| Literature DB >> 23117585 |
Barbara S Mallon1, Josh G Chenoweth, Kory R Johnson, Rebecca S Hamilton, Paul J Tesar, Amarendra S Yavatkar, Leonard J Tyson, Kyeyoon Park, Kevin G Chen, Yang C Fann, Ronald D G McKay.
Abstract
Much of the excitement generated by induced pluripotent stem cell technology is concerned with the possibility of disease modeling as well as the potential for personalized cell therapy. However, to pursue this it is important to understand the 'normal' pluripotent state including its inherent variability. We have performed various molecular profiling assays for 21 hESC lines and 8 hiPSC lines to generate a comprehensive snapshot of the undifferentiated state of pluripotent stem cells. Analysis of the gene expression data revealed no iPSC-specific gene expression pattern in accordance with previous reports. We further compared cells, differentiated as embryoid bodies in 2 media proposed to initiate differentiation towards separate cell fates, as well as 20 adult tissues. From this analysis we have generated a gene list which defines pluripotency and establishes a baseline for the pluripotent state. Finally, we provide lists of genes enriched under both differentiation conditions which show the proposed bias toward independent cell fates. Published by Elsevier B.V.Entities:
Mesh:
Year: 2012 PMID: 23117585 PMCID: PMC3590800 DOI: 10.1016/j.scr.2012.09.002
Source DB: PubMed Journal: Stem Cell Res ISSN: 1873-5061 Impact factor: 2.020