Journal
MOLECULAR PHARMACEUTICS
Volume 15, Issue 5, Pages 2060-2067Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.molpharmaceut.7b01084
Keywords
brain; mRNA delivery; nanoparticles; lipid
Funding
- JSPS KAKENHI [15H01806]
- Asahi Glass Foundation
- JST CREST [JPMJCR17H1]
- Grants-in-Aid for Scientific Research [15H01806] Funding Source: KAKEN
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Gene therapy is a promising strategy for curing certain types of brain diseases. Supplementation of therapeutic proteins such as aromatic amino acid decarboxylase (AADC) or nerve growth factor (NGF) have been reported to be successful examples of such treatments. However, there are safety concerns because these systems are based on virus-based gene vectors. A safe and efficient artificial carrier is thus urgently needed as an alternative. In this study, an mRNA based artificial gene carrier was introduced into the mouse brain via intracerebroventricular administration. As a carrier, a lipid nanoparticle (LNP) composed of environmentally sensitive lipid-like materials called an SS-cleavable proton activated lipid-like material is used. The apolipoprotein E mediated cellular uptake of the lipid nanoparticles is one of the key features for its superior and homogeneous transfection activity compared to commercially available transfection reagents in both in vitro and in vivo situations. Immunostaining of brain specimens suggested that exogenous proteins can be introduced into neuronal cells as well as astrocytes using the mRNA-based gene carrier. This cannot be achieved using DNA-based artificial gene carriers. The findings suggest that a combination of an mRNA and a lipid based delivery system have great promise as a platform for the treatment of brain disorders.
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