Localised non-viral delivery of nucleic acids for nerve regeneration in injured nervous systems.
Electrospinning
Gene delivery
Gene silencing
Neural tissue engineering
RNA interference
Scaffolds
microRNA
siRNA
Journal
Experimental neurology
ISSN: 1090-2430
Titre abrégé: Exp Neurol
Pays: United States
ID NLM: 0370712
Informations de publication
Date de publication:
09 2019
09 2019
Historique:
received:
01
05
2018
revised:
31
08
2018
accepted:
05
09
2018
pubmed:
10
9
2018
medline:
25
2
2020
entrez:
10
9
2018
Statut:
ppublish
Résumé
Axons damaged by traumatic injuries are often unable to spontaneously regenerate in the adult central nervous system (CNS). Although the peripheral nervous system (PNS) has some regenerative capacity, its ability to regrow remains limited across large lesion gaps due to scar tissue formation. Nucleic acid therapy holds the potential of improving regeneration by enhancing the intrinsic growth ability of neurons and overcoming the inhibitory environment that prevents neurite outgrowth. Nucleic acids modulate gene expression by over-expression of neuronal growth factor or silencing growth-inhibitory molecules. Although in vitro outcomes appear promising, the lack of efficient non-viral nucleic acid delivery methods to the nervous system has limited the application of nucleic acid therapeutics to patients. Here, we review the recent development of efficient non-viral nucleic acid delivery platforms, as applied to the nervous system, including the transfection vectors and carriers used, as well as matrices and scaffolds that are currently used. Additionally, we will discuss possible improvements for localised nucleic acid delivery.
Identifiants
pubmed: 30195695
pii: S0014-4886(18)30435-7
doi: 10.1016/j.expneurol.2018.09.003
pii:
doi:
Substances chimiques
Nucleic Acids
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
112820Informations de copyright
Copyright © 2018 Elsevier Inc. All rights reserved.