摘要
背景:人血管内皮生长因子121和骨形态蛋白2在激素性股骨头坏死骨缺损中均具有成血管成骨作用,目前国内在以人血管内皮生长因子121和骨形态蛋白2基因联合治疗激素性股骨头坏死方面少有报道。目的:构建人血管内皮生长因子121与人骨形态发生蛋白2双基因腺病毒穿梭质粒。方法:将质粒pShuttle-CMV-VEGF121-IRES-hrGFP-1经KpnⅠ/XbaⅠ酶切后,将BMP2片段定向连入pShuttle-CMV-VEGF121-IRES,构建可同时表达2个目的基因重组质粒pShuttle-CMV-VEGF121-IRES-BMP2,注入H5a细胞扩增,铺板,筛选阳性菌落,提取质粒,进行酶切分析及序列测定。将已构建确认正确的腺病毒质粒,经BJ5183-AD-1电转感受态细胞进行电穿孔后,铺板,筛选阳性菌落,提取质粒,进行酶切分析,PCR检测和序列分析。结果与结论:酶切分析及核酸序列测定证实重组质粒构建正确,提示实验成功构建了血管内皮生长121及骨形态蛋白2双基因共表达重组腺病毒载体。
BACKGROUND：Vascular endothelial growth factor 121 （VEGF121） and bone morphogenetic protein-2 （BMP-2） play an important role in the development and formation of bones and vessels.At present,there are few reports about the treatment of pathogenesis of steroid-induced avascular necrosis of the femoral head （SANFH） by VEGF121 combined with BMP-2 gene in China.OBJECTIVE：To construct VEGF121 and BMP-2 genes adenovirus shuttle plasmid pShuttle-CMV-V EGF121-IRES-BMP2.METHODS：After Plasmid pShuttle-CMV-VEGF121-IRES-hrGFP-1 through Kpn I/Xba I,BMP-2 fragments were directionally connected to pShuttle-CMV-VEGF121-IRES.Simultaneous expression of two gene plasmid pShuttle-CMV-VEGF121-IRES was constructed,and injected with H5a cells expansion,planking,screening positive colonies,extracting plasmid,and then was undergo restriction analysis and sequencing.The correct adenovirus plasmid which has been constructed and confirmed after through BJ5183-AD-1 electroporation competent cells was undergo the electroporation,planking,screening positive colonies,extracting plasmid,and was undergo restriction analysis,PCR detection,and sequence analysis.RESULTS AND CONCLUSION：Construction of the adenovirus shuttle plasmid was correct according to restriction analysis and nucleotide sequence detection confirmed.It is indicated that VEGF121 and BMP-2 genes co-expressing recombinant adenovirus vector can be constructed successfully in the experiment.
出处
《中国组织工程研究与临床康复》
CAS
CSCD
北大核心
2011年第20期3741-3744,共4页
Journal of Clinical Rehabilitative Tissue Engineering Research
