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机构地区:[1]济宁医学院,山东济宁272067 [2]泰山医学院,山东泰安271016
出 处:《济宁医学院学报》2010年第5期305-308,共4页Journal of Jining Medical University
基 金:国家自然科学基金(30971081;81070961);山东省自然科学基金项目(ZR2009DZ004)
摘 要:目的构建与增强型黄色荧光蛋白(EYFP)融合的人Apelin-R(Human Apelin receptor,hApelin-R)真核表达载体,用于Apelin-R介导的细胞内信号转导机制研究。方法以质粒pcDNA3.1-hApelin-R为模板,PCR方法扩增人Apelin-R。扩增的Apelin-R产物与质粒pEYFP-C1按常规方法酶切、连接、转化,并经酶切和测序进行鉴定。将重组质粒用脂质体法转染HEK293细胞,Western blot鉴定人Apelin-R的表达。用Apelin-13诱导后,共聚焦显微镜观察受体在细胞内的位移。结果扩增出了一条1143 bp的基因片段,序列与GenBank(NM_005161)相同。在69 kDa处有一蛋白条带,与预期大小相同。人Apelin-R表达在细胞膜上。诱导30 min后,发生受体向胞浆的位移。结论成功构建了pEYFP-hApelin-R重组表达载体,建立了该质粒转染HEK293的细胞模型。可用于Apelin-R介导的细胞内信号转导机制研究,其结果有助于寻找其作为药物的靶点。Objective To construct expression vector that enhanced yellow fluorescent protein(EYFP)fused with Apelin receptor(Apelin-R),to investigate intercellular signal transduction mechanism mediated by Apelin-R.Methods The human Apelin-R gene was amplified by PCR using the plasmid pcDNA3.1-hApelin-R as template.The PCR product was digested,ligased with the plasmid pEYFP-C1 and then be transformed into the competent cell Top10.The construct was identified by DNA sequencing.The recombinant plasmid was transiently transfected into human embryonic kidney 293(HEK293)cells,and the expression of pEYFP-hApelin-R was detected by confocal microscopy and Western blot.Results A fragment of 1143bp was amplified by PCR,and the DNA sequence was identical with the gene in GenBank(NM_005161).Western blot showed a 69kDa band.Confocal microscopy showed that Apelin-R was expressed on the plasma membrane.However,after induction for 30 min by its ligand Apelin-13,the receptor was endocytosed into cytoplasm.Conclusion The pEYFP-hApelin-R eukaryotic expression vector was successfully constructed,and the expression vector could be used to investigate intercellular signal transduction mechanism mediated by Apelin-R and for drug discovery.
关 键 词:Apelin-R 增强型黄色荧光蛋白 真核表达载体 HEK293细胞
分 类 号:R394[医药卫生—医学遗传学]
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