Abreu, Ricardo C. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-8329988 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-83299882021-08-09 Exogenous loading of miRNAs into small extracellular vesicles de Abreu, Ricardo C. Ramos, Cristiana V. Becher, Clarissa Lino, Miguel Jesus, Carlos da Costa Martins, Paula A. Martins, Patrícia A. T. Moreno, Maria João Fernandes, Hugo Ferreira, Lino J Extracell Vesicles Short Communication 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. John Wiley and Sons Inc. 2021-08-02 2021-08 /pmc/articles/PMC8329988/ /pubmed/34377372 http://dx.doi.org/10.1002/jev2.12111 Text en © 2021 The Authors. Journal of Extracellular Vesicles published by Wiley Periodicals, LLC on behalf of the International Society for Extracellular Vesicles https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Communication de Abreu, Ricardo C. Ramos, Cristiana V. Becher, Clarissa Lino, Miguel Jesus, Carlos da Costa Martins, Paula A. Martins, Patrícia A. T. Moreno, Maria João Fernandes, Hugo Ferreira, Lino Exogenous loading of miRNAs into small extracellular vesicles |
title | Exogenous loading of miRNAs into small extracellular vesicles |
title_full | Exogenous loading of miRNAs into small extracellular vesicles |
title_fullStr | Exogenous loading of miRNAs into small extracellular vesicles |
title_full_unstemmed | Exogenous loading of miRNAs into small extracellular vesicles |
title_short | Exogenous loading of miRNAs into small extracellular vesicles |
title_sort | exogenous loading of mirnas into small extracellular vesicles |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8329988/ https://www.ncbi.nlm.nih.gov/pubmed/34377372 http://dx.doi.org/10.1002/jev2.12111 |
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