Watsuji T, Okamoto Y, Emi N, Katsuoka Y, Hagiwara M
Department of Endocrinology, Medical Research Institute, Tokyo Medical and Dental University, Bunkyo-ku, Japan.
Biochem Biophys Res Commun. 1997 May 29;234(3):769-73. doi: 10.1006/bbrc.1997.6705.
A retroviral vector was constructed with an autoregulatory cassette to allow expression of the gene of interest in response to oral administration of doxycycline (Dox) in vivo. The cassette contains all the components of the reverse tetracycline-regulated (rtTA) system, a drug selectable marker with the internal ribosome entry site and the gene of interest (GFP). FACS analyses showed an induction of GFP-fluorescence of two orders of magnitude in retrovirus-infected 208F cells dependent on the amount of Dox in the medium. Furthermore, oral administration of Dox resulted in GFP expression in transplanted 208F cells in the peritoneal cavity of nude mice. Thus this reverse tetracycline-regulated retroviral vector (RTRV) system simplifies the delivery of controllable genes to cultured and implanted cells. It is hoped that this approach may pave the way to controlled gene expression during a particular window of time in gene therapy applications.
构建了一种逆转录病毒载体,其带有一个自动调节盒,以便在体内口服强力霉素(Dox)后能够表达目的基因。该调节盒包含反向四环素调节(rtTA)系统的所有组件、一个带有内部核糖体进入位点的药物选择标记以及目的基因(绿色荧光蛋白,GFP)。荧光激活细胞分选(FACS)分析表明,在逆转录病毒感染的208F细胞中,GFP荧光的诱导程度取决于培养基中Dox的量,可达两个数量级。此外,口服Dox导致裸鼠腹腔内移植的208F细胞中GFP表达。因此,这种反向四环素调节的逆转录病毒载体(RTRV)系统简化了将可控基因递送至培养细胞和植入细胞的过程。希望这种方法能够为基因治疗应用中特定时间段内的可控基因表达铺平道路。