Crosstalk between HIF-1 and ROCK pathways in neuronal differentiation of mesenchymal stem cells, neurospheres and in PC12 neurite outgrowth

Mol Cell Neurosci. 2007 Jul;35(3):409-23. doi: 10.1016/j.mcn.2007.04.002. Epub 2007 Apr 10.

Abstract

This study demonstrates that the Rho-kinase (ROCK) inhibitor, Y-27632, potentiates not only the effect of cobalt chloride (CoCl(2)) but also that of deferoxamine, another HIF-1 inducer, on mesenchymal stem cell (MSC) neuronal differentiation. HIF-1 is essential for CoCl(2)+/-Y-27632-induced MSC neuronal differentiation, since agents inhibiting HIF-1 abolish the changes of morphology and cell cycle arrest-related gene or protein expressions (p21, cyclin D1) and the increase of neuronal marker expressions (Tuj1, NSE). Y-27632 potentiates the CoCl(2)-induced decrease of cyclin D1 and nestin expressions, the increase of HIF-1 activation and EPO expression, and decreases pVHL expression. Interestingly, CoCl(2) decreases RhoA expression, an effect potentiated by Y-27632, revealing crosstalk between HIF-1 and RhoA/ROCK pathways. Moreover, we demonstrate a synergistic effect of CoCl(2) and Y-27632 on neurosphere differentiation into neurons and PC12 neurite outgrowth underlining that a co-treatment targeting both HIF-1 and ROCK pathways might be relevant to differentiate stem cells into neurons.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amides / pharmacology
  • Animals
  • Antimutagenic Agents / pharmacology
  • Cell Differentiation / drug effects
  • Cell Differentiation / physiology*
  • Cell Proliferation / drug effects
  • Cells, Cultured
  • Cobalt / pharmacology
  • Drug Interactions
  • Enzyme Inhibitors / pharmacology
  • Gene Expression Regulation / drug effects
  • Hypoxia-Inducible Factor 1 / metabolism*
  • Intracellular Signaling Peptides and Proteins / metabolism*
  • Mesenchymal Stem Cells / drug effects
  • Mesenchymal Stem Cells / physiology*
  • Mice
  • Nerve Tissue Proteins / metabolism
  • Neurites / drug effects
  • Neurites / metabolism*
  • Neurons / cytology
  • Neurons / drug effects
  • Neurons / physiology*
  • Protein Serine-Threonine Kinases / metabolism*
  • Pyridines / pharmacology
  • Rats
  • Time Factors
  • rho-Associated Kinases

Substances

  • Amides
  • Antimutagenic Agents
  • Enzyme Inhibitors
  • Hypoxia-Inducible Factor 1
  • Intracellular Signaling Peptides and Proteins
  • Nerve Tissue Proteins
  • Pyridines
  • Y 27632
  • Cobalt
  • Protein Serine-Threonine Kinases
  • rho-Associated Kinases
  • cobaltous chloride