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Cell Stem Cell. 2008 Mar 6;2(3):230-40. doi: 10.1016/j.stem.2008.02.001. Epub 2008 Feb 14.

Defining molecular cornerstones during fibroblast to iPS cell reprogramming in mouse.

Author information

1
Massachusetts General Hospital Cancer Center and Center for Regenerative Medicine, 185 Cambridge Street, Boston, MA 02114, USA.

Abstract

Ectopic expression of the transcription factors Oct4, Sox2, c-Myc, and Klf4 in fibroblasts generates induced pluripotent stem (iPS) cells. Little is known about the nature and sequence of molecular events accompanying nuclear reprogramming. Using doxycycline-inducible vectors, we have shown that exogenous factors are required for about 10 days, after which cells enter a self-sustaining pluripotent state. We have identified markers that define cell populations prior to and during this transition period. While downregulation of Thy1 and subsequent upregulation of SSEA-1 occur at early time points, reactivation of endogenous Oct4, Sox2, telomerase, and the silent X chromosome mark late events in the reprogramming process. Cell sorting with these markers allows for a significant enrichment of cells with the potential to become iPS cells. Our results suggest that factor-induced reprogramming is a gradual process with defined intermediate cell populations that contain the majority of cells poised to become iPS cells.

PMID:
18371448
PMCID:
PMC3538379
DOI:
10.1016/j.stem.2008.02.001
[Indexed for MEDLINE]
Free PMC Article

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