NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE9709 Query DataSets for GSE9709
Status Public on Mar 16, 2008
Title Human induced pluripotent stem (iPS) cells from neonatal skin derived cells
Organism Homo sapiens
Experiment type Expression profiling by array
Summary Induction of germline-competent pluripotent stem cells from mouse fibroblasts has been achieved by the ectopic expression of four genes (Oct3/4, Sox2, c-Myc and Klf4). If this method can be applied to humans for the generation of personalized human pluripotent stem cells, it would greatly facilitate the therapeutic application of stem cells by avoiding the problem of immune rejection by the recipient associated with allograft transplants. Here we show that the ectopic expression of the same four genes in human neonatal skin derived cells is sufficient to induce pluripotent stem cells indistinguishable from human embryonic stem cells in morphology, gene expression, DNA methylation, teratoma formation and long term self-renewal ability. Extensive analysis of colonies generated by ectopic expression of these four genes indicates the presence of considerable heterogeneity in the induced colonies. These results provide a new finding to generate human induced pluripotent stem cells from postnatal somatic tissues.
Keywords: Cell type comparison
 
Overall design The microarray study was carried out using Affymetrix Human Genome U133 Plus 2.0 gene expression arrays or Agilent Whole Human Genome Oligo microarrays. Total RNA was extracted from cells with RNeasy (Qiagen). For Affymetrix array, biotin-labelled cRNA was reverse transcribed from 1 µg of total RNA according to Affymetrix technical protocols. Fifteen micrograms of cRNA was fragmented and hybridized to Affymetrix U133 plus 2 GeneChip arrays at 45C for 16 h and then washed and stained using Affimetrix Fluidics. The arrays were scanned using an Affimetrix GCS3000 scanner, and the images obtained were processed to data using the GCOS software. For Agilent array (G4112A), Total RNA was labeled with Cy3. Samples were hybridized with Agilent Gene Expression Hybridization kit according to the one color protocol. Arrays were scanned with a Agilent Microarray Scanner System and processed to data with Feature Extraction Software (v.9.5.3). Data from this experiment and the GEO database were analysed with the GeneSpring 7.3.1. software.
 
Contributor(s) Masaki H, Ishikawa T, Takahashi S, Sakurada K
Citation(s) 19383391
Submission date Nov 28, 2007
Last update date Mar 25, 2019
Contact name Tetsuya Ishikawa
E-mail(s) [email protected]
Phone +81-3-3542-2511
Fax +81-3-5565-0727
Organization name Japanease National Cancer Center
Department Research Institute
Lab Section for Studies on Metastasis
Street address 1-1, Tsukiji 5-chome
City Chuo-ku
State/province Tokyo
ZIP/Postal code 104-0045
Country Japan
 
Platforms (2)
GPL570 [HG-U133_Plus_2] Affymetrix Human Genome U133 Plus 2.0 Array
GPL1708 Agilent-012391 Whole Human Genome Oligo Microarray G4112A (Feature Number version)
Samples (13)
GSM245339 Human induced pluripotent stem cell clone 1-8 cultured in mTeSR1 on Matrigel (2)
GSM245341 Human neonatal dermal fibroblast (5F0438)
GSM245342 Human induced pluripotent stem cell clone 1-8 cultured in MEF-conditioned medium on Matrigel
Relations
BioProject PRJNA103613

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE9709_RAW.tar 74.1 Mb (http)(custom) TAR (of CEL, TXT)
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap