Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2020 Oct 14:8:584391.
doi: 10.3389/fbioe.2020.584391. eCollection 2020.

Plant-Derived Nanovesicles: A Novel Form of Nanomedicine

Affiliations
Review

Plant-Derived Nanovesicles: A Novel Form of Nanomedicine

Lanlan Yu et al. Front Bioeng Biotechnol. .

Abstract

The nanovesicles extracted from the plant and herbal decoctions are identified as a new class of nanomedicine. They are involved in interspecies chemical communication across the plant and animal kingdoms and display a therapeutic potential against a variety of diseases. Herein, we review the recent progress made in the medical applications of plant-derived nanovesicles in the aspects of anti-inflammation, anti-cancer, tissue regeneration, and modulating commensal microbiota. We further summarize the cellular and molecular mechanisms underlying the physiological functions of plant-derived nanovesicles. Overall, plant-derived nanovesicles provide an alternative to conventional synthetic drugs and present exciting opportunities for future research on disease therapy.

Keywords: bioeffects of nanomaterials; cross-kingdom gene regulation; nanomedicine; plant-derived nanovesicles; small RNAs.

PubMed Disclaimer

Figures

FIGURE 1
FIGURE 1
Schematic representations of medical applications of plant-derived nanovesicles (A) in inflammation regulation, (B) in anticancer, (C) in tissue renewal and remodeling, (D) in modulating commensal microbiota.

Similar articles

Cited by

References

    1. AbdElgawad H., Peshev D., Zinta G., Van den Ende W., Janssens I. A., Asard H. (2014). Climate extreme effects on the chemical composition of temperate grassland species under ambient and elevated CO2: a comparison of fructan and non-fructan accumulators. PLoS One 9:e92044. 10.1371/journal.pone.0092044 - DOI - PMC - PubMed
    1. Biswas S. K., Mantovani A. (2010). Macrophage plasticity and interaction with lymphocyte subsets: cancer as a paradigm. Nat. Immunol. 11 889–896. 10.1038/ni.1937 - DOI - PubMed
    1. Broz P., Dixit V. M. (2016). Inflammasomes: mechanism of assembly, regulation and signalling. Nat. Rev. Immunol. 16 407–420. 10.1038/nri.2016.58 - DOI - PubMed
    1. Cao M., Yan H., Han X., Weng L., Wei Q., Sun X., et al. (2019). Ginseng-derived nanoparticles alter macrophage polarization to inhibit melanoma growth. J. ImmunoTher. Cancer 7:326. 10.1186/s40425-019-0817-4 - DOI - PMC - PubMed
    1. Chen F., Wen Q., Jiang J., Li H. L., Tan Y. F., Li Y. H., et al. (2016). Could the gut microbiota reconcile the oral bioavailability conundrum of traditional herbs? J. Ethnopharmacol. 179 253–264. 10.1016/j.jep.2015.12.031 - DOI - PubMed

LinkOut - more resources