Notch Signaling Is Inactive but Inducible in Human Embryonic Stem Cells
- 1 July 2006
- journal article
- Published by Oxford University Press (OUP) in The International Journal of Cell Cloning
- Vol. 24 (7), 1646-1653
- https://doi.org/10.1634/stemcells.2005-0314
Abstract
The NOTCH signaling pathway performs a wide range of critical functions in a number of different cell types during development and differentiation. The role of NOTCH signals in human embryonic stem cells (hESCs) has not been tested. We measured the activity of canonical NOTCH signaling in undifferentiated embryonic stem (ES) cells and tested the requirement for NOTCH activity in hESC self-renewal or differentiation by growing hESCs in the presence of gamma-secretase inhibitors. Our results suggest that NOTCH signaling is not required for the propagation of undifferentiated human ES cells but instead is required for the maintenance of the differentiating cell types that accumulate in human ES cell cultures. Our studies suggest that NOTCH signaling is not required in human embryonic differentiation until the formation of extraembryonic, germ layer, or tissue-specific stem cells and progenitors.Keywords
This publication has 40 references indexed in Scilit:
- TGFβ/activin/nodal signaling is necessary for the maintenance of pluripotency in human embryonic stem cellsDevelopment, 2005
- Basic Fibroblast Growth Factor Supports Undifferentiated Human Embryonic Stem Cell Growth Without Conditioned MediumThe International Journal of Cell Cloning, 2005
- Differences between human and mouse embryonic stem cellsDevelopmental Biology, 2004
- A Genome-Wide Study of Gene Activity Reveals Developmental Signaling Pathways in the Preimplantation Mouse EmbryoDevelopmental Cell, 2004
- Maintenance of pluripotency in human and mouse embryonic stem cells through activation of Wnt signaling by a pharmacological GSK-3-specific inhibitorNature Medicine, 2003
- Differential Effects of Inhibitors on the γ-Secretase ComplexJournal of Biological Chemistry, 2003
- γ‐Secretase/presenilin inhibitors for Alzheimer's disease phenocopy Notch mutations inDrosophilaThe FASEB Journal, 2002
- A γ‐secretase inhibitor blocks Notch signaling in vivo and causes a severe neurogenic phenotype in zebrafishEMBO Reports, 2002
- Notch Signaling: Cell Fate Control and Signal Integration in DevelopmentScience, 1999
- Maintenance of pluripotential embryonic stem cells by stem cell selectionReproduction, Fertility and Development, 1998