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Osteogenesis induced in goat bone marrow progenitorcells by recombinant adenovirus coexpressing bone morphogenetic protein 2 andbasic fibroblast growth factor

机译:山羊骨髓祖细胞诱导成骨重组腺病毒共表达骨形态发生蛋白2和碱性成纤维细胞生长因子

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摘要

Bone morphogenetic protein 2 (BMP2) and basic fibroblast growth factor (bFGF) have been shown to exhibit a synergistic effect to promote bone repair and healing. In this study, we constructed a novel adenovirus with high coexpression of BMP2 and bFGF and evaluated its effect on osteogenic differentiation of goat bone marrow progenitor cells (BMPCs). Recombinant adenovirus Ad-BMP2-bFGF was constructed by using the T2A sequence. BMPCs were isolated from goats by density gradient centrifugation and adherent cell culture, and were then infected with Ad-BMP2-bFGF or Ad-BMP2. Expression of BMP2 and bFGF was detected by ELISA, and alkaline phosphatase (ALP) activity was detected by an ALP assay kit. In addition, von Kossa staining and immunocytochemical staining of collagen II were performed on BMPCs 21 days after infection. There was a high coexpression of BMP2 and bFGF in BMPCs infected with Ad-BMP2-bFGF. Twenty-one days after infection, ALP activity was significantly higher in BMPCs infected with Ad-BMP2-bFGF than in those infected with Ad-BMP2. Larger and more mineralized calcium nodules, as well as stronger collagen II staining, were observed in BMPCs infected with Ad-BMP2-bFGF than in those infected with Ad-BMP2. In summary, we developed a novel adenovirus vector Ad-BMP2-bFGF for simultaneoushigh coexpression of BMP2 and bFGF, which could induce BMPCs to differentiateefficiently into osteoblasts.
机译:骨形态发生蛋白2(BMP2)和碱性成纤维细胞生长因子(bFGF)已显示出协同作用,可促进骨修复和愈合。在这项研究中,我们构建了一种新型的BMP2和bFGF高表达的腺病毒,并评估了其对山羊骨髓祖细胞(BMPCs)成骨分化的影响。通过使用T2A序列构建重组腺病毒Ad-BMP2-bFGF。通过密度梯度离心和贴壁细胞培养从山羊中分离出BMPC,然后用Ad-BMP2-bFGF或Ad-BMP2感染。通过ELISA检测BMP2和bFGF的表达,并且通过ALP测定试剂盒检测碱性磷酸酶(ALP)活性。另外,感染后21天,在BMPC上进行了胶原蛋白II的von Kossa染色和免疫细胞化学染色。在感染了Ad-BMP2-bFGF的BMPC中,BMP2和bFGF的高表达。感染后21天,感染Ad-BMP2-bFGF的BMPC中的ALP活性明显高于感染Ad-BMP2的BMPC。在感染Ad-BMP2-bFGF的BMPC中,观察到比感染Ad-BMP2的BMPC更大,更矿化的钙结节,以及更强的II型胶原蛋白染色。总之,我们开发了一种新型的腺病毒载体Ad-BMP2-bFGFBMP2和bFGF的高共表达,可能诱导BMPC分化有效地变成成骨细胞。

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