重编程
诱导多能干细胞
KLF4公司
SOX2
生物
胚胎干细胞
细胞生物学
体细胞
干细胞
组蛋白脱乙酰酶抑制剂
表观遗传学
异位表达
癌症研究
细胞
遗传学
组蛋白脱乙酰基酶
细胞培养
组蛋白
基因
作者
Danwei Huangfu,Kenji Osafune,René Maehr,Wenjun Guo,Astrid Eijkelenboom,Shuibing Chen,Whitney E. Muhlestein,Douglas A. Melton
摘要
Ectopic expression of defined sets of genetic factors can reprogram somatic cells to induced pluripotent stem (iPS) cells that closely resemble embryonic stem (ES) cells. The low efficiency with which iPS cells are derived hinders studies on the molecular mechanism of reprogramming, and integration of viral transgenes, in particular the oncogenes c-Myc and Klf4, may handicap this method for human therapeutic applications. Here we report that valproic acid (VPA), a histone deacetylase inhibitor, enables reprogramming of primary human fibroblasts with only two factors, Oct4 and Sox2, without the need for the oncogenes c-Myc or Klf4. The two factor-induced human iPS cells resemble human ES cells in pluripotency, global gene expression profiles and epigenetic states. These results support the possibility of reprogramming through purely chemical means, which would make therapeutic use of reprogrammed cells safer and more practical.
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