期刊
NATURE CELL BIOLOGY
卷 13, 期 3, 页码 215-U61出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/ncb2164
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资金
- NICHD
- NHLBI
- NIMH/NIH
- California Institute for Regenerative Medicine
- Prostate Cancer Foundation
- Fate Therapeutics
- Esther B. O'Keeffe Foundation
- Scripps Research Institute
Here we show that conventional reprogramming towards pluripotency through overexpression of Oct4, Sox2, Klf4 and c-Myc can be shortcut and directed towards cardiogenesis in a fast and efficient manner. With as little as 4 days of transgenic expression of these factors, mouse embryonic fibroblasts (MEFs) can be directly reprogrammed to spontaneously contracting patches of differentiated cardiomyocytes over a period of 11-12 days. Several lines of evidence suggest that a pluripotent intermediate is not involved. Our method represents a unique strategy that allows a transient, plastic developmental state established early in reprogramming to effectively function as a cellular transdifferentiation platform, the use of which could extend beyond cardiogenesis. Our study has potentially wide-ranging implications for induced pluripotent stem cell (iPSC)-factor-based reprogramming and broadens the existing paradigm.
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