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Human mesenchymal stem cells overexpressing therapeutic genes: From basic science to clinical applications for articular cartilage repair

机译:人间充质干细胞过表达治疗基因:从基础科学到关节软骨修复的临床应用

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摘要

Adult articular cartilage has a limited capacity for self repair. Reproduction of a native structure and functional integrity in damaged cartilage remains a major problem in orthopaedic surgery. Strategies based on the implantation of genetically modified cells to sites of injury may provide workable options to treat articular cartilage lesions like those resulting from acute trauma or associated with the progression of osteoarthritis. Mesenchymal stem cells have remarkable properties that make them an attractive source of cells to treat cartilage disorders due to their self-renewal capability, stemness maintenance, and chondrogenic differentiation potential. For these reasons, such progenitor cells might be further modified by gene transfer protocols to reinforce their potency and consequently, to enhance the healing processes in damaged tissue following transplantation in sites of cartilage injury. Here, we propose an overview of the current approaches employed for cell-and gene-based treatment of articular cartilage disorders using mesenchymal stem cells.
机译:成人关节软骨的自我修复能力有限。受损软骨中天然结构和功能完整性的再生仍然是整形外科的主要问题。基于转基因细胞植入损伤部位的策略可能为治疗关节软骨损伤提供可行的选择,例如由急性创伤或与骨关节炎进展相关的损伤。间充质干细胞具有非凡的特性,使其具有自我更新的能力,干性维持能力和软骨分化潜能,因此成为治疗软骨疾病的诱人细胞来源。由于这些原因,可以通过基因转移方案进一步修饰此类祖细胞,以增强其效力,从而增强在软骨损伤部位移植后受损组织中的愈合过程。在这里,我们提出了使用间充质干细胞对基于细胞和基因的关节软骨疾病进行治疗的当前方法的概述。

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