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作 者:胡莎莎 应永军[2] 卢瑛[1] HU Shasha;YING Yongjun;LU Ying(Department of Functional Inspection,Tongde Hospital of Zhejiang Province,Hangzhou 310012,China;不详)
机构地区:[1]浙江省立同德医院功能检查科,杭州310012 [2]浙江省立同德医院心内科,杭州310012
出 处:《心电与循环》2022年第4期326-330,I0002,共6页Journal of Electrocardiology and Circulation
基 金:浙江省医学会临床科研资金项目(2015ZYC-A10)。
摘 要:目的探讨CCAAT/增强子结合蛋白β(C/EBPβ)对心房肌细胞KCNQ1基因表达的调控作用。方法利用生物信息分析和转录因子筛选板筛选出C/EBPβ作为KCNQ1的转录因子。用5-Hz电刺激快速起搏心房肌细胞。用染色质免疫沉淀法检测C/EBPβ、KCNQ1 m RNA和蛋白的表达水平。将心房肌细胞转染慢病毒并分为对照组、C/EBPβ抑制组和过表达组,采用荧光定量PCR和蛋白质印迹技术检测KCNQ1的表达水平;采用膜片钳测定Iks膜电位和电流峰值。结果C/EBPβ参与了KCNQ1的转录,心房肌细胞中C/EBPβ、KCNQ1 m RNA和蛋白的表达水平快速起搏下显著高于非快速起搏下(均P<0.05)。与对照组比较,C/EBPβ抑制组KCNQ1 m RNA表达和Iks电流显著降低而C/EBPβ过表达组显著升高(均P<0.05)。结论C/EBPβ可能对心房肌细胞KCNQ1基因的表达有调控作用。Objective To explore the regulatory effect of CCAAT/enhancer binding protein beta(C/EBPβ)on KCNQ1 gene expression in atrial myocytes.Methods C/EBPβwas selected as a transcription factor for KCNQ1 by using bioinformatics analysis and TF Activation Profiling Plate Array.Rapid pacing of atrial myocytes was achieved by5-Hz electrical stimulation.Chromatin immunoprecipitation was used to detect the expression levels of C/EBPβ,KCNQ1m RNA and protein.Atrial myocytes were transfected with lentivirus and divided into control group,C/EBPβinhibition group and overexpression group.The expression level of KCNQ1 was detected by fluorescence quantitative PCR and Western blotting.Membrane potential and peak current of Ikswere measured by patch clamp technique.Results C/EBPβwas involved in the transcription of KCNQ1.The expression levels of C/EBPβ,KCNQ1 m RNA and protein were significantly higher in atrial myocytes in the presence of rapid pacing than in the absence of rapid pacing(all P<0.05).Compared with the control group,KCNQ1 m RNA and Ikscurrent decreased significantly in C/EBPβinhibition group and increased significantly in C/EBPβoverexpression group(all P<0.05).Conclusion C/EBPβmay have regulatory effect on KCNQ1 gene expression of atrial myocytes.
关 键 词:心房肌细胞 KCNQ1 CCAAT/增强子结合蛋白β 转录调控
分 类 号:R541.75[医药卫生—心血管疾病]
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