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VP22 enhanced intercellular trafficking of HSV thymidine kinase reduced the level of ganciclovir needed to cause suicide cell death
Author(s) -
Liu ChunSheng,
Kong BaiHua,
HuiQin Xia Helen,
Ellem Kay A. O.,
Wei Ming Q.
Publication year - 2001
Publication title -
the journal of gene medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.689
H-Index - 91
eISSN - 1521-2254
pISSN - 1099-498X
DOI - 10.1002/jgm.164
Subject(s) - suicide gene , thymidine kinase , transfection , ganciclovir , bystander effect , microbiology and biotechnology , biology , cytotoxicity , intracellular , cell culture , fusion gene , western blot , genetic enhancement , virology , herpes simplex virus , gene , in vitro , virus , immunology , human cytomegalovirus , biochemistry , genetics
Background The inefficiency of herpes simplex virus thymidine kinase (TK) gene transfer and toxicity of ganciclovir (GCV) at high concentrations in vivo limits the use of this suicide gene therapy approach for the treatment of cancers in clinical settings. To overcome the problem, we have sought evidence of amplification of cytotoxicity by co‐transfer of the TK gene fused with the gene encoding HSV‐1 structural protein VP22 which has a remarkable ability for intercellular trafficking. Methods The expression of the fusion proteins from the chimeric VP22‐TK or VP22‐EGFP genes was shown by Western blot and VP22 promoted TK or EGFP intercellular trafficking by an indirect immunofluorescent assay. The cytotoxicity was demonstrated by a colorimetric cell proliferation assay followed by an assessment of the bystander effect on admixtures of transfected with non‐transfected naive cells. Results Our results show the expression of the VP22 fusion proteins and their spread to varying numbers of bystander cells (up to 30, observed in viable cells with VP22‐EGFP as well as after methanol fixation), confirming that VP22 assisted intercellular trafficking of the fusion proteins. This VP22 promoted TK spreading resulted in killing by 2.5 µg/ml GCV of virtually all cells in cultures that had been transfected at an efficiency of only 27.5%. In contrast, fewer than 80% of cells were killed when transfected with ‘tk alone’ at the same efficiency. The cell killing effect was exponentially dependent on GCV concentration in cells transfected with ‘tk alone’ at GCV concentrations between 0.25 and 0.5 µg/ml, but not those transfected with VP22‐TK, probably due to the continuously variable, high sensitivity of about 50% of cells. Even at low concentration of GCV (0.2 µg/ml), the enhancement of cell killing by VP22 was four‐fold higher in cells transfected with VP22‐TK than in cells transfected with ‘tk alone’. Conclusions VP22 enhanced intercellular trafficking of TK and amplified the TK/GCV killing effect, especially in the lower range of GCV concentrations. This offers a new strategy to enhance the effectiveness of suicide gene therapy for the treatment of cancers. Copyright © 2001 John Wiley & Sons, Ltd.