Yurek D M, Hasselrot U, Cass W A, Sesenoglu-Laird O, Padegimas L, Cooper M J
Department of Neurosurgery, University of Kentucky College of Medicine, Lexington, KY 40536, United States.
Department of Neurosurgery, University of Kentucky College of Medicine, Lexington, KY 40536, United States.
Neuroscience. 2015 Jan 22;284:500-512. doi: 10.1016/j.neuroscience.2014.10.026. Epub 2014 Oct 22.
In previous studies that used compacted DNA nanoparticles (DNP) to transfect cells in the brain, we observed higher transgene expression in the denervated striatum when compared to transgene expression in the intact striatum. We also observed that long-term transgene expression occurred in astrocytes as well as neurons. Based on these findings, we hypothesized that the higher transgene expression observed in the denervated striatum may be a function of increased gliosis. Several aging studies have also reported an increase of gliosis as a function of normal aging. In this study we used DNPs that encoded for human glial cell line-derived neurotrophic factor (hGDNF) and either a non-specific human polyubiquitin C (UbC) or an astrocyte-specific human glial fibrillary acidic protein (GFAP) promoter. The DNPs were injected intracerebrally into the denervated or intact striatum of young, middle-aged or aged rats, and glial cell line-derived neurotrophic factor (GDNF) transgene expression was subsequently quantified in brain tissue samples. The results of our studies confirmed our earlier finding that transgene expression was higher in the denervated striatum when compared to intact striatum for DNPs incorporating either promoter. In addition, we observed significantly higher transgene expression in the denervated striatum of old rats when compared to young rats following injections of both types of DNPs. Stereological analysis of GFAP+ cells in the striatum confirmed an increase of GFAP+ cells in the denervated striatum when compared to the intact striatum and also an age-related increase; importantly, increases in GFAP+ cells closely matched the increases in GDNF transgene levels. Thus neurodegeneration and aging may lay a foundation that is actually beneficial for this particular type of gene therapy while other gene therapy techniques that target neurons are actually targeting cells that are decreasing as the disease progresses.
在以往使用致密DNA纳米颗粒(DNP)转染脑内细胞的研究中,我们观察到,与完整纹状体中的转基因表达相比,去神经支配的纹状体中的转基因表达更高。我们还观察到,长期转基因表达发生在星形胶质细胞以及神经元中。基于这些发现,我们推测,在去神经支配的纹状体中观察到的较高转基因表达可能是胶质增生增加的一种表现。多项衰老研究也报告称,胶质增生会随着正常衰老而增加。在本研究中,我们使用了编码人胶质细胞系源性神经营养因子(hGDNF)的DNP,并采用了非特异性人多聚泛素C(UbC)或星形胶质细胞特异性人胶质纤维酸性蛋白(GFAP)启动子。将DNP脑内注射到年轻、中年或老年大鼠的去神经支配或完整纹状体中,随后对脑组织样本中的胶质细胞系源性神经营养因子(GDNF)转基因表达进行定量。我们的研究结果证实了我们早期的发现,即对于包含任何一种启动子的DNP,去神经支配的纹状体中的转基因表达均高于完整纹状体。此外,在注射两种类型的DNP后,我们观察到老年大鼠去神经支配的纹状体中的转基因表达明显高于年轻大鼠。对纹状体中GFAP+细胞的体视学分析证实,与完整纹状体相比,去神经支配的纹状体中GFAP+细胞增加,并且存在与年龄相关的增加;重要的是,GFAP+细胞的增加与GDNF转基因水平的增加密切匹配。因此,神经退行性变和衰老可能为这种特定类型的基因治疗奠定了实际上有益的基础,而其他针对神经元的基因治疗技术实际上针对的是随着疾病进展而减少的细胞。