Derivation of engraftable skeletal myoblasts from human embryonic stem cells

被引:228
作者
Barberi, Tiziano
Bradbury, Michelle
Dincer, Zehra
Panagiotakos, Georgia
Socci, Nicholas D.
Studer, Lorenz
机构
[1] Sloan Kettering Inst, Dept Radiol, New York, NY 10021 USA
[2] Sloan Kettering Inst, Computat Biol Ctr, New York, NY 10021 USA
[3] Sloan Kettering Inst, Dev Biol Program, Div Neurosurg, New York, NY 10021 USA
关键词
D O I
10.1038/nm1533
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
Human embryonic stem cells (hESCs) are a promising source for cell therapy in degenerative diseases. A key step in establishing the medical potential of hESCs is the development of techniques for the conversion of hESCs into tissue-restricted precursors suitable for transplantation. We recently described the derivation of multipotent mesenchymal precursors from hESCs. Nevertheless, our previous study was limited by the requirement for mouse feeders and the lack of in vivo data. Here we report a stroma-free induction system for deriving mesenchymal precursors. Selective culture conditions and fluorescence-activated cell sorting (FACS)-mediated purification yielded multipotent mesenchymal precursors and skeletal myoblasts. Skeletal muscle cells undergo in vitro maturation resulting in myotube formation and spontaneous twitching. We found that hESC-derived skeletal myoblasts were viable after transplantation into the tibialis anterior muscle of SCID/Beige mice, as assessed by bioluminescence imaging. Lack of teratoma formation and evidence of long-term myoblast engraftment suggests considerable potential for future therapeutic applications.
引用
收藏
页码:642 / 648
页数:7
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