Hioki Hiroyuki, Kuramoto Eriko, Konno Michiteru, Kameda Hiroshi, Takahashi Yasuhiro, Nakano Takashi, Nakamura Kouichi C, Kaneko Takeshi
Department of Morphological Brain Science, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Neurosci Res. 2009 Feb;63(2):149-54. doi: 10.1016/j.neures.2008.10.010. Epub 2008 Nov 6.
We developed novel lentiviral vectors by using "Tet-Off system" and succeeded in achieving high-level and neuron-specific gene transduction in vivo. One week after viral injection into the rat neostriatum, the GFP expression was almost completely neuron-specific and about 40 times higher than the expression of a conventional lentiviral vector. High transcriptional activity and neuronal specificity were sustained for up to 8 weeks. Furthermore, neuronal processes of the infected neurons were efficiently visualized by adding a plasma membrane-targeting signal to GFP. These results suggest that the present method is valuable for strong gene transduction and clear visualization of neurons in vivo.
我们利用“Tet-Off系统”开发了新型慢病毒载体,并成功在体内实现了高水平的神经元特异性基因转导。将病毒注射到大鼠新纹状体一周后,绿色荧光蛋白(GFP)的表达几乎完全具有神经元特异性,且比传统慢病毒载体的表达高约40倍。高转录活性和神经元特异性可持续长达8周。此外,通过向GFP添加质膜靶向信号,可有效观察到受感染神经元的神经突。这些结果表明,本方法对于在体内进行强基因转导和清晰观察神经元具有重要价值。