Species-specific developmental timing is maintained by pluripotent stem cells ex utero

Dev Biol. 2017 Mar 15;423(2):101-110. doi: 10.1016/j.ydbio.2017.02.002. Epub 2017 Feb 6.

Abstract

How species-specific developmental timing is controlled is largely unknown. By following human embryonic stem (ES) cell and mouse epiblast stem (EpiS) cell differentiation through detailed RNA-sequencing time courses, here we show that pluripotent stem cells closely retain in vivo species-specific developmental timing in vitro. In identical neural differentiation conditions in vitro, gene expression profiles are accelerated in mouse EpiS cells compared to human ES cells with relative rates of differentiation closely reflecting the rates of progression through the Carnegie stages in utero. Dynamic Time Warping analysis identified 3389 genes that were regulated more quickly in mouse EpiS cells and identified none that were regulated more quickly in human ES cells. Interestingly, we also find that human ES cells differentiated in teratomas maintain the same rate of differentiation observed in vitro in spite of being grown in a mouse host. These results suggest the existence of a cell autonomous, species-specific developmental clock that pluripotent stem cells maintain even out of context of an intact embryo.

Keywords: Brain development; Developmental time; Differentiation; Embryonic stem cells.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Cell Differentiation / genetics
  • Cell Line
  • Embryonic Stem Cells / cytology
  • Female
  • Gene Expression Profiling
  • Gene Expression Regulation
  • Humans
  • Mice, SCID
  • Neurons / cytology
  • Pluripotent Stem Cells / cytology*
  • Pluripotent Stem Cells / metabolism*
  • Species Specificity
  • Teratoma / pathology
  • Time Factors