Dev122846 4010..4025

نویسندگان

  • Tamara Zdravkovic
  • Kristopher L. Nazor
  • Nicholas Larocque
  • Matthew Gormley
  • Matthew Donne
  • Nathan Hunkapillar
  • Matthias Hebrok
  • Xianmin Zeng
  • Olga Genbacev
  • Aras Mattis
  • Michael T. McMaster
  • Ana Krtolica
  • Diana Valbuena
  • Carlos Simón
  • Louise C. Laurent
  • Jeanne F. Loring
  • Susan J. Fisher
چکیده

Mechanisms of initial cell fate decisions differ among species. To gain insights into lineage allocation in humans, we derived ten human embryonic stem cell lines (designated UCSFB1-10) from single blastomeres of four 8-cell embryos and one 12-cell embryo from a single couple. Compared with numerous conventional lines from blastocysts, they had unique gene expression and DNA methylation patterns that were, in part, indicative of trophoblast competence. At a transcriptional level, UCSFB lines from different embryos were often more closely related than those from the same embryo. As predicted by the transcriptomic data, immunolocalization of EOMES, T brachyury, GDF15 and active β-catenin revealed differential expression among blastomeres of 8to 10-cell human embryos. The UCSFB lines formed derivatives of the three germ layers and CDX2positive progeny, from which we derived the first human trophoblast stem cell line. Our data suggest heterogeneity among early-stage blastomeres and that the UCSFB lines have unique properties, indicative of a more immature state than conventional lines.

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تاریخ انتشار 2015