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作 者:谭晓秋[1] 陈桂兰[1] 李畅[1] 李妙龄[1] 李涛[1] 杨艳[1] 井上勋[1] 曾晓荣[1]
机构地区:[1]泸州医学院心血管医学研究所,医学电生理实验室,四川泸州646000
出 处:《泸州医学院学报》2013年第3期203-206,共4页Journal of Luzhou Medical College
基 金:国家自然科学基金项目(30870903);四川省科技计划(2011FZ0106)
摘 要:目的:克隆人心房肌小电导钙激活钾通道亚型2(SK2),构建稳定表达SK通道的HEK293细胞系并研究其基本电生理学特性。方法:以人心房肌为标本,通过逆转录,重叠PCR法和定向克隆构建真核表达载体pIRES-hrGFP-SK2,采用脂质体法转染至HEK293细胞并筛选稳定表达的细胞系;使用全细胞和单通道膜片钳技术进行电流记录,研究其基本电生理学特性。结果:全细胞和单通道膜片钳均能在表达的HEK293细胞上记录到SK2通道电流,其电流具有明显的胞内钙离子依赖性。结论:成功构建稳定表达人心房肌SK2通道的HEK293细胞系,为以后研究通道功能活动奠定了基础。Objective: To clone the small conductance calcium activated potassium channels type 2(SK2)of human atrial tissue,construct stable HEK293 cells expressed SK2 and investigate the basic electrophysiological properties.Methods: The expression plasmid of pIRES-hrGFP-SK2 was constructed by reverse transcription,overlapping PCR and site-directed cloning.The plasmid was transfected by Lipofectamine 2000 and stable cell lines expressed SK2 were selected.The basic properties of SK2 were investigated by using patch clamp technique.Results: SK2 currents could be recorded in HEK293 cells expressed SK2 channels in whole-cell and single channel configuration.SK2 currents were calcium dependenent.Conclusion: Stable HEK293 cells expressed SK2 are constructed successfully,which establishes the basis for further research about the regulation of SK2 channels.
分 类 号:R331.38[医药卫生—人体生理学]
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