Author(s): KarwackiNeisius V, Gke J, Osorno R, Halbritter F, Ng JH, , KarwackiNeisius V, Gke J, Osorno R, Halbritter F, Ng JH, , KarwackiNeisius V, Gke J, Osorno R, Halbritter F, Ng JH, , KarwackiNeisius V, Gke J, Osorno R, Halbritter F, Ng JH,
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Abstract Embryonic stem cell (ESC) pluripotency is governed by a gene regulatory network centered on the transcription factors Oct4 and Nanog. To date, robust self-renewing ESC states have only been obtained through the chemical inhibition of signaling pathways or enforced transgene expression. Here, we show that ESCs with reduced Oct4 expression resulting from heterozygosity also exhibit a stabilized pluripotent state. Despite having reduced Oct4 expression, Oct4(+/-) ESCs show increased genome-wide binding of Oct4, particularly at pluripotency-associated enhancers, homogeneous expression of pluripotency transcription factors, enhanced self-renewal efficiency, and delayed differentiation kinetics. Cells also exhibit increased Wnt expression, enhanced leukemia inhibitory factor (LIF) sensitivity, and reduced responsiveness to fibroblast growth factor. Although they are able to maintain pluripotency in the absence of bone morphogenetic protein, removal of LIF destabilizes pluripotency. Our findings suggest that cells with a reduced Oct4 concentration range are maintained in a robust pluripotent state and that the wild-type Oct4 concentration range enables effective differentiation. Copyright © 2013 Elsevier Inc. All rights reserved.
This article was published in Cell Stem Cell
and referenced in Journal of Cell Signaling