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Updated: Jul 11, 2026

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Published on: October 27, 2020
Activated beta-catenin induces myogenesis and inhibits adipogenesis in BM-derived mesenchymal stromal cells
1Department of Neurology, First Affiliated Hospital, Sun Yat-sen University, Guangzhou, PR China.
Background:
Mesenchymal stromal cells (MSC) have been thought to be attractive candidates for the treatment of degenerative muscle diseases. However, little is known about the molecular mechanisms governing the myogenic differentiation in MSC. As the Wnt signaling pathway has been associated with myogenesis in embryogenesis and post-natal muscle regeneration, we hypothesized that the Wnt signaling pathway may be involved in governing the myogenic differentiation in MSC.
Methods:
Primary MSC were isolated from Sprague-Dawley rats and expanded in proliferation medium. The rMSC were transfected with a constitutively active hbeta-catenin (S37A) plasmid or control vector by Lipofectamine followed by G418 selection. The transfected rMSC were grown to 80% confluence and then cultured in myogenic or adipogenic differentiation medium. Cells were characterized by light microscopy, immunofluorescence and RT-PCR at different time points after myogenic or adipogenic introduction.
Results:
Ectopic expression of activated beta-catenin located primarily in the nucleus and activated transcription in rMSC. Overexpression of stabilized beta-catenin induced 27.1 +/- 3.91% rMSC forming long multinucleated cells expressing MyoD, myogenin, desmin and myosin heavy chain (MHC) via evoking the expression of skeletal muscle-specific transcription factors. In addition, overexpression of activated beta-catenin inhibited the adipogenic differentiation in rMSC through down-regulated expressions of C/EBPalpha and PPARgamma.
Discussion:
To our knowledge, this is the first evidence that activated beta-catenin can induce myogenic differentiation in rMSC. The ability of stabilized beta-catenin to induce myogenic differentiation in rMSC may allow for its therapeutic application.
Insights
Activated beta-catenin induces myogenic differentiation in rat mesenchymal stromal cells (MSC). This finding suggests potential therapeutic applications for degenerative muscle diseases by promoting muscle cell development.
Area of Science:
- Cell Biology
- Regenerative Medicine
- Molecular Biology
Background:
- Mesenchymal stromal cells (MSC) show promise for treating muscle diseases.
- Molecular mechanisms of MSC myogenic differentiation are not fully understood.
- Wnt signaling pathway is implicated in muscle development and regeneration.
Purpose of the Study:
- To investigate the role of the Wnt signaling pathway, specifically beta-catenin, in MSC myogenic differentiation.
- To determine if activating beta-catenin can induce muscle cell formation from MSC.
Main Methods:
- Primary rat MSC were isolated and transfected with activated beta-catenin.
- Transfected MSC were cultured in myogenic or adipogenic differentiation media.
- Cell differentiation was assessed using microscopy, immunofluorescence, and RT-PCR.
Main Results:
- Overexpression of activated beta-catenin led to MSC forming multinucleated muscle cells.
- Activated beta-catenin induced expression of key myogenic markers (MyoD, myogenin, desmin, MHC).
- Activated beta-catenin inhibited adipogenic differentiation by downregulating C/EBPalpha and PPARgamma.
Conclusions:
- This study provides the first evidence that activated beta-catenin can induce myogenic differentiation in rat MSC.
- The findings highlight the potential therapeutic use of stabilized beta-catenin in regenerative medicine for muscle disorders.
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