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Gene- and stem cell-based therapeutics for cartilage regeneration and repair

机译:基因和干细胞的疗法用于软骨再生和修复

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Cell-based regeneration of damaged or diseased articular cartilage still faces significant clinical challenge due to inadequate environmental regulation of stem cell proliferation and chondrogenic differentiation. The role of insulin-like growth factor in critical steps of human bone marrow-derived mesenchymal stem cell chondrogenesis has potential in optimizing the therapeutic use of mesenchymal stem cells in cartilage disorders. In addition to the previously described benefits of recombinant adeno-associated viral vector for in vivo gene therapy, demonstrated by Frisch and colleagues, such vector is also a safe and efficient delivery system for the genetic modification of human bone marrow-derived mesenchymal stem cells via ex vivo insulin-like growth factor 1 gene transfer, so that implanted mesenchymal stem cells continuously release a therapeutic level of insulin-like growth factor 1 to achieve sustained mesenchymal stem cell chondrogenesis for cartilage regeneration.
机译:由于干细胞增殖和软骨内分化的环境调节不足,损伤或患病关节软骨的细胞的再生仍然面临着显着的临床攻击。胰岛素样生长因子在人骨髓间充质干细胞软骨发生中临界步骤中的作用具有优化在软骨障碍中的化间充质干细胞的治疗用途。除了通过Frisch和同事证明的体内基因治疗的重组腺相关病毒载体的先前描述的重组腺相关病毒载体外,这种载体也是一种安全有效的递送系统,用于通过离体胰岛素样生长因子1基因转移,因此植入的间充质干细胞连续释放胰岛素样生长因子1的治疗水平,以实现软骨再生的持续间充质干细胞软骨发生。

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