| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 2093437 | Stem Cell Reports | 2016 | 9 Pages |
•OSKM induce extraembryonic endoderm stem cells (iXENCs) in mouse fibroblasts•iPSCs do not transition through an iXEN intermediate•iXENCs are derived from fibroblasts in parallel to iPSCs•Endodermal genes regulate the choice to become iXENCs or iPSCs
SummaryThe reprogramming factors OCT4, SOX2, KLF4, and MYC (OSKM) can reactivate the pluripotency network in terminally differentiated cells, but also regulate expression of non-pluripotency genes in other contexts, such as the mouse primitive endoderm. The primitive endoderm is an extraembryonic lineage established in parallel to the pluripotent epiblast in the blastocyst, and is the progenitor pool for extraembryonic endoderm stem (XEN) cells. We show that OSKM induce expression of endodermal genes, leading to formation of induced XEN (iXEN) cells, which possess key properties of blastocyst-derived XEN cells, including morphology, transcription profile, self-renewal, and multipotency. Our data show that iXEN cells arise in parallel to induced pluripotent stem cells, indicating that OSKM drive cells to two distinct cell fates during reprogramming.
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