Glud Andreas Nørgaard, Hedegaard Claus, Nielsen Mette Slot, Søorensen Jens Christian, Bendixen Christian, Jensen Poul Henning, Mogensen Poul Henning, Larsen Knud, Bjarkam Carsten Reidies
Institute of Biomedicine, Faculty of Health Sciences, University of Aarhus, Aarhus, Denmark.
Acta Neurobiol Exp (Wars). 2011;71(4):508-18. doi: 10.55782/ane-2011-1867.
The aim was to establish a non-primate large animal PD model by lentiviral vector mediated mutant alpha-synuclein overexpression in the substantia nigra. Lentivirus encoding A53T alpha-synuclein (6 x 2.5 μl) was stereotaxically injected into the substantia nigra of six adult female Göttingen minipigs. Contralateral control injections encoding enhanced green fluorescent protein (EGFP) were performed. Gait-analysis was performed pre- and postoperatively. PCR of the transgenes and immunohistochemical staining against alpha-synuclein, EGFP, GFAP and TH was performed after 20 weeks. Gait analysis revealed a significant increase in step length and height, and a decrease in the double stand phase. PCR verified the mesencephalic presence of transgenes. IHC analysis showed alpha-synuclein expression in nigral neurons, around the injection tract and in related nigrostriatal projections. The alpha-synuclein positive neurons appeared swollen and vacuolated, in contrast to the EGFP-injected control side. To transduct all nigrostriatal cells with few microinjections, wider dissemination of the transgene must be achieved.
目的是通过慢病毒载体介导突变型α-突触核蛋白在黑质中过表达来建立一种非灵长类大型动物帕金森病(PD)模型。将编码A53Tα-突触核蛋白的慢病毒(6×2.5微升)立体定向注射到6只成年雌性哥廷根小型猪的黑质中。对侧进行编码增强型绿色荧光蛋白(EGFP)的对照注射。在术前和术后进行步态分析。20周后进行转基因的PCR以及针对α-突触核蛋白、EGFP、胶质纤维酸性蛋白(GFAP)和酪氨酸羟化酶(TH)的免疫组织化学染色。步态分析显示步长和步高显著增加,双支撑期减少。PCR证实转基因存在于中脑。免疫组织化学分析显示α-突触核蛋白在黑质神经元、注射部位周围以及相关黑质纹状体投射中表达。与注射EGFP的对照侧相比,α-突触核蛋白阳性神经元出现肿胀和空泡化。为了通过少量微注射转导所有黑质纹状体细胞,必须实现转基因更广泛的传播。