首页> 美国卫生研究院文献>International Journal of Clinical and Experimental Medicine >Vascular endothelial growth factor/bone morphogenetic protein-2 bone marrow combined modification of the mesenchymal stem cells to repair the avascular necrosis of the femoral head
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Vascular endothelial growth factor/bone morphogenetic protein-2 bone marrow combined modification of the mesenchymal stem cells to repair the avascular necrosis of the femoral head

机译:血管内皮生长因子/骨形态发生蛋白2骨髓联合修饰间充质干细胞修复股骨头缺血性坏死

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摘要

Vascular endothelial cell growth factor (VEGF) combined with bone morphogenetic protein (BMP) was used to repair avascular necrosis of the femoral head, which can maintain the osteogenic phenotype of seed cells, and effectively secrete VEGF and BMP-2, and effectively promote blood vessel regeneration and contribute to formation and revascularization of tissue engineered bone tissues. To observe the therapeutic effect on the treatment of avascular necrosis of the femoral head by using bone marrow mesenchymal stem cells (BMSCs) modified by VEGF-165 and BMP-2 in vitro. The models were avascular necrosis of femoral head of rabbits on right leg. There groups were single core decompression group, core decompression + BMSCs group, core decompression + VEGF-165/BMP-2 transfect BMSCs group. Necrotic bone was cleared out under arthroscope. Arthroscopic observation demonstrated that necrotic bone was cleared out in each group, and fresh blood flowed out. Histomorphology determination showed that blood vessel number and new bone area in the repair region were significantly greater at various time points following transplantation in the core decompression + VEGF-165/BMP-2 transfect BMSCs group compared with single core decompression group and core decompression + BMSCs group (P < 0.05). These suggested that VEGF-165/BMP-2 gene transfection strengthened osteogenic effects of BMSCs, elevated number and quality of new bones and accelerated the repair of osteonecrosis of the femoral head.
机译:血管内皮细胞生长因子(VEGF)结合骨形态发生蛋白(BMP)修复股骨头缺血性坏死,可维持种子细胞的成骨表型,并有效分泌VEGF和BMP-2,并有效促进血液血管再生,有助于组织工程骨组织的形成和血运重建。观察使用VEGF-165和BMP-2修饰的骨髓间充质干细胞(BMSCs)体外治疗股骨头缺血性坏死的疗效。该模型是右腿兔股骨头的无血管坏死。各组分为单核减压组,核减压+ BMSCs组,核减压+ VEGF-165 / BMP-2转染BMSCs组。在关节镜下清除坏死骨。关节镜观察显示,每组清除了坏死骨,新鲜血液流出。组织形态学测定表明,与单核心减压组和核心减压+ BMSCs相比,核心减压+ VEGF-165 / BMP-2转染BMSCs组移植后各个时间点修复区的血管数目和新骨面积明显增加。组(P <0.05)。这些提示VEGF-165 / BMP-2基因转染增强了BMSCs的成骨作用,提高了新骨的数量和质量,并加速了股骨头骨坏死的修复。

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