| Literature DB >> 28494860 |
Ursula Nosi1, Fredrik Lanner2, Tsu Huang1, Brian Cox3.
Abstract
The first cell fate choice of the preimplantation embryo generates the extraembryonic trophoblast and embryonic epiblast lineages. Embryonic stem cells (ESCs) and trophoblast stem cells (TSCs) can be utilized to investigate molecular mechanisms of this first cell fate decision. It has been established that ESCs can be induced to acquire trophoblast lineage characteristics upon manipulation of lineage-determining transcription factors. Here, we have interrogated the potential of microRNAs (miRNAs) to drive trans-differentiation of ESCs into the trophoblast lineage. Analysis of gene expression data identified a network of TSC-enriched miRNAs that were predicted to target mRNAs enriched in ESCs. Ectopic expression of these miRNAs in ESCs resulted in a stable trophoblast phenotype, supported by gene expression changes and in vivo contribution potential. This process is highly miRNA-specific and dependent on Hdac2 inhibition. Our experimental evidence suggests that these miRNAs promote a mural trophectoderm (TE)-like cell fate with physiological properties that differentiate them from the polar TE.Entities:
Keywords: cell fate; embryo; embryonic stem cell; epigenetics; microRNA; microarray; mouse; reprogramming; trophectoderm; trophoblast stem cell
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Year: 2017 PMID: 28494860 DOI: 10.1016/j.celrep.2017.04.040
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423