Title

Sequential expression of pluripotency markers during direct reprogramming of mouse somatic cells

UMMS Affiliation

Graduate School of Biomedical Sciences; Whitehead Institute for Biomedical Research; Department of Cell Biology

Date

3-29-2008

Document Type

Article

Medical Subject Headings

Animals; 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

Disciplines

Life Sciences | Medicine and Health Sciences

Abstract

Pluripotency 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.

Rights and Permissions

Citation: Cell Stem Cell. 2008 Feb 7;2(2):151-9. Link to article on publisher's site

Related Resources

Link to Article in PubMed