Sequential expression of pluripotency markers during direct reprogramming of mouse somatic cells
Foreman, Ruth K.
Welstead, G. Grant
Lengner, Christopher Joachim
UMass Chan AffiliationsDepartment of Cell Biology
Whitehead Institute for Biomedical Research
Graduate School of Biomedical Sciences
Document TypeJournal Article
KeywordsAnimals; Biological Markers; Cell Differentiation; Cell Line; Epigenesis, Genetic; Fibroblasts; Gene Expression Regulation, Viral; Genetic Vectors; Humans; Lentivirus; Mice; Nuclear Reprogramming; Pluripotent Stem Cells; Transcription Factors
Medicine and Health Sciences
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AbstractPluripotency can be induced in differentiated murine and human cells by retroviral transduction of Oct4, Sox2, Klf4, and c-Myc. We have devised a reprogramming strategy in which these four transcription factors are expressed from doxycycline (dox)-inducible lentiviral vectors. Using these inducible constructs, we derived induced pluripotent stem (iPS) cells from mouse embryonic fibroblasts (MEFs) and found that transgene silencing is a prerequisite for normal cell differentiation. We have analyzed the timing of known pluripotency marker activation during mouse iPS cell derivation and observed that alkaline phosphatase (AP) was activated first, followed by stage-specific embryonic antigen 1 (SSEA1). Expression of Nanog and the endogenous Oct4 gene, marking fully reprogrammed cells, was only observed late in the process. Importantly, the virally transduced cDNAs needed to be expressed for at least 12 days in order to generate iPS cells. Our results are a step toward understanding some of the molecular events governing epigenetic reprogramming.
SourceCell Stem Cell. 2008 Feb 7;2(2):151-9. Link to article on publisher's site
Permanent Link to this Itemhttp://hdl.handle.net/20.500.14038/32921
Related ResourcesLink to Article in PubMed