Green fluorescent protein as a reporter for retrovirus and helper virus-free HSV-1 amplicon vector-mediated gene transfer into neural cells in culture and in vivo

被引:33
作者
AboodyGuterman, KS
Pechan, PA
Rainov, NG
SenaEsteves, M
Jacobs, A
Snyder, EY
Wild, P
Schraner, E
Tobler, K
Breakefield, XO
Fraefel, C
机构
[1] HARVARD UNIV,SCH MED,CHILDRENS HOSP,DEPT NEUROL,BOSTON,MA
[2] MASSACHUSETTS GEN HOSP,NEUROL SERV,MOL NEUROGENET UNIT,BOSTON,MA 02114
[3] MASSACHUSETTS GEN HOSP,PROGRAM NEUROSCI,BOSTON,MA 02114
[4] HARVARD UNIV,SCH MED,CHILDRENS HOSP,DEPT PEDIAT,BOSTON,MA
[5] UNIV ZURICH,INST ANAT,ZURICH,SWITZERLAND
[6] UNIV ZURICH,INST VIROL,ZURICH,SWITZERLAND
[7] UNIV HALLE WITTENBERG,DEPT NEUROSURG,D-06097 HALLE,GERMANY
[8] NORTHWESTERN UNIV,BMBCB,EVANSTON,IL 60208
关键词
CNS; gene transfer; green fluorescent protein; gliomas; helper virus free HSV-1 amplicon vector; neural progenitor cells; retrovirus vector;
D O I
10.1097/00001756-199712010-00029
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
GREEN fluorescent protein (GFP) is an effective marker for retrovirus and herpes virus vector-mediated gene transfer into various central nervous system-derived cells, both proliferative and non-proliferative, in culture and in vivo. Retrovirus vectors were used to stably transduce several rat and human glioma lines, and a multipotent mouse neural progenitor line in culture. Implantation of selected pools of transduced glioma cells into rodent brain allowed clear visualization of the tumor and the invading tumor edge. Helper virus-free HSV-1 amplicon vectors successfully transferred gfp into non-dividing primary neural cells in culture and in the rat brain. This study describes the versatility of GFP for: (i) labelling of glioma cells in experimental brain tumor models and neural progenitor cells by retrovirus vectors, and (ii) efficient, non-toxic delivery of genes to Post mitotic cells of the nervous system using helper-virus free HSV-1 amplicon vectors.
引用
收藏
页码:3801 / 3808
页数:8
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