设为首页| 加入收藏
网站首页 本刊简介 编委会 投稿指南 过刊浏览 联系我们 下载专区
最新消息:
位置:首页 >> 期刊文章
Hint2基因过表达质粒的构建及其对肝癌细胞BEL-7402迁移的影响
作者:李奇萌  林国南 
单位:首都医科大学 北京 100069 
关键词:Hint2 pcDNA3.1(+) BEL-7402细胞 
分类号:
出版年,卷(期):页码:2018,10(3):1-6
摘要:
摘要:目的 探讨Hint2基因过表达质粒的构建及其对肝癌细胞BEL-7402迁移的影响。方法 根据Hint2基 因设计引物,扩增Hint2基因全长并以pcDNA3.1(+)为载体构建Hint2过表达质粒。转染BEL-7402细 胞提取mRNA和总蛋白,分别使用Real-time PCR和Western blot检测转染细胞Hint2 mRNA和蛋白质表达 的变化,应用免疫荧光染色法对细胞中Hint2蛋白与细胞线粒体进行共定位。使用划痕愈合实验检测 Hint2过表达后对肝癌细胞BEL-7402迁移能力的影响。结果 转染Hint2过表达质粒细胞的Hint2 mRNA和 蛋白表达显著上调,免疫荧光染色表明过表达的Hint2蛋白定位于线粒体。划痕愈合实验表明Hint2过表 达质粒使肝癌细胞BEL-7402迁移速率显著降低。结论 Hint2过表达质粒能够上调BEL-7402细胞中Hint2 mRNA和蛋白质的表达水平,表达的蛋白定位于细胞线粒体并抑制肝癌细胞的迁移。
Abstract: Objective To investigate the construction of Hint2 overexpression plasmid and its effect on invasion capability of liver cancer cell BEL-7402. Methods According to the sequence of Hint2 gene, primers were designed to amplify Hint2 gene fragment for Hint2 gene overexpression plasmid construction. mRNA and total protein were extracted from Hint2 overexpressed BEL-7402 cells, real-time PCR and Western blot were applied to determine the expression levels of Hint2, and then the location of exogenous Hint2 in mitochondria was confirmed through immunorescence staining. Subsequently, wound healing experiment was taken to detect the changes of invasion and migration capability of BEL-7402 cells after Hint2 overexpression. Results The mRNA and protein expression levels of Hint2 up-regulated significantly in BEL-7402 cells after transfection with Hint2 overexpression plasmid. According to the result of immunofluorescence staining, the exogenous Hint2 protein was co-located with the mitochondria. Wound healing experiment showed the up-regulation of Hint2 restrained the migration ability in BEL-7402 cells. Conclusion After transfection with Hint2 overexpression plasmid, the expression level of Hint2, which was bound with mitochondria, was increased and the migration ability of BEL-7402 cells was restrained.
基金项目:
作者简介:
参考文献:
服务与反馈:
文章下载】【加入收藏
 

地址:北京市朝阳区京顺东街8号
邮政编码:100015  电话:010-84322058  传真:010-84322059 Email:editordt@163.com