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Embryonic Stem Cells/Induced Pluripotent Stem Cells
Article first published online: 19 DEC 2012
Copyright © 2012 AlphaMed Press
Volume 31, Issue 1, pages 35–47, January 2013
How to Cite
Ozair, M. Z., Noggle, S., Warmflash, A., Krzyspiak, J. E. and Brivanlou, A. H. (2013), SMAD7 Directly Converts Human Embryonic Stem Cells to Telencephalic Fate by a Default Mechanism. STEM CELLS, 31: 35–47. doi: 10.1002/stem.1246
Author contributions: M.Z.O.: conception and experimental design, data collection and assembly, analysis and interpretation of data, and manuscript writing; S.N.: conception, data collection and assembly, analysis of data, and manuscript writing; A.W.: analysis and interpretation of data; J.E.K.: data collection and analysis; A.H.B.: conception and design, financial support, data assembly, analysis and interpretation, manuscript writing, and final approval of manuscript.
Disclosure of potential conflicts of interest is found at the end of this article.
First published online in STEM CELLSEXPRESS October 3, 2012.
- Issue published online: 19 DEC 2012
- Article first published online: 19 DEC 2012
- Accepted manuscript online: 3 OCT 2012 03:13PM EST
- Manuscript Accepted: 1 AUG 2012
- Manuscript Received: 13 MAR 2012
- New York State Stem Cell Initiative (NYSTEM) Shared Facilities
- NIH. Grant Number: 2R01HD032105
- The Rockefeller University. S.N. is currently affiliated with the The New York Stem Cell Foundation, 1995 Broadway, NY
- Human embryonic stem cells;
- Neural induction;
- Neural differentiation;
Human embryonic stem cells (hESCs) provide a valuable window into the dissection of the molecular circuitry underlying the early formation of the human forebrain. However, dissection of signaling events in forebrain development using current protocols is complicated by non-neural contamination and fluctuation of extrinsic influences. Here, we show that SMAD7, a cell-intrinsic inhibitor of transforming growth factor-β (TGFβ) signaling, is sufficient to directly convert pluripotent hESCs to an anterior neural fate. Time course gene expression revealed downregulation of MAPK components, and combining MEK1/2 inhibition with SMAD7-mediated TGFβ inhibition promoted telencephalic conversion. Fibroblast growth factor-MEK and TGFβ-SMAD signaling maintain hESCs by promoting pluripotency genes and repressing neural genes. Our findings suggest that in the absence of these cues, pluripotent cells simply revert to a program of neural conversion. Hence, the “primed” state of hESCs requires inhibition of the “default” state of neural fate acquisition. This has parallels in amphibians, suggesting an evolutionarily conserved mechanism. STEM Cells2013;31:35–47