Targeted Elimination of Tumorigenic Human Pluripotent Stem Cells Using Suicide-Inducing Virus-like Particles

被引:16
作者
Rampoldi, Antonio [1 ,2 ]
Crooke, Stephen N. [3 ]
Preininger, Marcela K. [1 ,2 ,4 ,5 ]
Jha, Rajneesh [1 ,2 ]
Maxwell, Joshua [1 ,2 ]
Ding, Lingmei [1 ,2 ]
Spearman, Paul [1 ,2 ]
Finn, M. G. [3 ,6 ]
Xu, Chunhui [1 ,2 ,4 ,5 ]
机构
[1] Emory Univ, Sch Med, Dept Pediat, Atlanta, GA 30322 USA
[2] Childrens Healthcare Atlanta, Atlanta, GA 30322 USA
[3] Georgia Inst Technol, Sch Chem & Biochem, Atlanta, GA 30318 USA
[4] Georgia Inst Technol, Wallace H Coulter Dept Biomed Engn, Atlanta, GA 30332 USA
[5] Emory Univ, Atlanta, GA 30332 USA
[6] Georgia Inst Technol, Sch Biol Sci, Atlanta, GA 30332 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
SELECTIVE ABLATION; BINDING DOMAIN; CARDIOMYOCYTES; DIFFERENTIATION; GROWTH; MOUSE; GENE;
D O I
10.1021/acschembio.8b00490
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Sensitization to prodrugs via transgenic expression of suicide genes is a leading strategy for the selective elimination of potentially tumorigenic human pluripotent stem cells (hPSCs) in regenerative medicine, but transgenic modification poses safety risks such as deleterious mutagenesis. We describe here an alternative method of delivering suicide-inducing molecules explicitly to hPSCs using virus-like particles (VLPs) and demonstrate its use in eliminating undifferentiated hPSCs in vitro. VLPs were engineered from Q beta bacteriophage capsids to contain enhanced green fluorescent protein (EGFP) or cytosine deaminase (CD) and to simultaneously display multiple IgG-binding ZZ domains. After labeling with antibodies against the hPSC-specific surface glycan SSEA-S, EGFP-containing particles were shown to specifically bind undifferentiated cells in culture, and CD-containing particles were able to eliminate undifferentiated hPSCs with virtually no cytotoxicity to differentiated cells upon treatment with the prodrug 5-fluorocytosine.
引用
收藏
页码:2329 / 2338
页数:10
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