Efficient Reprogramming of Human Cord Blood CD34+ Cells Into Induced Pluripotent Stem Cells With OCT4 and SOX2 Alone

被引:68
作者
Meng, Xianmei [1 ]
Neises, Amanda [1 ]
Su, Rui-Jun [2 ,3 ]
Payne, Kimberly J. [2 ,3 ]
Ritter, Linda [4 ]
Gridley, Daila S. [4 ]
Wang, Jun [5 ]
Sheng, Matilda [1 ]
Lau, K-H William [6 ]
Baylink, David J. [1 ]
Zhang, Xiao-Bing [1 ]
机构
[1] Loma Linda Univ, Dept Med, Div Regenerat Med MC1528B, Loma Linda, CA 92350 USA
[2] Loma Linda Univ, Div Anat, Dept Basic Sci, Loma Linda, CA 92350 USA
[3] Loma Linda Univ, Ctr Hlth Dispar & Mol Med, Loma Linda, CA 92350 USA
[4] Loma Linda Univ, Dept Radiat Med, Loma Linda, CA 92350 USA
[5] Loma Linda Univ, Dept Pathol, Loma Linda, CA 92350 USA
[6] Jerry L Pettis Mem VA Med Ctr, Musculoskeletal Dis Ctr, Loma Linda, CA USA
基金
美国国家科学基金会;
关键词
HUMAN SOMATIC-CELLS; GENE-EXPRESSION; LENTIVIRAL VECTORS; HUMAN FIBROBLASTS; HIV VECTORS; IPS CELLS; GENERATION; DIFFERENTIATION; TRANSFORMATION; DERIVATION;
D O I
10.1038/mt.2011.258
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The reprogramming of cord blood (CB) cells into induced pluripotent stem cells (iPSCs) has potential applications in regenerative medicine by converting CB banks into iPSC banks for allogeneic cell replacement therapy. Therefore, further investigation into novel approaches for efficient reprogramming is necessary. Here, we show that the lentiviral expression of OCT4 together with SOX2 (OS) driven by a strong spleen focus-forming virus (SFFV) promoter in a single vector can convert 2% of CB CD34(+) cells into iPSCs without additional reprogramming factors. Reprogramming efficiency was found to be critically dependent upon expression levels of OS. To generate transgene-free iPSCs, we developed an improved episomal vector with a woodchuck post-transcriptional regulatory element (Wpre) that increases transgene expression by 50%. With this vector, we successfully generated transgene-free iPSCs using OS alone. In conclusion, high-level expression of OS alone is sufficient for efficient reprogramming of CB CD34(+) cells into iPSCs. This report is the first to describe the generation of transgene-free iPSCs with the use of OCT4 and SOX2 alone. These findings have important implications for the clinical applications of iPSCs.
引用
收藏
页码:408 / 416
页数:9
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