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作 者:陈成[1] 王桂华[1] 李兆明[1] 李小兰[1] 陶德定[1] 龚建平[1] 胡俊波[1]
机构地区:[1]华中科技大学同济医学院附属同济医院胃肠外科,武汉430030
出 处:《华中科技大学学报(医学版)》2012年第5期509-512,共4页Acta Medicinae Universitatis Scientiae et Technologiae Huazhong
基 金:国家"973"计划资助项目(No.2009CB521802);国家自然科学基金资助项目(No.30872472;30973496;30800569)
摘 要:目的研究癌基因c-myc对人结肠癌细胞LoVo中缺氧诱导因子-1α(HIF-1α)的影响及其对血管生成的作用。方法构建高表达c-myc的质粒pcDNA3.1-c-myc;将构建好的pcDNA3.1-c-myc质粒转染入LoVo细胞系中,通过Western blot检测c-myc在LoVo细胞中的表达情况。应用real-time PCR和Western blot检测常氧和乏氧状态下LoVo细胞系中HIF-1α、血管内皮生长因子(VEGF)的mRNA水平及HIF-1α的蛋白水平。应用条件培养液培养人脐静脉内皮细胞(HUVECs),观察其形成血管的能力。结果成功构建pcDNA3.1-c-myc质粒;常氧、乏氧状态下转染pcD-NA3.1-c-myc质粒后,LoVo细胞系中HIF-1α的mRNA水平无变化,VEGF的mRNA水平明显升高,HIF-1α蛋白水平明显增高。高表达c-myc的LoVo细胞上清液培养HUVECs细胞后能增强其成管能力。结论在LoVo细胞系中高表达c-myc,可以促进细胞HIF-1α和其下游的VEGF表达,从而促进血管生成。Objective To investigate the influence of c-myc on HIF-1α in LoVo cell line and the effect on angiogenesis.Methods Plasmid pcDNA3.1-c-myc was constructed and transfected into LoVo cells.The transfection efficiency was tested by using Western blot.The mRNA expression level of HIF-1α and VEGF,and the protein expression level of HIF-1α were detected by using real-time PCR and Western blot under normoxia and hypoxia.Conditioned medium was applied to culture HUVECs and the ability of tube information was examined.Results The plasmid pcDNA3.1-c-myc was successfully constructed.Real-time PCR showed that the mRNA level of HIF-1α had no significant changes under normoxia and hypoxia.The protein expression level of HIF-1α was significantly increased,and the mRNA expression level of VEGF was obviously increased.The ability of tube formation by HUVECs was augmented through the overexpression of c-myc.Conclusion Overexpression of c-myc in LoVo cells can significantly increase the expression of HIF-1α and its downstream VEGF,and then promote angiogenesis.
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