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Long-term inducible expression in striatal neurons from helper virus-free HSV-1 vectors that contain the tetracycline-inducible promoter system

机译:含有四环素诱导型启动子系统的无辅助病毒HSV-1载体在纹状体神经元中的长期诱导表达

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摘要

Direct gene transfer into neurons in the brain via a virus vector system has potential for both examining neuronal physiology and for developing gene therapy treatments for neurological diseases. Many of these applications require precise control of the levels of recombinant gene expression. The preferred method for controlling the levels of expression is by use of an inducible promoter system, and the tetracycline (tet)-inducible promoter system is the preferred system. Helper virus-free Herpes Simplex Virus (HSV-1) vectors have a number of the advantages, including their large size and efficient gene transfer. Also, we have reported long-term (14 months) expression from HSV-1 vectors that contain a modified neurofilament heavy gene promoter. A number of studies have reported short-term, inducible expression from helper virus-containing HSV-1 vector systems. However, long-term, inducible expression has not been reported using HSV-1 vectors. The goal of this study was to obtain long-term, inducible expression from helper virus-free HSV-1 vectors. We examined two different vector designs for adapting the tet promoter system to HSV-1 vectors. One design was an autoregulatory design; one transcription unit used a tet-regulated promoter to express the tet-regulated transcription factor tet-off, and another transcription unit used a tet-regulated promoter to express the Lac Z gene. In the other vector design, one transcription unit used the modified neurofilament heavy gene promoter to express tet-off, and another transcription unit used a tet-regulated promoter to express the Lac Z gene. The results showed that both vector designs supported inducible expression in cultured fibroblast or neuronal cell lines and for a short time (4 days) in the rat striatum. Of note, only the vector design that used the modified neurofilament promoter to express tet-off supported long-term (2 months) inducible expression in striatal neurons.
机译:通过病毒载体系统将基因直接转移到大脑中的神经元中,既有可能检查神经元生理学,又有可能开发针对神经疾病的基因疗法。这些应用中的许多都需要精确控制重组基因表达的水平。控制表达水平的优选方法是使用诱导型启动子系统,而四环素(tet)诱导型启动子系统是优选的系统。无辅助病毒的单纯疱疹病毒(HSV-1)载体具有许多优点,包括它们的大尺寸和有效的基因转移。另外,我们已经报道了含有修饰的神经丝重基因启动子的HSV-1载体的长期表达(14个月)。许多研究报告了含有辅助病毒的HSV-1载体系统的短期诱导表达。然而,尚未报道使用HSV-1载体的长期诱导型表达。这项研究的目的是从无辅助病毒的HSV-1载体中获得长期的诱导型表达。我们检查了两种不同的载体设计,以使tet启动子系统适应HSV-1载体。一种设计是自动调节设计。一个转录单位使用tet调控的启动子来表达tet调控的转录因子tet-off,另一个转录单位使用tet调控的启动子来表达Lac Z基因。在另一种载体设计中,一个转录单位使用修饰的神经丝重基因启动子表达tet-off,另一个转录单位使用tet调节的启动子表达Lac Z基因。结果表明,两种载体设计均支持在培养的成纤维细胞或神经元细胞系中以及大鼠纹状体中短时间(4天)的诱导表达。值得注意的是,只有使用修饰的神经丝启动子表达tet-off的载体设计支持纹状体神经元中的长期(2个月)诱导型表达。

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