Neurotrophins mediate human embryonic stem cell survival

Nat Biotechnol. 2006 Mar;24(3):344-50. doi: 10.1038/nbt1189. Epub 2006 Jan 29.


Growth of human embryonic stem (hES) cells as a pluripotent population requires a balance between survival, proliferation and self-renewal signals. Here we demonstrate that hES cells express receptors of the tropomyosin-related kinase (TRK) family, which mediate antiapoptotic signals. We show that three TRK ligands, brain-derived neurotrophic factor, neurotrophin 3 and neurotrophin 4, are survival factors for hES cells. Addition of neurotrophins to hES cell cultures effects a 36-fold improvement in their clonal survival. hES cell cultures maintained in medium containing neurotrophins remain diploid and retain full developmental potency. In the presence of neurotrophins, TRK receptors in hES cells are phosphorylated; TRK receptor inhibition leads to hES cell apoptosis. The survival activity of neurotrophins in hES cells is mediated by the phosphatidylinositol-3-kinase pathway but not the mitogen-activated protein kinase pathway. Neurotrophins improve hES cell survival and may facilitate their manipulation and the development of high-throughput screens to identify factors responsible for hES cell differentiation.

Publication types

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

MeSH terms

  • Brain-Derived Neurotrophic Factor / metabolism*
  • Brain-Derived Neurotrophic Factor / pharmacology
  • Cell Survival / drug effects
  • Cells, Cultured
  • Clone Cells / drug effects
  • Clone Cells / metabolism
  • Dose-Response Relationship, Drug
  • Humans
  • Nerve Growth Factors / metabolism*
  • Nerve Growth Factors / pharmacology
  • Neurotrophin 3 / metabolism*
  • Neurotrophin 3 / pharmacology
  • Phosphatidylinositol 3-Kinases / metabolism
  • Phosphorylation / drug effects
  • Receptor, trkB / metabolism
  • Receptor, trkC / metabolism
  • Stem Cells / cytology*


  • Brain-Derived Neurotrophic Factor
  • Nerve Growth Factors
  • Neurotrophin 3
  • Phosphatidylinositol 3-Kinases
  • Receptor, trkB
  • Receptor, trkC
  • neurotrophin 4