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Título

Therapeutic potential of plant-derived extracellular vesicles as nanocarriers for exogenous miRNAs

AutorLópez de las Hazas, María Carmen; Tomé-Carneiro, Joao CSIC ORCID; Del Pozo-Acebo, Lorena; Del Saz, Andrea; Chapado, Luis A.; Balaguer, Livia; Rojo, Enrique; Espín de Gea, Juan Carlos CSIC ORCID ; Crespo, Carmen; Moreno, Diego A. CSIC ORCID; Garcia-Viguera, Cristina ; Ordovás, José M.; Visioli, Francesco; D´Avalos, Alberto
Palabras claveExtracellular vesicles
MiRNAs
Exosomes
Plant-derived
RNA-seq
Drug delivery
Polyphenols
Fecha de publicacióndic-2023
EditorElsevier
CitaciónPharmacological Research 198: 106999 (2023)
ResumenCell-to-cell communication strategies include extracellular vesicles (EVs) in plants and animals. The bioactive molecules in a diet rich in vegetables and fruits are associated with disease-preventive effects. Plant-derived EVs (PDEVs) are biogenetically and morphologically comparable to mammalian EVs and transport bioactive molecules, including miRNAs. However, the biological functions of PDEVs are not fully understood, and standard isolation protocols are lacking. Here, PDEVs were isolated from four foods with a combination of ultracentrifugation and size exclusion chromatography, and evaluated as vehicles for enhanced transport of synthetic miRNAs. In addition, the role of food-derived EVs as carriers of dietary (poly)phenols and other secondary metabolites was investigated. EVs from broccoli, pomegranate, apple, and orange were efficiently isolated and characterized. In all four sources, 4 miRNA families were present in tissues and EVs. miRNAs present in broccoli and fruit-derived EVs showed a reduced RNase degradation and were ferried inside exposed cells. EVs transfected with a combination of ath-miR159a, ath-miR162a-3p, ath-miR166b-3p, and ath-miR396b-5p showed toxic effects on human cells, as did natural broccoli EVs alone. PDEVs transport trace amounts of phytochemicals, including flavonoids, anthocyanidins, phenolic acids, or glucosinolates. Thus, PDEVs can act as nanocarriers for functional miRNAs that could be used in RNA-based therapy
Versión del editorhttps://doi.org/10.1016/j.phrs.2023.106999
URIhttp://hdl.handle.net/10261/357060
DOI10.1016/j.phrs.2023.106999
ISSN1043-6618
E-ISSN1096-1186
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