Department of Neurosurgery, University of Kentucky College of Medicine, Lexington, KY; University of Kentucky Nanobiotechnology Center, Lexington, KY.
Department of Neurosurgery, University of Kentucky College of Medicine, Lexington, KY.
Nanomedicine. 2017 Oct;13(7):2209-2217. doi: 10.1016/j.nano.2017.06.010. Epub 2017 Jun 27.
This study reports proof of concept for administering compacted DNA nanoparticles (DNPs) intracerebrally as a means to protect against neurotoxin-induced neurodegeneration of dopamine (DA) neurons. In this study we used DNPs that encoded for human glial cell line-derived neurotrophic factor (hGDNF); GDNF is a potent neurotrophic factor for DA neurons. Intracerebral injections of DNPs into the striatum and/or substantia nigra were performed 1 week before treatment with a neurotoxin. We observed that the number of surviving DA cells, the density of DA fiber terminals and recovery of motor function were greater in animals injected with GDNF-encoding DNPs than in control animals receiving DNPs encoding for an inert reporter gene. The results of these studies are one of the first to demonstrate that a non-viral, synthetic nanoparticle can be used to deliver therapeutic genes to cells in the brain as a means to protect cells against neurotoxin-induced neurodegeneration.
本研究报告了一个概念验证,即将压缩的 DNA 纳米颗粒(DNPs)脑内给药作为一种防止神经毒素诱导多巴胺(DA)神经元变性的方法。在这项研究中,我们使用了编码人胶质细胞系源性神经营养因子(hGDNF)的 DNPs;GDNF 是一种有效的 DA 神经元神经营养因子。在使用神经毒素治疗前一周,通过脑内注射将 DNPs 注入纹状体和/或黑质。我们观察到,与接受编码惰性报告基因的 DNPs 的对照动物相比,注射编码 GDNF 的 DNPs 的动物中存活的 DA 细胞数量、DA 纤维末梢密度和运动功能恢复更大。这些研究的结果是首次证明非病毒、合成纳米颗粒可用于将治疗基因递送到大脑中的细胞,作为防止细胞免受神经毒素诱导的神经变性的一种手段。