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Species-specific developmental timing is maintained by pluripotent stem cells ex utero.
Barry, Christopher; Schmitz, Matthew T; Jiang, Peng; Schwartz, Michael P; Duffin, Bret M; Swanson, Scott; Bacher, Rhonda; Bolin, Jennifer M; Elwell, Angela L; McIntosh, Brian E; Stewart, Ron; Thomson, James A.
Afiliação
  • Barry C; Morgridge Institute for Research, Madison, WI 53715, USA.
  • Schmitz MT; Morgridge Institute for Research, Madison, WI 53715, USA.
  • Jiang P; Morgridge Institute for Research, Madison, WI 53715, USA.
  • Schwartz MP; Center for Sustainable Nanotechnology, Department of Chemistry, University of Wisconsin-Madison, WI 53706, USA.
  • Duffin BM; Morgridge Institute for Research, Madison, WI 53715, USA.
  • Swanson S; Morgridge Institute for Research, Madison, WI 53715, USA.
  • Bacher R; Department of Statistics, University of Wisconsin-Madison, WI 53706, USA.
  • Bolin JM; Morgridge Institute for Research, Madison, WI 53715, USA.
  • Elwell AL; Morgridge Institute for Research, Madison, WI 53715, USA.
  • McIntosh BE; Morgridge Institute for Research, Madison, WI 53715, USA.
  • Stewart R; Morgridge Institute for Research, Madison, WI 53715, USA.
  • Thomson JA; Morgridge Institute for Research, Madison, WI 53715, USA; Department of Cell and Regenerative Biology, University of Wisconsin School of Medicine and Public Health, Madison, WI 53706, USA; Department of Molecular, Cellular, and Developmental Biology, University of California, Santa Barbara, CA 93106
Dev Biol ; 423(2): 101-110, 2017 03 15.
Article em En | MEDLINE | ID: mdl-28179190
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Células-Tronco Pluripotentes Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Células-Tronco Pluripotentes Idioma: En Ano de publicação: 2017 Tipo de documento: Article