Klf4 reverts developmentally programmed restriction of ground state pluripotency
Wellcome/MRC Cambridge Stem Cell Institute · University of Cambridge · +1 more institution
Abstract
Mouse embryonic stem (ES) cells derived from pluripotent early epiblast contribute functionally differentiated progeny to all foetal lineages of chimaeras. By contrast, epistem cell (EpiSC) lines from post-implantation epithelialised epiblast are unable to colonise the embryo even though they express the core pluripotency genes Oct4, Sox2 and Nanog. We examined interconversion between these two cell types. ES cells can readily become EpiSCs in response to growth factor cues. By contrast, EpiSCs do not change into ES cells. We exploited PiggyBac transposition to introduce a single reprogramming factor, Klf4, into EpiSCs. No effect was apparent in EpiSC culture conditions, but in ground state ES cell conditions…
Citation impact
- FWCI
- 31.48
- Percentile
- 100%
- References
- 36
Authors
7- GGGe GuoCorresponding
Wellcome/MRC Cambridge Stem Cell Institute, University of Cambridge, Bridge University
- JYJian Yang
Wellcome/MRC Cambridge Stem Cell Institute, University of Cambridge, Bridge University
- JNJennifer Nichols
Wellcome/MRC Cambridge Stem Cell Institute, University of Cambridge
- JHJohn Hall
Wellcome/MRC Cambridge Stem Cell Institute, University of Cambridge, Bridge University
- IEIsobel Eyres
Wellcome/MRC Cambridge Stem Cell Institute, University of Cambridge
Topics & keywords
- Biology
- Epiblast
- Reprogramming
- KLF4
- SOX2
- Induced pluripotent stem cell
- Homeobox protein NANOG
- Embryonic stem cell