Cardiac Engraftment of Genetically-Selected Parthenogenetic Stem Cell-Derived Cardiomyocytes

被引:3
|
作者
Yang, Tao [1 ,2 ]
Rubart, Michael [2 ,3 ]
Soonpaa, Mark H. [2 ,3 ]
Didie, Michael [4 ,5 ]
Christalla, Peter [4 ,5 ]
Zimmermann, Wolfram-Hubertus [4 ,5 ]
Field, Loren J. [2 ,3 ]
机构
[1] Tongji Univ, Res Ctr Translat Med, Shanghai East Hosp, Sch Med, Shanghai 200092, Peoples R China
[2] Indiana Univ, Riley Heart Res Ctr, Herman B Wells Ctr Pediat Res, Sch Med, Indianapolis, IN 46204 USA
[3] Indiana Univ, Krannert Inst Cardiol, Sch Med, Indianapolis, IN 46204 USA
[4] Univ Med Ctr Gottingen, Inst Pharmacol, Gottingen, Germany
[5] DZHK German Ctr Cardiovasc Res, Gottingen, Germany
来源
PLOS ONE | 2015年 / 10卷 / 06期
基金
中国国家自然科学基金;
关键词
INFARCTED RAT HEARTS; MYOCARDIUM; GRAFTS; PROLIFERATION; SHEETS; REPAIR; MICE;
D O I
10.1371/journal.pone.0131511
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Parthenogenetic stem cells (PSCs) are a promising candidate donor for cell therapy applications. Similar to embryonic stem cells (ESCs) and induced pluripotent stem cells (iPSCs), PSCs exhibit self-renewing capacity and clonogenic proliferation in vitro. PSCs exhibit largely haploidentical genotype, and as such may constitute an attractive population for allogenic applications. In this study, PSCs isolated from transgenic mice carrying a cardiomyocyte-restricted reporter transgene to permit tracking of donor cells were genetically modified to carry a cardiomyocyte-restricted aminoglycoside phosphotransferase expression cassette (MHC-neor/pGK-hygror) to permit the generation of highly enriched cardiomyocyte cultures from spontaneously differentiating PSCs by simple selection with the neomycin analogue G148. Following engraftment into isogenic recipient hearts, the selected cardiomyocytes formed a functional syncytium with the host myocardium as evidenced by the presence of entrained intracellular calcium transients. These cells thus constitute a potential source of therapeutic donor cells.
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页数:12
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