Torashima Takashi, Yamada Nobuaki, Itoh Masae, Yamamoto Akitsugu, Hirai Hirokazu
Innovative Brain Science Project, Advanced Science Research Center, Kanazawa University, Kanazawa 920-8640, Japan.
Eur J Neurosci. 2006 Jul;24(2):371-80. doi: 10.1111/j.1460-9568.2006.04927.x. Epub 2006 Jul 12.
Cerebellar Purkinje cells play an important role in cerebellar function; lesions of Purkinje cells result in the disruption of motor coordination and motor learning. Although selective gene delivery to Purkinje cells would be a powerful technique for the study of pathophysiology in the cerebellum, a method for such a delivery has not yet been established. Here we employed human immunodeficiency virus-derived lentiviral vectors pseudotyped with vesicular stomatitis virus glycoprotein to transduce Purkinje cells and examined factors that critically affect the viral tropism for Purkinje cells. Viral vectors encoding GFP were generated using different protocols, and were then injected into the mouse cerebellum. At 7 days and 2 months post-transduction, the relative proportions of transduced Purkinje cells were determined. Lentiviral vectors harvested from a medium of pH 7.2 preferentially transduced Purkinje cells (about half of the transduced cells). In contrast, when the viral vector was harvested from medium of <or= pH 7.0, only 12-26% of transduced cells were identified as Purkinje cells and 68-77% as Bergmann glia. A similar decrease in the efficiency of transduction for Purkinje cells, depending on the pH of the medium at the viral harvest, was observed in dissociated cell cultures. These results indicate that lentivector tropism for Purkinje cells is extremely sensitive to pH: a subtle decrease in the pH of the medium at the harvest shifts viral tropism strikingly towards Bergmann glia.
小脑浦肯野细胞在小脑功能中发挥着重要作用;浦肯野细胞损伤会导致运动协调和运动学习的破坏。尽管向浦肯野细胞进行选择性基因传递将是研究小脑病理生理学的一项强大技术,但尚未建立这样一种传递方法。在这里,我们使用水疱性口炎病毒糖蛋白假型化的人免疫缺陷病毒衍生慢病毒载体转导浦肯野细胞,并研究了严重影响病毒对浦肯野细胞嗜性的因素。使用不同方案生成编码绿色荧光蛋白(GFP)的病毒载体,然后将其注射到小鼠小脑中。在转导后7天和2个月,确定转导的浦肯野细胞的相对比例。从pH 7.2的培养基中收获的慢病毒载体优先转导浦肯野细胞(约一半的转导细胞)。相比之下,当从pH≤7.0的培养基中收获病毒载体时,只有12 - 26%的转导细胞被鉴定为浦肯野细胞,68 - 77%为伯格曼胶质细胞。在解离细胞培养物中也观察到,根据收获时培养基的pH值,浦肯野细胞的转导效率有类似的降低。这些结果表明,慢病毒载体对浦肯野细胞的嗜性对pH极其敏感:收获时培养基pH值的细微降低会使病毒嗜性显著转向伯格曼胶质细胞。