Derivation and Long-Term Culture of Transgene-Free Human Induced Pluripotent Stem Cells on Synthetic Substrates

被引:15
作者
Villa-Diaz, Luis Gerardo [1 ,2 ]
Kim, Jin Koo [1 ,2 ]
Lahann, Ierg [2 ,3 ]
Krebsbach, Paul H. [1 ,2 ]
机构
[1] Univ Michigan, Dept Biol & Mat Sci, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Biointerfaces Inst, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Dept Chem Engn, Ann Arbor, MI 48109 USA
关键词
Induced pluripotent stem cells; Synthetic coating; Stem cells; Regenerative medicine; iPSC; Differentiation; Feeder-free culture; FEEDER-FREE CULTURE; DIRECTED DIFFERENTIATION; DEFINED CONDITIONS; POLYMER COATINGS; SENDAI-VIRUS; GROWTH; VECTOR; FIBROBLASTS; INDUCTION; SYSTEM;
D O I
10.5966/sctm.2014-0087
中图分类号
Q813 [细胞工程];
学科分类号
摘要
We describe a platform to derive, culture, and differentiate genomically stable, transgene-free human induced pluripotent stem cells (iPSCs) on a fully synthetic polymer substrate made of a grafted zwitterionic hydrogel: poly2-(methacryloyloxy)ethyl dimethyl-(3-sulfopropyl) ammonium hydroxide (PMEDSAH). Three independent transgene-free iPSC lines derived in these conditions demonstrated continuous self-renewal, genomic stability, and pluripotency in vitro and in vivo after up to 9 months of continuous in vitro culture on PMEDSAH-grafted plates. Together, these data demonstrate the strength this alternative platform offers to generate and maintain human iPSCs for regenerative medicine.
引用
收藏
页码:1410 / 1417
页数:8
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