Direct protein transfer to terminally differentiated muscle cells

被引:26
作者
Derer, W
Easwaran, HP
Knopf, CW
Leonhardt, H
Cardoso, MC
机构
[1] Max Delbruck Ctr Mol Med, Franz Volhard Clin, D-13125 Berlin, Germany
[2] Humboldt Univ, Max Planck Delbruck Ctr Mol Med, Franz Volhard Clin, Berlin, Germany
[3] German Canc Res Ctr, D-6900 Heidelberg, Germany
来源
JOURNAL OF MOLECULAR MEDICINE-JMM | 1999年 / 77卷 / 08期
关键词
GFP; muscle; protein delivery; therapy; VP22;
D O I
10.1007/s001099900036
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Recently, a new approach for direct protein transfer to mammalian cells based on the herpes simplex virus type 1 protein VP22 has been described. This protein has the remarkable property of intercellular trafficking, which is independent of direct cell contacts and is also retained when fused to heterologous proteins. However, the spreading has only been described for proliferating cells and has also been controversially discussed. In this study we describe the generation of a GFP-VP22 fusion protein which is able to spread in COS-7 cells after transient transfection. Moreover, we show in coculture experiments with transfected COS-7 cells and C2C12 myotubes that this fusion protein is also able to spread into terminally differentiated skeletal muscle cells. These results suggest that VP22 might be a novel therapeutic tool for direct protein transfer not only in proliferating but also in terminally differentiated cells.
引用
收藏
页码:609 / 613
页数:5
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