Yurek David M, Fletcher Anita M, Smith George M, Seroogy Kim B, Ziady Assem G, Molter Joseph, Kowalczyk Tomasz H, Padegimas Linas, Cooper Mark J
Department of Neurosurgery, University of Kentucky College of Medicine, Lexington, Kentucky 40536-0305, USA.
Mol Ther. 2009 Apr;17(4):641-50. doi: 10.1038/mt.2009.2. Epub 2009 Feb 17.
This study demonstrates proof of concept for delivery and expression of compacted plasmid DNA in the central nervous system. Plasmid DNA was compacted with polyethylene glycol substituted lysine 30-mer peptides, forming rod-like nanoparticles with diameters between 8 and 11 nm. Here we show that an intracerebral injection of compacted DNA can transfect both neurons and glia, and can produce transgene expression in the striatum for up to 8 weeks, which was at least 100-fold greater than intracerebral injections of naked DNA plasmids. Bioluminescent imaging (BLI) of injected animals at the 11th postinjection week revealed significantly higher transgene activity in animals receiving compacted DNA plasmids when compared to animals receiving naked DNA. There was minimal evidence of brain inflammation. Intrastriatal injections of a compacted plasmid encoding for glial cell line-derived neurotrophic factor (pGDNF) resulted in a significant overexpression of GDNF protein in the striatum 1-3 weeks after injection.
本研究证明了在中枢神经系统中递送和表达压缩质粒DNA的概念验证。质粒DNA与聚乙二醇取代的赖氨酸30聚体肽压缩,形成直径在8至11纳米之间的棒状纳米颗粒。在此我们表明,脑内注射压缩DNA可转染神经元和神经胶质细胞,并可在纹状体中产生长达8周的转基因表达,这比脑内注射裸DNA质粒至少高100倍。注射后第11周对注射动物进行生物发光成像(BLI)显示,与接受裸DNA的动物相比,接受压缩DNA质粒的动物转基因活性显著更高。几乎没有脑炎症的证据。脑内注射编码胶质细胞源性神经营养因子(pGDNF)的压缩质粒导致注射后1至3周纹状体中GDNF蛋白显著过表达。