Tracking the embryonic stem cell transition from ground state pluripotency

Development. 2017 Apr 1;144(7):1221-1234. doi: 10.1242/dev.142711. Epub 2017 Feb 7.

Abstract

Mouse embryonic stem (ES) cells are locked into self-renewal by shielding from inductive cues. Release from this ground state in minimal conditions offers a system for delineating developmental progression from naïve pluripotency. Here, we examine the initial transition process. The ES cell population behaves asynchronously. We therefore exploited a short-half-life Rex1::GFP reporter to isolate cells either side of exit from naïve status. Extinction of ES cell identity in single cells is acute. It occurs only after near-complete elimination of naïve pluripotency factors, but precedes appearance of lineage specification markers. Cells newly departed from the ES cell state display features of early post-implantation epiblast and are distinct from primed epiblast. They also exhibit a genome-wide increase in DNA methylation, intermediate between early and late epiblast. These findings are consistent with the proposition that naïve cells transition to a distinct formative phase of pluripotency preparatory to lineage priming.

Keywords: ES cells; Epiblast; Methylome; Pluripotency; Rex1; Transcriptome.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Lineage
  • Cell Self Renewal
  • Cell Tracking*
  • DNA Methylation / genetics
  • Down-Regulation
  • Embryo, Mammalian / cytology
  • Embryonic Stem Cells / cytology*
  • Embryonic Stem Cells / metabolism
  • Genes, Reporter
  • Germ Layers / cytology
  • Kinetics
  • Mice
  • Pluripotent Stem Cells / cytology*
  • Pluripotent Stem Cells / metabolism
  • Stem Cell Transplantation
  • Transcription Factors / metabolism
  • Transcription, Genetic

Substances

  • Transcription Factors