scholarly journals 925. Novel Fusion Enzymes of Herpes Simplex Virus Thymidine Kinase Mutants and Guanylate Kinase for Improved Cancer Cell Ablation

2006 ◽  
Vol 13 ◽  
pp. S357
Author(s):  
Andressa Ardiani ◽  
Candice Willmon ◽  
Elizabeth Krabbenhoft ◽  
Margaret E. Black
2021 ◽  
Vol 15 ◽  
Author(s):  
Zijian Lou ◽  
Alexander Post ◽  
Christopher E. Rodgers ◽  
Mahmood Chamankhah ◽  
James Hong ◽  
...  

Neural progenitor cell (NPC) transplants are a promising therapy for treating spinal cord injury (SCI), however, their long-term role after engraftment and the relative contribution to ongoing functional recovery remains a key knowledge gap. Selective human cell ablation techniques, currently being developed to improve the safety of progenitor cell transplant therapies in patients, may also be used as tools to probe the regenerative effects attributable to individual grafted cell populations. The Herpes Simplex Virus Thymidine Kinase (HSV-TK) and ganciclovir (GCV) system has been extensively studied in the context of SCI and broader CNS disease. However, the efficacy of brivudine (BVDU), another HSV-TK prodrug with potentially reduced bystander cytotoxic effects and in vivo toxicity, has yet to be investigated for NPC ablation. In this study, we demonstrate successful generation and in vitro ablation of HSV-TK-expressing human iPSC-derived NPCs with a >80% reduction in survival over controls. We validated an HSV-TK and GCV/BVDU synergistic system with iPSC-NPCs using an efficient gene-transfer method and in vivo ablation in a translationally relevant model of SCI. Our findings demonstrate enhanced ablation efficiency and reduced bystander effects when targeting all rapidly dividing cells with combinatorial GCV and BVDU treatment. However, for use in loss of function studies, BVDU alone is optimal due to reduced nonselective cell ablation.


1996 ◽  
Vol 150 (2) ◽  
pp. 265-273 ◽  
Author(s):  
M Markkula ◽  
K Kananen ◽  
P Klemi ◽  
I Huhtaniemi

Abstract The ovarian expression of the endogenous follicle-stimulating hormone β-subunit (FSHβ) and common α-subunit (Cα) genes, and a herpes simplex virus thymidine kinase (tk) transgene, driven by a 2·3 kb bovine FSHβ promoter, was studied in normal and transgenic (tg) mice. tk functions not only as a neutral reporter that enables the study of the promoter function but also as an exogenously inducible toxigene. Reverse transcriptionPCR followed by Southern blot hybridization with a nested probe was used to show the expression of the gene at the mRNA level. Common α-subunit mRNA was detected in the pituitary gland and ovaries of normal adult mice. We have previously detected endogenous FSHβ and tg tk mRNAs in the mouse pituitary, testis and ovary. In this study, the cellular localization of the corresponding proteins was visualized by immunocytochemistry. In normal mouse ovaries a positive reaction with FSHβ and Cα antisera was seen in some of the corpora lutea and most prominently in the interstitial cells. A positive reaction with the tk antiserum was seen in the same cell types of tg mouse ovaries, but not in those of non-tg mice. Cell-ablation-inducing treatment (gancyclovir, 20 mg/kg per day, for 14 days) of tg female mice reduced pituitary FSH concentrations by 52% (P<0·05) but did not affect pituitary LH or plasma gonadotropins compared with non-tg females treated in the same way. A longer period of cell ablation induction (acyclovir 400 mg/kg per day, for 21 days) reduced not only pituitary but also plasma FSH concentrations (55 and 57% respectively; P<0·05) without affecting LH. This treatment also reduced ovarian weight by 38% (P<0·01). In conclusion, our results show first that the endogenous FSHβ and Cα proteins are produced in the mouse ovary. Hence, endogenously synthesized FSH or its subunits may have a role in the paracrine regulation of ovarian function. Secondly, the FSHβ promoter directs the expression of tg tk in the pituitary gonadotrope cells, as shown by specific but partial ablation of FSH-producing cells after induction by gancyclovir and acyclovir. In the ovary, tk protein was localized to the same compartments as the endogenous gonadotropin subunit proteins. This further confirms our finding of ovarian expression of the FSH subunit genes. Journal of Endocrinology (1996) 150, 265–273


1979 ◽  
Vol 7 (4) ◽  
pp. 859-878 ◽  
Author(s):  
N.M. Wilkie ◽  
J.B. Clements ◽  
W. Boll ◽  
N. Mantei ◽  
D. Lonsdale ◽  
...  

1982 ◽  
Vol 2 (4) ◽  
pp. 426-436 ◽  
Author(s):  
C J Tabin ◽  
J W Hoffmann ◽  
S P Goff ◽  
R A Weinberg

We investigated the feasibility of using retroviruses as vectors for transferring DNA sequences into animal cells. The thymidine kinase (tk) gene of herpes simplex virus was chosen as a convenient model. The internal BamHI fragments of a DNA clone of Moloney leukemia virus (MLV) were replaced with a purified BamHI DNA segment containing the tk gene. Chimeric genomes were created carrying the tk insert in both orientations relative to the MLV sequence. Each was transfected into TK- cells along with MLV helper virus, and TK+ colonies were obtained by selection in the presence of hypoxanthine, aminopterin, and thymidine (HAT). Virus collected from TK+-transformed, MLV producer cells passed the TK+ phenotype to TK- cells. Nonproducer cells were isolated, and TK+ transducing virus was subsequently rescued from them. The chimeric virus showed single-hit kinetics in infections. Virion and cellular RNA and cellular DNA from infected cells were all shown to contain sequences which hybridized to both MLV- and tk-specific probes. The sizes of these sequences were consistent with those predicted for the chimeric virus. In all respects studied, the chimeric MLV-tk virus behaved like known replication-defective retroviruses. These experiments suggest great general applicability of retroviruses as eucaryotic vectors.


Virology ◽  
1997 ◽  
Vol 235 (2) ◽  
pp. 398-405 ◽  
Author(s):  
N. Guettari ◽  
L. Loubière ◽  
E. Brisson ◽  
D. Klatzmann

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