Understanding the mechanism of the differentiation of induced pluripotent stem cells (iPSCs) into mesenchymal stem cells (MSCs) and promoting the production efficiency of iPSC-derived MSCs (iPSC-MSCs) are critical to periodontal tissue engineering. However, the gene networks that control this differentiation process from iPSCs into MSCs are poorly understood. We demonstrated that MFN2 knockdown showed a positive effect on the triploblastic and MSC differentiation from iPSCs. Activation of the PI3K/Akt signaling pathway by MFN2 knockdown activated the Wnt/β-catenin signaling pathway by inhibiting GSK-3β and reducing β-catenin degradation. Inhibitor of the PI3K/Akt signaling pathway normalized the enhanced efficiency of differentiation into MSCs of MFN2-KD iPSCs and Wnt activator-treated control iPSCs. MFN2-OE iPSCs displayed an opposite phenotype. In conclusion, downregulating MFN2 promotes the differentiation of iPSCs into MSCs by activating the PI3K/Akt/GSK-3β/Wnt signaling pathway. Our results reveal a crucial function and mechanism for MFN2 in regulating MSC differentiation from iPSCs, which will provide new ideas for periodontal tissue engineering and periodontal regenerative treatment by using iPSC-MSCs.
Keywords: MFN2; PI3K/Akt signaling pathway; Wnt/β-catenin signaling pathway; differentiation; induced pluripotent stem cells; mesenchymal stem cells.