Rickert Markus, Wang Haili, Wieloch Peter, Lorenz Helga, Steck Eric, Sabo Desiderius, Richter Wiltrud
Department of Orthopaedic Surgery, University of Heidelberg, Heidelberg, Germany.
Connect Tissue Res. 2005;46(4-5):175-83. doi: 10.1080/03008200500237120.
Growth and differentiation factor-5 (GDF-5) is known to induce tendon tissue and stimulate tendon healing. The hypothesis was that adenoviral GDF-5 transfer leads to transitory transgene expression and improves Achilles tendon healing. In vitro experiments were first performed with rat tenocytes. Transgene expression was evaluated by RT-PCR, Western blotting and GDF-5-ELISA. In vivo virus dosage and transgene expression were examined by a marker gene transfer (LacZ and luciferase). In the main experiment in 131 rats, adenovirus particles (3 x 10(10)) were injected into transected Achilles tendons. The time course of GDF-5 mRNA expression was assessed by real-time RT-PCR. Histology and biomechanical testing were used to evaluate tendon healing and tensile strength. In vitro GDF-5 was secreted with a maximum after 2 weeks (330 ng GDF-5/10(6) cells per 24 hr). In vivo GDF-5 transgene expression showed a maximum at 4 weeks. At 8 weeks, GDF-5 specimens were thicker (p<0.05) with a trend to higher strength (p=0,064). Histology showed greater cartilage formation in type II collagen stains than in controls. Injection of adenovirus particles successfully can deliver the GDF-5 gene in healing tendons and leads to thicker tendon regenerates after 8 weeks. This technique might become a new approach for nonsurgical treatment of tendon injuries.
已知生长分化因子-5(GDF-5)可诱导肌腱组织形成并促进肌腱愈合。本研究假设腺病毒介导的GDF-5基因转移可导致短暂的转基因表达并改善跟腱愈合。首先对大鼠肌腱细胞进行了体外实验。通过逆转录聚合酶链反应(RT-PCR)、蛋白质免疫印迹法和GDF-5酶联免疫吸附测定(ELISA)评估转基因表达。通过标记基因转移(LacZ和荧光素酶)检测体内病毒剂量和转基因表达。在131只大鼠的主要实验中,将腺病毒颗粒(3×10¹⁰)注入切断的跟腱中。通过实时RT-PCR评估GDF-5 mRNA表达的时间进程。采用组织学和生物力学测试评估肌腱愈合情况和拉伸强度。体外实验中,GDF-5在2周后分泌量达到最大(每24小时330 ng GDF-5/10⁶个细胞)。体内实验中,GDF-5转基因表达在4周时达到最大。在8周时,GDF-5处理组的肌腱标本更厚(p<0.05),强度有增加趋势(p=0.064)。组织学显示,与对照组相比,II型胶原染色中软骨形成更多。注射腺病毒颗粒能够成功地将GDF-5基因导入愈合中的肌腱,并在8周后使肌腱再生组织更厚。该技术可能成为肌腱损伤非手术治疗的新方法。