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血管内皮生长因子基因转染促进兔股骨头缺血性坏死修复

Vascular endothelial growth factor gene transfection to enhance the repair of avascular necrosis of the femoral head of rabbit.

作者信息

Yang Cao, Yang Shuhua, Du Jingyuan, Li Jin, Xu Weihua, Xiong Yufang

机构信息

Department of Orthopedics, Union Hospital, Tongji Medical College, Huazhong University of Science & Technology, Wuhan 430022, China.

出版信息

Chin Med J (Engl). 2003 Oct;116(10):1544-8.

Abstract

OBJECTIVE

To explore a new method for the therapy of avascular necrosis of the femoral head.

METHODS

The recombinant plasmid pCD-hVEGF165 was mixed with collagen and was implanted in the necrotic femoral head. The expression of vascular endothelial growth factor (VEGF) was examined by RNA dot hybridization and immunohistochemical techniques. Repair of the femoral head was observed by histological and histomorphometric analysis.

RESULTS

The expression of VEGF was detected in the femoral head transfected with the VEGF gene. The femoral head transfected with the VEGF gene showed a significant increase in angiogenesis 2 and 4 weeks after gene transfection and a significant increase in bone formation 6 and 8 weeks after gene transfection on histomorphometric analysis (P < 0.01).

CONCLUSIONS

Transfection of the VEGF gene enhances bone tissue angiogenesis. Repair of osteonecrosis could be accelerated accordingly, thus providing a potential method for therapy of osteonecrosis.

摘要

目的

探索一种治疗股骨头缺血性坏死的新方法。

方法

将重组质粒pCD-hVEGF165与胶原蛋白混合后植入坏死的股骨头。采用RNA斑点杂交和免疫组化技术检测血管内皮生长因子(VEGF)的表达。通过组织学和组织形态计量学分析观察股骨头的修复情况。

结果

在转染VEGF基因的股骨头中检测到VEGF的表达。组织形态计量学分析显示,转染VEGF基因的股骨头在基因转染后2周和4周血管生成显著增加,在基因转染后6周和8周骨形成显著增加(P < 0.01)。

结论

VEGF基因转染可增强骨组织血管生成。相应地可加速骨坏死的修复,从而为骨坏死的治疗提供一种潜在方法。

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