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Human stem cells from single blastomeres reveal pathways of Embryonic or trophoblast fate specification
Author(s) -
Tamara Zdravkovic,
Kristopher L. Nazor,
Nicholas Larocque,
Matthew Gormley,
Matthew Donne,
Nathan Hunkapillar,
G. Giritharan,
Harold S. Bernstein,
Grace Wei,
Matthias Hebrok,
Xianmin Zeng,
Olga Genbačev,
Aras N. Mattis,
Michael McMaster,
Ana Krtolica,
Diana Valbuena,
Carlos Simón,
Louise C. Laurent,
Jeanne F. Loring,
Susan J. Fisher
Publication year - 2015
Publication title -
development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.15
H-Index - 36
eISSN - 1477-9129
pISSN - 0950-1991
DOI - 10.1242/dev.122846
Subject(s) - biology , brachyury , embryonic stem cell , embryo , blastomere , microbiology and biotechnology , trophoblast , blastocyst , stem cell , genetics , cell fate determination , embryogenesis , gene , transcription factor , placenta , fetus , mesoderm , pregnancy
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 8- to 10-cell human embryos. The UCSFB lines formed derivatives of the three germ layers and CDX2-positive 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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