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腺病毒介导的生长分化因子-5基因向肌腱细胞的转移及对大鼠跟腱愈合的影响

Adenovirus-mediated gene transfer of growth and differentiation factor-5 into tenocytes and the healing rat Achilles tendon.

作者信息

Rickert Markus, Wang Haili, Wieloch Peter, Lorenz Helga, Steck Eric, Sabo Desiderius, Richter Wiltrud

机构信息

Department of Orthopaedic Surgery, University of Heidelberg, Heidelberg, Germany.

出版信息

Connect Tissue Res. 2005;46(4-5):175-83. doi: 10.1080/03008200500237120.

Abstract

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.

摘要

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。

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