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PLoS One. 2015 Apr 7;10(4):e0122493. doi: 10.1371/journal.pone.0122493. eCollection 2015.

Transcriptional profiling of ectoderm specification to keratinocyte fate in human embryonic stem cells.

Author information

1
Yale University, Department of Molecular, Cell and Developmental Biology, New Haven, CT, 06511, United States of America.
2
Yale University, Department of Biostatistics, Yale School of Public Health, New Haven, CT, 06520, United States of America.
3
Yale University, Yale Stem Cell Center, Genomics Facility, New Haven, CT, 06520, United States of America.

Abstract

In recent years, several studies have shed light into the processes that regulate epidermal specification and homeostasis. We previously showed that a broad-spectrum γ-secretase inhibitor DAPT promoted early keratinocyte specification in human embryonic stem cells triggered to undergo ectoderm specification. Here, we show that DAPT accelerates human embryonic stem cell differentiation and induces expression of the ectoderm protein AP2. Furthermore, we utilize RNA sequencing to identify several candidate regulators of ectoderm specification including those involved in epithelial and epidermal development in human embryonic stem cells. Genes associated with transcriptional regulation and growth factor activity are significantly enriched upon DAPT treatment during specification of human embryonic stem cells to the ectoderm lineage. The human ectoderm cell signature identified in this study contains several genes expressed in ectodermal and epithelial tissues. Importantly, these genes are also associated with skin disorders and ectodermal defects, providing a platform for understanding the biology of human epidermal keratinocyte development under diseased and homeostatic conditions.

PMID:
25849374
PMCID:
PMC4388500
DOI:
10.1371/journal.pone.0122493
[Indexed for MEDLINE]
Free PMC Article
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