Reprogramming Cellular Identity for Regenerative Medicine

被引:148
作者
Cherry, Anne B. C. [1 ,2 ,3 ,4 ,5 ,6 ]
Daley, George Q. [1 ,2 ,3 ,4 ,5 ,6 ]
机构
[1] Childrens Hosp Boston, Howard Hughes Med Inst, Manton Ctr Orphan Dis Res, Div Pediat Hematol Oncol,Stem Cell Transplantat P, Boston, MA 02115 USA
[2] Dana Farber Canc Inst, Boston, MA 02115 USA
[3] Brigham & Womens Hosp, Div Hematol, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
[5] Broad Inst, Cambridge, MA 02142 USA
[6] Harvard Stem Cell Inst, Cambridge, MA 02138 USA
关键词
PLURIPOTENT STEM-CELLS; IPS CELLS; PARKINSONS-DISEASE; GENETIC CORRECTION; DNA METHYLATION; PATIENT; ADULT; FIBROBLASTS; DIFFERENTIATION; GENERATION;
D O I
10.1016/j.cell.2012.02.031
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
Although development leads unidirectionally toward more restricted cell fates, recent work in cellular reprogramming has proven that one cellular identity can strikingly convert into another, promising countless applications in biomedical research and paving the way for modeling diseases with patient-derived stem cells. To date, there has been little discussion of which disease models are likely to be most informative. Here, we review evidence demonstrating that, because environmental influences and epigenetic signatures are largely erased during reprogramming, patient-specific models of diseases with strong genetic bases and high penetrance are likely to prove most informative in the near term. We also discuss the implications of the new reprogramming paradigm in biomedicine and outline how reprogramming of cell identities is enhancing our understanding of cell differentiation and prospects for cellular therapies and in vivo regeneration.
引用
收藏
页码:1110 / 1122
页数:13
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