Exosomes for targeted siRNA delivery across biological barriers
- PMID: 22921840
- DOI: 10.1016/j.addr.2012.08.008
Exosomes for targeted siRNA delivery across biological barriers
Abstract
Using oligonucleotide-based drugs to modulate gene expression has opened a new avenue for drug discovery. In particular small interfering RNAs (siRNAs) are being rapidly recognized as promising therapeutic tools, but their poor bioavailability limits the full realization of their clinical potential. In recent years, cumulating evidence has emerged for the role of membrane vesicles, secreted by most cells and found in all body fluids, as key mediators of information transmission between cells. Importantly, a sub-group of these termed exosomes, have recently been shown to contain various RNA species and to mediate their horizontal transfer to neighbouring- or distant recipient cells. Here, we provide a brief overview on membrane vesicles and their role in exchange of genetic information. We also describe how these natural carriers of genetic material can be harnessed to overcome the obstacle of poor delivery and allow efficient systemic delivery of exogenous siRNA across biological barriers such as the blood-brain barrier.
Copyright © 2012 Elsevier B.V. All rights reserved.
Similar articles
-
Exosomes: Natural Carriers for siRNA Delivery.Curr Pharm Des. 2015;21(31):4556-65. doi: 10.2174/138161282131151013190112. Curr Pharm Des. 2015. PMID: 26486142 Review.
-
Exosome-mediated delivery of siRNA in vitro and in vivo.Nat Protoc. 2012 Dec;7(12):2112-26. doi: 10.1038/nprot.2012.131. Epub 2012 Nov 15. Nat Protoc. 2012. PMID: 23154783
-
Delivery of Small Interfering RNA to Inhibit Vascular Endothelial Growth Factor in Zebrafish Using Natural Brain Endothelia Cell-Secreted Exosome Nanovesicles for the Treatment of Brain Cancer.AAPS J. 2017 Mar;19(2):475-486. doi: 10.1208/s12248-016-0015-y. Epub 2016 Nov 23. AAPS J. 2017. PMID: 27882487
-
Exosomes: Nanoparticulate tools for RNA interference and drug delivery.J Cell Physiol. 2017 Jul;232(7):1660-1668. doi: 10.1002/jcp.25766. Epub 2017 Jan 31. J Cell Physiol. 2017. PMID: 28063231 Free PMC article. Review.
-
Exosomes are natural carriers of exogenous siRNA to human cells in vitro.Cell Commun Signal. 2013 Nov 18;11:88. doi: 10.1186/1478-811X-11-88. Cell Commun Signal. 2013. PMID: 24245560 Free PMC article.
Cited by
-
Role of Envelopment in the HEV Life Cycle.Viruses. 2016 Aug 18;8(8):229. doi: 10.3390/v8080229. Viruses. 2016. PMID: 27548201 Free PMC article. Review.
-
Extracellular Vesicles in Physiology, Pathology, and Therapy of the Immune and Central Nervous System, with Focus on Extracellular Vesicles Derived from Mesenchymal Stem Cells as Therapeutic Tools.Front Cell Neurosci. 2016 May 2;10:109. doi: 10.3389/fncel.2016.00109. eCollection 2016. Front Cell Neurosci. 2016. PMID: 27199663 Free PMC article. Review.
-
[Application of Extracellular Vesicles Derived from Vascular Endothelial/Endothelial Progenitor Cells in Tissue Regeneration and Repair].Sichuan Da Xue Xue Bao Yi Xue Ban. 2022 Mar;53(2):355-360. doi: 10.12182/20220360507. Sichuan Da Xue Xue Bao Yi Xue Ban. 2022. PMID: 35332742 Free PMC article. Review. Chinese.
-
Dendritic Cell Membrane-Derived Nanovesicles for Targeted T Cell Activation.ACS Omega. 2022 Dec 9;7(50):46222-46233. doi: 10.1021/acsomega.2c04420. eCollection 2022 Dec 20. ACS Omega. 2022. PMID: 36570199 Free PMC article.
-
IFNγ-stimulated dendritic cell exosomes as a potential therapeutic for remyelination.J Neuroimmunol. 2014 Jan 15;266(1-2):12-23. doi: 10.1016/j.jneuroim.2013.10.014. Epub 2013 Nov 9. J Neuroimmunol. 2014. PMID: 24275061 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources