Reprogramming of human somatic cells to pluripotency with defined factors.

TitleReprogramming of human somatic cells to pluripotency with defined factors.
Publication TypeJournal Article
Year of Publication2008
AuthorsPark I-H, Zhao R, West JA, Yabuuchi A, Huo H, Ince TA, Lerou PH, M Lensch W, Daley GQ
JournalNature
Volume451
Issue7175
Pagination141-6
Date Published2008 Jan 10
ISSN1476-4687
KeywordsAdult, Animals, Cell Differentiation, Cell Shape, Cells, Cultured, DNA Methylation, DNA-Binding Proteins, Embryonic Stem Cells, Fetus, Fibroblasts, Gene Expression Profiling, HMGB Proteins, Homeodomain Proteins, Humans, Infant, Newborn, Kruppel-Like Transcription Factors, Mice, Nanog Homeobox Protein, Octamer Transcription Factor-3, Pluripotent Stem Cells, Promoter Regions, Genetic, Proto-Oncogene Proteins c-myc, SOXB1 Transcription Factors, Teratoma, Transcription Factors, Transplantation, Heterologous
Abstract

Pluripotency pertains to the cells of early embryos that can generate all of the tissues in the organism. Embryonic stem cells are embryo-derived cell lines that retain pluripotency and represent invaluable tools for research into the mechanisms of tissue formation. Recently, murine fibroblasts have been reprogrammed directly to pluripotency by ectopic expression of four transcription factors (Oct4, Sox2, Klf4 and Myc) to yield induced pluripotent stem (iPS) cells. Using these same factors, we have derived iPS cells from fetal, neonatal and adult human primary cells, including dermal fibroblasts isolated from a skin biopsy of a healthy research subject. Human iPS cells resemble embryonic stem cells in morphology and gene expression and in the capacity to form teratomas in immune-deficient mice. These data demonstrate that defined factors can reprogramme human cells to pluripotency, and establish a method whereby patient-specific cells might be established in culture.

DOI10.1038/nature06534
Alternate JournalNature
PubMed ID18157115
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Tan Ince, M.D., Ph.D.

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