| Literature DB >> 21826110 |
Jungsug Gwak1, Sun Gwan Hwang, Hyung-Soon Park, Sang Rak Choi, Sun-Hee Park, Hyunjoon Kim, Nam-Chul Ha, Sung Jin Bae, Jin-Kwan Han, Dong-Eun Kim, Jeong Woo Cho, Sangtaek Oh.
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.Entities:
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Year: 2011 PMID: 21826110 PMCID: PMC3351914 DOI: 10.1038/cr.2011.127
Source DB: PubMed Journal: Cell Res ISSN: 1001-0602 Impact factor: 25.617