Proceedings of the National Academy of Sciences · 2008 · 1K citations · 18 references
Life SciencesCell BiologyMolecular BiologyCell DifferentiationRegenerative MedicineStem Cell BiologyCellular ReprogrammingEmbryonic Stem CellsPluripotent Stem CellsSomatic Cell Nuclear TransferStem Cell DifferentiationStem Cell ReprogrammingHuman Embryonic Stem CellsHuman Induced Pluripotent Stem Cell ModelsInduced Pluripotent Stem Cell DifferentiationInduced Pluripotent Stem Cell ModelsInduced Pluripotent Stem Cell ReprogrammingInduced Pluripotent Stem CellsPluripotency InductionPluripotent Stem Cell Differentiation
Human iPS cells can accelerate clinical treatment of degenerative diseases, but current nuclear transfer and cell‑fusion methods face clinical barriers. The authors aim to generate patient‑specific iPS cells from dermal fibroblasts by ectopic expression of KLF4, OCT4, SOX2, and C‑MYC. They achieve this by transducing fibroblasts with these defined transcription factors to reprogram them into iPS cells. The resulting iPS cells are morphologically and transcriptionally indistinguishable from human embryonic stem cells, retain a normal karyotype, are confirmed to originate from the donor, and can differentiate into all three germ layers, demonstrating pluripotency and supporting their therapeutic potential.
The generation of patient-specific pluripotent stem cells has the potential to accelerate the implementation of stem cells for clinical treatment of degenerative diseases. Technologies including somatic cell nuclear transfer and cell fusion might generate such cells but are hindered by issues that might prevent them from being used clinically. Here, we describe methods to use dermal fibroblasts easily obtained from an individual human to generate human induced pluripotent stem (iPS) cells by ectopic expression of the defined transcription factors KLF4, OCT4, SOX2, and C-MYC. The resultant cell lines are morphologically indistinguishable from human embryonic stem cells (HESC) generated from the inner cell mass of a human preimplantation embryo. Consistent with these observations, human iPS cells share a nearly identical gene-expression profile with two established HESC lines. Importantly, DNA fingerprinting indicates that the human iPS cells were derived from the donor material and are not a result of contamination. Karyotypic analyses demonstrate that reprogramming of human cells by defined factors does not induce, or require, chromosomal abnormalities. Finally, we provide evidence that human iPS cells can be induced to differentiate along lineages representative of the three embryonic germ layers indicating the pluripotency of these cells. Our findings are an important step toward manipulating somatic human cells to generate an unlimited supply of patient-specific pluripotent stem cells. In the future, the use of defined factors to change cell fate may be the key to routine nuclear reprogramming of human somatic cells.
18
Induction of Pluripotent Stem Cells from Adult Human Fibroblasts by Defined Factors
Kazutoshi Takahashi, Koji Tanabe, Mari Ohnuki et al. · Cell · 2007 · 20.2K citations
Induced Pluripotent Stem Cell Lines Derived from Human Somatic Cells
Junying Yu, Maxim A. Vodyanik, Kim Smuga-Otto et al. · Science · 2007 · 10.3K citations