Abstract
Induced pluripotent stem (iPS) cells have been generated from mouse and human somatic cells by introducing Oct3/4 and Sox2 with either Klf4 and c-Myc or Nanog and Lin28 using retroviruses or lentiviruses. Patient-specific iPS cells could be useful in drug discovery and regenerative medicine. However, viral integration into the host genome increases the risk of tumorigenicity. Here, we report the generation of mouse iPS cells without viral vectors. Repeated transfection of two expression plasmids, one containing the complementary DNAs (cDNAs) of Oct3/4, Sox2, and Klf4 and the other containing the c-Myc cDNA, into mouse embryonic fibroblasts resulted in iPS cells without evidence of plasmid integration, which produced teratomas when transplanted into mice and contributed to adult chimeras. The production of virus-free iPS cells, albeit from embryonic fibroblasts, addresses a critical safety concern for potential use of iPS cells in regenerative medicine.
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Animals
-
Cellular Reprogramming*
-
Chimera
-
DNA, Complementary
-
Embryo, Mammalian / cytology
-
Embryonic Stem Cells / cytology
-
Embryonic Stem Cells / metabolism
-
Fibroblasts / cytology*
-
Fibroblasts / metabolism
-
Genes, myc
-
Genetic Vectors
-
Kruppel-Like Factor 4
-
Kruppel-Like Transcription Factors / genetics
-
Kruppel-Like Transcription Factors / metabolism
-
Mice
-
Octamer Transcription Factor-3 / genetics
-
Octamer Transcription Factor-3 / metabolism
-
Plasmids*
-
Pluripotent Stem Cells* / cytology
-
Pluripotent Stem Cells* / metabolism
-
Pluripotent Stem Cells* / transplantation
-
Retroviridae / genetics
-
SOXB1 Transcription Factors / genetics
-
SOXB1 Transcription Factors / metabolism
-
Teratoma / etiology
-
Transfection*
Substances
-
DNA, Complementary
-
KLF4 protein, human
-
Klf4 protein, mouse
-
Kruppel-Like Factor 4
-
Kruppel-Like Transcription Factors
-
Octamer Transcription Factor-3
-
Pou5f1 protein, mouse
-
SOXB1 Transcription Factors
-
Sox2 protein, mouse