Plant-derived extracellular vesicles: a novel nanomedicine approach with advantages and challenges.


Journal

Cell communication and signaling : CCS
ISSN: 1478-811X
Titre abrégé: Cell Commun Signal
Pays: England
ID NLM: 101170464

Informations de publication

Date de publication:
23 05 2022
Historique:
received: 14 12 2021
accepted: 28 04 2022
entrez: 23 5 2022
pubmed: 24 5 2022
medline: 26 5 2022
Statut: epublish

Résumé

Many eukaryote cells produce membrane-enclosed extracellular vesicles (EVs) to establish cell-to-cell communication. Plant-derived EVs (P-EVs) contain proteins, RNAs, lipids, and other metabolites that can be isolated from the juice, the flesh, and roots of many species. In the present review study, we studied numerous articles over the past two decades published on the role of P-EVs in plant physiology as well as on the application of these vesicles in different diseases. Different types of EVs have been identified in plants that have multiple functions including reorganization of cell structure, development, facilitating crosstalk between plants and fungi, plant immunity, defense against pathogens. Purified from several edible species, these EVs are more biocompatible, biodegradable, and extremely available from many plants, making them useful for cell-free therapy. Emerging evidence of clinical and preclinical studies suggest that P-EVs have numerous benefits over conventional synthetic carriers, opening novel frontiers for the novel drug-delivery system. Exciting new opportunities, including designing drug-loaded P-EVs to improve the drug-delivery systems, are already being examined, however clinical translation of P-EVs-based therapies faces challenges. P-EVs hold great promise for clinical application in the treatment of different diseases. In addition, despite enthusiastic results, further scrutiny should focus on unravelling the detailed mechanism behind P-EVs biogenesis and trafficking as well as their therapeutic applications. Video Abstract.

Sections du résumé

BACKGROUND
Many eukaryote cells produce membrane-enclosed extracellular vesicles (EVs) to establish cell-to-cell communication. Plant-derived EVs (P-EVs) contain proteins, RNAs, lipids, and other metabolites that can be isolated from the juice, the flesh, and roots of many species.
METHODS
In the present review study, we studied numerous articles over the past two decades published on the role of P-EVs in plant physiology as well as on the application of these vesicles in different diseases.
RESULTS
Different types of EVs have been identified in plants that have multiple functions including reorganization of cell structure, development, facilitating crosstalk between plants and fungi, plant immunity, defense against pathogens. Purified from several edible species, these EVs are more biocompatible, biodegradable, and extremely available from many plants, making them useful for cell-free therapy. Emerging evidence of clinical and preclinical studies suggest that P-EVs have numerous benefits over conventional synthetic carriers, opening novel frontiers for the novel drug-delivery system. Exciting new opportunities, including designing drug-loaded P-EVs to improve the drug-delivery systems, are already being examined, however clinical translation of P-EVs-based therapies faces challenges.
CONCLUSION
P-EVs hold great promise for clinical application in the treatment of different diseases. In addition, despite enthusiastic results, further scrutiny should focus on unravelling the detailed mechanism behind P-EVs biogenesis and trafficking as well as their therapeutic applications. Video Abstract.

Identifiants

pubmed: 35606749
doi: 10.1186/s12964-022-00889-1
pii: 10.1186/s12964-022-00889-1
pmc: PMC9128143
doi:

Types de publication

Journal Article Review Video-Audio Media

Langues

eng

Sous-ensembles de citation

IM

Pagination

69

Informations de copyright

© 2022. The Author(s).

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Auteurs

Mohadeseh Nemati (M)

Department of Biochemistry, School of Medicine, Urmia University of Medical Sciences, Urmia, Iran.

Bipin Singh (B)

Department of Biotechnology, School of Engineering and Applied Sciences, Bennett University, Greater Noida, Uttar Pradesh, 201310, India.

Rakeeb Ahmad Mir (RA)

Department of Biotechnology, School of Bio-Sciences and Biotechnology Baba Ghulam, Shah Badshah University, Rajouri, Jammu & Kashmir, 185234, India.

Mahdieh Nemati (M)

Department of Medical Nanotechnology, Faculty of Advanced Medical Science, Tabriz University of Medical Sciences, Tabriz, Iran.

Azadeh Babaei (A)

Department of Anatomical Sciences, Faculty of Medical Science, Tarbiat Modares University, Tehran, Iran.

Mahdi Ahmadi (M)

Drug Applied Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.

Yousef Rasmi (Y)

Department of Biochemistry, School of Medicine, Urmia University of Medical Sciences, Urmia, Iran. rasmiy@umsu.ac.ir.
Cellular and Molecular Research Center, Urmia University of Medical Sciences, Urmia, Iran. rasmiy@umsu.ac.ir.

Afsaneh Gholinejad Golezani (AG)

Solid Tumor Research Center, Cellular and Molecular Medicine Institute, Urmia University of Medical Sciences, Shafa St, Ershad Blvd., P.O. Box: 1138, Urmia, 57147, Iran.

Jafar Rezaie (J)

Solid Tumor Research Center, Cellular and Molecular Medicine Institute, Urmia University of Medical Sciences, Shafa St, Ershad Blvd., P.O. Box: 1138, Urmia, 57147, Iran. J.rezaie88@gmail.com.

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