转基因
生物
突触蛋白I
胶质纤维酸性蛋白
报告基因
分子生物学
基因表达
转基因小鼠
细胞生物学
遗传增强
病毒载体
转染
神经胶质
基因
中枢神经系统
神经科学
遗传学
免疫学
重组DNA
免疫组织化学
小泡
膜
突触小泡
作者
G. Ralph,Alison Bienemann,Tom Harding,Maggie Hopton,Jeremy M. Henley,James B. Uney
出处
期刊:Neuroreport
[Lippincott Williams & Wilkins]
日期:2000-06-01
卷期号:11 (9): 2051-2055
被引量:49
标识
DOI:10.1097/00001756-200006260-00048
摘要
Targeting regulatable transgene expression specifically to neuronal or glial cell populations would facilitate studies of CNS gene function. We have developed the tetracycline (Tet) regulatable adenoviral system by expressing the Tet-off transactivator (tTA) under the control of the neuronal-specific synapsin I promoter and the well characterized glial-specific glial fibrillary acidic protein (GFAP) promoter. Transfection of primary hippocampal cultures demonstrated that the respective promoters restricted reporter transgene expression exclusively to neuronal or glial populations. Delivery of the vectors into adult rat hippocampus resulted in a similar pattern of cell specific transgene expression. These novel vectors provide a highly effective means of directing regulated, cell-specific, transgene expression and as such are important tools for investigations of neuronal and glial cell function and advancing gene therapy studies.
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