Small molecule-based disruption of the Axin/β-catenin protein complex regulates mesenchymal stem cell differentiation

Cell Res. 2012 Jan;22(1):237-47. doi: 10.1038/cr.2011.127. Epub 2011 Aug 9.

Abstract

The Wnt/β-catenin pathway plays important roles in the differentiation of multiple cell types, including mesenchymal stem cells. Using a cell-based chemical screening assay with a synthetic chemical library of 270 000 compounds, we identified the compound SKL2001 as a novel agonist of the Wnt/β-catenin pathway and uncovered its molecular mechanism of action. SKL2001 upregulated β-catenin responsive transcription by increasing the intracellular β-catenin protein level and inhibited the phosphorylation of β-catenin at residues Ser33/37/Thr41 and Ser45, which would mark it for proteasomal degradation, without affecting CK1 and GSK-3β enzyme activities. Biochemical analysis revealed that SKL2001 disrupted the Axin/β-catenin interaction, which is a critical step for CK1- and GSK-3β-mediated phosphorylation of β-catenin at Ser33/37/Thr41 and Ser45. The treatment of mesenchymal stem cells with SKL2001 promoted osteoblastogenesis and suppressed adipocyte differentiation, both of which were accompanied by the activation of Wnt/β-catenin pathway. Our findings provide a new strategy to regulate mesenchymal stem cell differentiation by modulation of the Wnt/β-catenin pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes / cytology
  • Adipocytes / drug effects
  • Adipocytes / metabolism
  • Axin Signaling Complex / metabolism*
  • Cell Differentiation*
  • Enzyme Activation
  • Enzyme Assays
  • Enzyme Inhibitors / metabolism
  • Glycogen Synthase Kinase 3 / metabolism
  • Glycogen Synthase Kinase 3 beta
  • HEK293 Cells
  • Humans
  • Imidazoles / pharmacology
  • Immunoprecipitation
  • Isoxazoles / pharmacology
  • Mesenchymal Stem Cells / cytology*
  • Mesenchymal Stem Cells / drug effects
  • Mesenchymal Stem Cells / metabolism
  • Osteoblasts / cytology
  • Osteoblasts / drug effects
  • Osteoblasts / metabolism
  • Phosphorylation / drug effects
  • Plasmids / genetics
  • Plasmids / metabolism
  • Protein Interaction Mapping
  • Proteolysis
  • Serine / metabolism
  • Threonine / metabolism
  • Transfection
  • Wnt Signaling Pathway*
  • beta Catenin / agonists
  • beta Catenin / metabolism*

Substances

  • 5-furan-2yl-isoxazole-3-carboxylic acid (3-imidazol-1yl-propyl)-amide
  • Axin Signaling Complex
  • Enzyme Inhibitors
  • Imidazoles
  • Isoxazoles
  • beta Catenin
  • Threonine
  • Serine
  • GSK3B protein, human
  • Glycogen Synthase Kinase 3 beta
  • Glycogen Synthase Kinase 3