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Icariin Promotes the Migration of BMSCs In Vitro and In Vivo via the MAPK Signaling Pathway

机译:Icariin通过MAPK信号通路促进BMSCs的体外和体内迁移

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摘要

Bone marrow-derived mesenchymal stem cells (BMSCs) are widely used in tissue engineering for regenerative medicine due to their multipotent differentiation potential. However, their poor migration ability limits repair effects. Icariin (ICA), a major component of the Chinese medical herb Herba Epimedii, has been reported to accelerate the proliferation, osteogenic, and chondrogenic differentiation of BMSCs. However, it remains unknown whether ICA can enhance BMSC migration, and the possible underlying mechanisms need to be elucidated. In this study, we found that ICA significantly increased the migration capacity of BMSCs, with an optimal concentration of 1 μmol/L. Moreover, we found that ICA stimulated actin stress fiber formation in BMSCs. Our work revealed that activation of the MAPK signaling pathway was required for ICA-induced migration and actin stress fiber formation. In vivo, ICA promoted the recruitment of BMSCs to the cartilage defect region. Taken together, these results show that ICA promotes BMSC migration in vivo and in vitro by inducing actin stress fiber formation via the MAPK signaling pathway. Thus, combined administration of ICA with BMSCs has great potential in cartilage defect therapy.
机译:骨髓来源的间充质干细胞(BMSC)由于其多能分化潜能而被广泛用于组织工程中的再生医学。但是,它们的迁移能力差限制了修复效果。 Icariin(ICA)是中草药Herba Epimedii的主要成分,据报道可促进BMSCs的增殖,成骨和软骨分化。但是,ICA是否能增强BMSC的迁移仍是未知的,需要阐明可能的潜在机制。在这项研究中,我们发现ICA可以显着提高BMSC的迁移能力,最适浓度为1μμmol/ L。此外,我们发现ICA刺激了BMSCs中肌动蛋白应激纤维的形成。我们的工作表明,ICA诱导的迁移和肌动蛋白应激纤维形成需要MAPK信号通路的激活。在体内,ICA促进了BMSCs向软骨缺损区域的募集。综上所述,这些结果表明,ICA通过经由MAPK信号传导途径诱导肌动蛋白应激纤维形成来促进体内和体外的BMSC迁移。因此,ICA与BMSC联合给药在软骨缺损治疗中具有巨大潜力。

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