期刊文献+

COS-7细胞株中KCNE2与KChIP2c共表达对Kv4.2电流复活的影响 被引量:1

The effect of co-expression of KCNE2 and KChIP2c on Kv42 current recovery from inactivation of COS-7 cells
下载PDF
导出
摘要 目的探讨当钾通道相互作用蛋白(KChIP2)和KCNE2共表达时对电压依赖性钾通道Kv4.2电流复活的影响。方法采用COS-7株细胞表达系统模拟生理条件,将Kv4.2、KChIP2c和KCNE2 cDNA以3∶1∶1的分子比同时转染至COS-7株细胞,用膜片钳的方法记录全细胞电流,用免疫组化聚焦实验和免疫荧光成像证实细胞表达cDNAs编码的蛋白质。结果 KChIP2c加速了Kv4.2的复活,KCNE2与KChIP2c共表达进一步加速了电流的复活,导致了在Kv4.2电流恢复中的"超射"峰电流,一种人类瞬间外向电流(Ito)特有的现象。结论 Kv4.2与KChIP2c和KCNE2的共表达可产生与人类天然Ito相似的电流,提示KChIP2c和KCNE2同时参与构成心肌细胞Ito的电生理特性。 Objective To study the effect of co-expression of KCNE2 and KChIP2c on voltage-dependent K+ channel Kv4.2 current recovery from inactivation of COS-7 cells.Methods The expression of COS-7 cells was used to simulate physiological conditions.Kv4.2,KChIP2c and KCNE2 cDNA were simultaneously transfected into COS-7 cells at a molar ratio of 3:1:1.Whole-cell current was recorded by patch-clamp method.Proteins encoded by cDNAs were detected by immunocytochemical confocal experiment,and immunofluorescence was imaged with fluorescent microscopy.Results KChIP2c accelerated Kv4.2 recovery from inactivation.Co-expression of KCNE2 and KChIP2c further accelerated the recovery and caused an "over-shoot" of peak current amplitude during Kv4.2 current recovery,a phenomenon which has been uniquely described for human transient outward current(Ito).Conclusion Co-expression of Kv4.2 with KChIP2c and KCNE2 yields a current profile similar to human native Ito.Both KChIP2c and KCNE2 simultaneously participate in recapitulation of electrophysiological properties of Ito in cardiomyocytes.
出处 《临床和实验医学杂志》 2012年第13期993-995,998,共4页 Journal of Clinical and Experimental Medicine
基金 深圳市南山区卫生科技计划项目基金资助(项目编号:2009017)
关键词 瞬间外向电流 钾通道相互作用蛋白 KCNE2 电生理 Transient outward current KChIP2 KCEN2 Electrophysiology
  • 相关文献

参考文献14

  • 1Kurokawa J, Bankstan JR, Kaihara A, et al. KCNE variants reveal a critical role of the beta subunit carboxyl terminus in PKA - dependent regulation of the IKs potassium channel[J]. Channels (Austin), 2009, 3(1) :16-24.
  • 2McCrossan ZA, Roepke TK, Lewis A, et al. Regulation of the Kv2.1 potassium channel by MinK and MiRP1 [ J ]. J Membr Biol, 2009,228 (1) :1 -14.
  • 3Kundu P, Ciobotaru A, Foroughi S, et al. Hormonal regulation of car- diac KCNE2 gene expression [ J ]. Mol Cell Endocfinol, 2008,292 (1 - 2) :50 -62.
  • 4Deschnes I, DiSilvestre D, Juang GJ, et al. Regulation of Kv4.3 cur- rent by KChIP2 splice variants: a component of native cardiac I (to) [J] ? Circulation, 2002,106(4) :423 -429.
  • 5Jiang M, Zhang M, Tang DG, et al. KCNE2 protein is expressed in ventricles of different species, and changes in its expression contribute to electrical remodeling in diseased hearts [ J ]. Circulation, 2004, 109 (14) : 1783 - 1788.
  • 6Zhang M, Jiang M, Tseng GN. minK - related peptide 1 associates with Kv4.2 and modulates its gating function: potential role as beta subunit of cardiac transient outward channel [ J ] ? Circ Res, 2001,88 ( 10 ) : 1012 - 1019.
  • 7Patel SP, Campbell DL, Morales MJ, et al. Heterogeneous expression of KChIP2 isoforms in the ferret heart[ J]. J Physiol, 2002,539 (Pt 3 ) : 649 - 656.
  • 8Hosati B, Grau F, Hodnguez S, et al. Concordant expression ofKChIP2 mRNA, protein and transient outward current throughout the ca- nine ventricle[ J]. J Physiol, 2003,548 ( Pt 3 ) :815 - 822.
  • 9Rosati B, Pan Z, Lypen S, et al. Regulation of KChlP'2 potassium channel beta subunit gene expression underlies the gTadient of transient outward current in canine and human ventricle[ Jl. J Physiol, 2001, 533(Pt 1) :119 -125.
  • 10Ravn LS, Aizawa Y, Pollevick GD, et al. Gain of function in IKs sec- ondary to a mutation in KCNE5 associated with atrial fibrillation [ J 1. Heart Rhythm, 2008,5(3) :427 -435.

二级参考文献11

  • 1Abbott GW,Sesti F,Splawski I,et al.MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia[J].Cell,1999,97(2):175-87.
  • 2Sanguinetti MC,Curran ME,Zou A,et al.Coassembly of KvLQT1 and mink (IsK) proteins to form cardiac IKs potassium channel[J].Nature,1996,384:80-3.
  • 3Tinel N,Diochot S,Borsotto M,et al.KCNE2 confers background current characteristics to the cardiac KCNQ1 potassium channel[J].EMBO,2000,19(23):6326-30.
  • 4Zhang M,Jiang M,Tseng GN.Mink-related peptide 1 associates with Kv4.2 and modulates its gating function.A potential role as β subunit of cardiac transient outward channel[J].Circ Res,2001,88(10):1012-9.
  • 5Dixon JE,Shi W,Wang H-S,et al.Role of the Kv4.3 K+ channel in ventricular muscle.A molecular correlate for the transient outward current[J].Circ Res,1996,79(4):659-68.
  • 6Qin D,Huang B,Deng L,et al.Downregulation of K(+) channel genes expression in type Ⅰ diabetic cardiomyopathy[J].Biochem Biophys Res Commun,2001,11,283(3):549-53.
  • 7Keating MT,Sanguinetti MC.Molecular and cellular mechanisms of cardiac arrhythmias[J].Cell,2001,104(4):569-80.
  • 8Gavin Y,Oudit,Zamaneh Kassiri,et al.The molecular physiology of the cardiac transient outward potassium current (Ito) in normal and diseased myocardium[J].J Mol Cell Cardiol,2001,33(5):851-72.
  • 9Amberg GC,Bonev AD,Rossow CF,et al.Modulation of the molecular composition of large conductance,Ca^2+ activated K^+ channels in vascular smooth muscle during hypertension[J].J Clin Invest,2003,112(5):717-24.
  • 10Jiang M,Zhang M,Tang D,et al.KCNE2 protein is expressed in ventricles of different species,and changes in its expression contribute to electrical remodeling in diseased hearts[J].Circulation,2004,109(14):1783-8.

共引文献4

同被引文献3

引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部