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利用产生转化生长因子β1的成纤维细胞通过细胞介导的基因疗法再生透明软骨。

Regeneration of hyaline cartilage by cell-mediated gene therapy using transforming growth factor beta 1-producing fibroblasts.

作者信息

Lee K H, Song S U, Hwang T S, Yi Y, Oh I S, Lee J Y, Choi K B, Choi M S, Kim S J

机构信息

Department of Orthopedic Surgery, College of Medicine, Inha University, Inchon, South Korea 400-711.

出版信息

Hum Gene Ther. 2001 Sep 20;12(14):1805-13. doi: 10.1089/104303401750476294.

Abstract

Transforming growth factor beta (TGF-beta) has been considered as a candidate for gene therapy of orthopedic diseases. The possible application of cell-mediated TGF-beta gene therapy as a new treatment regimen for degenerative arthritis was investigated. In this study, fibroblasts expressing active TGF-beta 1 were injected into the knee joints of rabbits with artificially made cartilage defects to evaluate the feasibility of this therapy for orthopedic diseases. Two to 3 weeks after the injection there was evidence of cartilage regeneration, and at 4 to 6 weeks the cartilage defect was completely filled with newly grown hyaline cartilage. Histological analyses of the regenerated cartilage suggested that it was well integrated with the adjacent normal cartilage at the sides of the defect and that the newly formed tissue was indeed hyaline cartilage. Our findings suggest that cell-mediated TGF-beta 1 gene therapy may be a novel treatment for orthopedic diseases in which hyaline cartilage damage has occurred.

摘要

转化生长因子β(TGF-β)被认为是骨科疾病基因治疗的一个候选因子。研究了细胞介导的TGF-β基因治疗作为退行性关节炎新治疗方案的可能应用。在本研究中,将表达活性TGF-β1的成纤维细胞注射到人工制造软骨缺损的兔膝关节中,以评估这种治疗骨科疾病的可行性。注射后2至3周有软骨再生的迹象,4至6周时软骨缺损被新生长的透明软骨完全填充。对再生软骨的组织学分析表明,它在缺损边缘与相邻的正常软骨良好整合,并且新形成的组织确实是透明软骨。我们的研究结果表明,细胞介导的TGF-β1基因治疗可能是一种针对已发生透明软骨损伤的骨科疾病的新治疗方法。

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