Ouyang Miao, Li Guo-nian, Zou Yi-you
Department of Gastroenterology, Xiangya Hospital, Central South University, Changsha 410008, China.
Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2007 Dec;32(6):1047-50.
To construct the plasmid of human vascular endothelial cell growth factor165 and green fluorescence protein report gene eukaryotic expression vector of fusion protein pEGFP /hVEGF165, and to detect its expression in vascular endothelial cells.
We amplified full-length of gene VEGF165 by PCR, cloned in direction in multiple clone sites of pEGFP-N1, constructed recombinant plasmid of pEGFP/hVEGF165. Through enzyme digestion, PCR, and sequencing analysis, we also performed liposome-mediated transfection of vascular endothelial cells of in vitro cultivation, and detected the expression of fusion protein pEGFP/hVEGF165 using fluorescence microscope, RT-PCR, and Western blot.
Both gene VEGF165 and multiple clone site of pEGFP-N1 confirmed by PCR, enzyme digestion, and sequence analysis. EGFP/VEGF protein was expressed in vascular endothelial cells after pEGFP/VEGF165 recombinant plasmid transfected vascular endothelial cells.
Fusion protein eukaryotic plasmid of report gene EGFP and VEGF165 is successfully constructed, and EGFP/VEGF can be expressed in vascular endothelial cells, which lays a foundation for the application of VEGF gene in treating ischemia vascular diseases.
构建人血管内皮细胞生长因子165与绿色荧光蛋白报告基因融合蛋白的真核表达载体pEGFP/hVEGF165,并检测其在血管内皮细胞中的表达。
采用PCR扩增VEGF165基因全长,定向克隆至pEGFP-N1的多克隆位点,构建pEGFP/hVEGF165重组质粒。通过酶切、PCR及测序分析,对体外培养的血管内皮细胞进行脂质体介导的转染,并用荧光显微镜、RT-PCR及Western blot检测融合蛋白pEGFP/hVEGF165的表达。
经PCR、酶切及序列分析证实VEGF165基因和pEGFP-N1的多克隆位点正确。pEGFP/VEGF165重组质粒转染血管内皮细胞后,血管内皮细胞中表达了EGFP/VEGF蛋白。
成功构建了报告基因EGFP与VEGF165的融合蛋白真核质粒,且EGFP/VEGF能在血管内皮细胞中表达,为VEGF基因应用于缺血性血管疾病的治疗奠定了基础。