4.7 Article

Delivery of functional exogenous proteins by plant-derived vesicles to human cells in vitro

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SCIENTIFIC REPORTS
卷 11, 期 1, 页码 -

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NATURE PORTFOLIO
DOI: 10.1038/s41598-021-85833-y

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  1. Resource Center for Probe and Electron Microscopy at the NRC Kurchatov Institute
  2. Russian Science Foundation [19-74-20146]
  3. Russian Foundation for Basic Research [18-29-09101]
  4. Ministry of Science and Higher Education of the Russian Federation [0657-2020-0004]
  5. Russian Science Foundation [19-74-20146] Funding Source: Russian Science Foundation

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Plant-derived extracellular vesicles (EVs) are gaining attention as promising carriers for delivering exogenous bioactive molecules to human cells. In this study, grapefruit EVs were isolated and characterized, showing efficient delivery of proteins to human cells and significant uptake by organs in mice. These findings suggest that native plant EVs could be safe and effective carriers for exogenous proteins.
Plant-derived extracellular vesicles (EVs) gain more and more attention as promising carriers of exogenous bioactive molecules to the human cells. Derived from various edible sources, these EVs are remarkably biocompatible, biodegradable and highly abundant from plants. In this work, EVs from grapefruit juice were isolated by differential centrifugation followed by characterization of their size, quantity and morphology by nanoparticle tracking analysis, dynamic light scattering, atomic force microscopy and cryo-electron microscopy (Cryo-EM). In Cryo-EM experiments, we visualized grapefruit EVs with the average size of 41 +/- 13 nm, confirmed their round-shaped morphology and estimated the thickness of their lipid bilayer as 5.3 +/- 0.8 nm. Further, using cell culture models, we have successfully demonstrated that native grapefruit-derived extracellular vesicles (GF-EVs) are highly efficient carriers for the delivery of the exogenous Alexa Fluor 647 labeled bovine serum albumin (BSA) and heat shock protein 70 (HSP70) into both human peripheral blood mononuclear cells and colon cancer cells. Interestingly, loading to plant EVs significantly ameliorated the uptake of exogenous proteins by human cells compared to the same proteins without EVs. Most importantly, we have confirmed the functional activity of human recombinant HSP70 in the colon cancer cell culture upon delivery by GF-EVs. Analysis of the biodistribution of GF-EVs loaded with I-125-labeled BSA in mice demonstrated a significant uptake of the grapefruit-derived extracellular vesicles by the majority of organs. The results of our study indicate that native plant EVs might be safe and effective carriers of exogenous proteins into human cells.

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