Naive Pluripotent Stem Cells Derived Directly from Isolated Cells of the Human Inner Cell Mass
Author(s) -
Ge Guo,
Ferdinand von Meyenn,
Fátima Santos,
Yaoyao Chen,
Wolf Reik,
Paul Bertone,
Austin Smith,
Jennifer Nichols
Publication year - 2016
Publication title -
stem cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.207
H-Index - 76
ISSN - 2213-6711
DOI - 10.1016/j.stemcr.2016.02.005
Subject(s) - biology , epiblast , embryonic stem cell , stem cell , microbiology and biotechnology , rex1 , inner cell mass , induced pluripotent stem cell , somatic cell , kosr , cellular differentiation , homeobox protein nanog , cell potency , genetics , blastocyst , embryo , gene , embryogenesis , gastrulation
Conventional generation of stem cells from human blastocysts produces a developmentally advanced, or primed, stage of pluripotency. In vitro resetting to a more naive phenotype has been reported. However, whether the reset culture conditions of selective kinase inhibition can enable capture of naive epiblast cells directly from the embryo has not been determined. Here, we show that in these specific conditions individual inner cell mass cells grow into colonies that may then be expanded over multiple passages while retaining a diploid karyotype and naive properties. The cells express hallmark naive pluripotency factors and additionally display features of mitochondrial respiration, global gene expression, and genome-wide hypomethylation distinct from primed cells. They transition through primed pluripotency into somatic lineage differentiation. Collectively these attributes suggest classification as human naive embryonic stem cells. Human counterparts of canonical mouse embryonic stem cells would argue for conservation in the phased progression of pluripotency in mammals.
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