SMAD7 directly converts human embryonic stem cells to telencephalic fate by a default mechanism

Stem Cells. 2013 Jan;31(1):35-47. doi: 10.1002/stem.1246.


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.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Brain / embryology
  • Brain / metabolism
  • Cell Line
  • Embryonic Stem Cells / cytology
  • Embryonic Stem Cells / physiology*
  • Fibroblast Growth Factors / metabolism
  • Humans
  • MAP Kinase Signaling System
  • Mitogen-Activated Protein Kinases / metabolism
  • Neurogenesis
  • Pluripotent Stem Cells / metabolism
  • Smad7 Protein / metabolism*
  • Telencephalon / cytology*
  • Telencephalon / embryology*
  • Telencephalon / metabolism
  • Transforming Growth Factor beta / metabolism


  • SMAD7 protein, human
  • Smad7 Protein
  • Transforming Growth Factor beta
  • Fibroblast Growth Factors
  • Mitogen-Activated Protein Kinases