
Somatic cell nuclear transfer allows trans-acting factors present in the mammalian oocyte to reprogram somatic cell nuclei to an undifferentiated state. We show that four factors ( OCT4, SOX2, NANOG , and LIN28 ) are sufficient to reprogram human somatic cells to pluripotent stem cells that exhibit the essential characteristics of embryonic stem (ES) cells. These induced pluripotent human stem cells have normal karyotypes, express telomerase activity, express cell surface markers and genes that characterize human ES cells, and maintain the developmental potential to differentiate into advanced derivatives of all three primary germ layers. Such induced pluripotent human cell lines should be useful in the production of new disease models and in drug development, as well as for applications in transplantation medicine, once technical limitations (for example, mutation through viral integration) are eliminated.
Homeodomain Proteins, Infant, Newborn, Cell Differentiation, Mice, SCID, Nanog Homeobox Protein, Fibroblasts, Cellular Reprogramming, Cell Line, DNA-Binding Proteins, Mice, Fetus, HMGB Proteins, Karyotyping, Animals, Humans, Cell Shape, Octamer Transcription Factor-3, Embryonic Stem Cells, Cell Proliferation, Oligonucleotide Array Sequence Analysis
Homeodomain Proteins, Infant, Newborn, Cell Differentiation, Mice, SCID, Nanog Homeobox Protein, Fibroblasts, Cellular Reprogramming, Cell Line, DNA-Binding Proteins, Mice, Fetus, HMGB Proteins, Karyotyping, Animals, Humans, Cell Shape, Octamer Transcription Factor-3, Embryonic Stem Cells, Cell Proliferation, Oligonucleotide Array Sequence Analysis
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