[3H]Dofetilide binding in SHSY5Y and HEK293 cells expressing a HERG-like K+ channel?

被引:32
作者
Finlayson, K [1 ]
Pennington, AJ [1 ]
Kelly, JS [1 ]
机构
[1] Univ Edinburgh, Dept Neurosci, Fujisawa Inst Neurosci, Edinburgh EH8 9JZ, Midlothian, Scotland
关键词
H-3]dofetilide binding; SHSY5Y cell; HEK293; cell; CHO-K1; HERG (human ether-a-gogo-related gene); RT-PCR (reverse transcriptasepolymerase; chain reaction);
D O I
10.1016/S0014-2999(01)00731-2
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The pharmacological characteristics of [H-3]dofetilide binding in SHSY5Y, HEK293 and CHO-K1 cells were examined, and in parallel whole cell recordings used to characterise HERG-like K+ currents. Dofetilide affinity was similar in the human cell lines, SHSY5Y (K-d = 99.6 nM) and HEK293 ( K-d = 102.9 nM), but 10 times lower in CHO-K1 cells (K-d = 1200 nM). In contrast, clofilium and E4031 had a similar affinity in all three cell lines, whereas WAY 123,398 had no effect. Electrophysiological studies showed that SHSY5Y cells contained a HERG-like K+ current blocked by application of dofetilide to either side of the membrane. Block was faster when dofetilide was applied intracellularly. In contrast, HEK293 and CHO-K1 cells contained no such current, despite the presence of a partial cDNA for HERG in the former. That [H-3]dofetilide is specific for I-Kr/HERG may be questionable, as HEK293 and CHO-K1 cells contain no such functional K+ current. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:203 / 212
页数:10
相关论文
共 36 条
  • [1] Long term exposure to retinoic acid induces the expression of IRK1 channels in HERG channel-endowed neuroblastoma cells
    Arcangeli, A
    Rosati, B
    Cherubini, A
    Crociani, O
    Fontana, L
    Passani, B
    Wanke, E
    Olivotto, M
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 244 (03) : 706 - 711
  • [2] A novel inward-rectifying K+ current with a cell-cycle dependence governs the resting potential of mammalian neuroblastoma cells
    Arcangeli, A
    Bianchi, L
    Becchetti, A
    Faravelli, L
    Coronnello, M
    Mini, E
    Olivotto, M
    Wanke, E
    [J]. JOURNAL OF PHYSIOLOGY-LONDON, 1995, 489 (02): : 455 - 471
  • [3] Bianchi L, 1998, CANCER RES, V58, P815
  • [4] IDENTIFICATION OF A SPECIFIC RADIOLIGAND FOR THE CARDIAC RAPIDLY ACTIVATING DELAYED RECTIFIER K+ CHANNEL
    CHADWICK, CC
    EZRIN, AM
    OCONNOR, B
    VOLBERG, WA
    SMITH, DI
    WEDGE, KJ
    HILL, RJ
    BRIGGS, GM
    PAGANI, ED
    SILVER, PJ
    KRAFTE, DS
    [J]. CIRCULATION RESEARCH, 1993, 72 (03) : 707 - 714
  • [5] CHENG Y, 1973, BIOCHEM PHARMACOL, V22, P3099
  • [6] A novel role for HERG K+ channels: Spike-frequency adaptation
    Chiesa, N
    Rosati, B
    Arcangeli, A
    Olivotto, M
    Wanke, E
    [J]. JOURNAL OF PHYSIOLOGY-LONDON, 1997, 501 (02): : 313 - 318
  • [7] [H-3]dofetilide binding to cardiac myocytes: Modulation by extracellular potassium
    Duff, HJ
    Feng, ZP
    Fiset, C
    Wang, L
    LeesMiller, J
    Sheldon, RS
    [J]. JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1997, 29 (01) : 183 - 191
  • [8] HIGH- AND LOW-AFFINITY SITES FOR [H-3] DOFETILIDE BINDING TO GUINEA-PIG MYOCYTES
    DUFF, HJ
    FENG, ZP
    SHELDON, RS
    [J]. CIRCULATION RESEARCH, 1995, 77 (04) : 718 - 725
  • [9] Regulation of expression of the [H-3]-dofetilide binding site associated with the delayed rectifier K+ channel by dexamethasone in neonatal mouse ventricle
    Duff, HJ
    Feng, ZP
    Wang, L
    Sheldon, RS
    [J]. JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1997, 29 (07) : 1959 - 1965
  • [10] A HERG-like K+ channel in rat F-11 DRG cell line: Pharmacological identification and biophysical characterization
    Faravelli, L
    Arcangeli, A
    Olivotto, M
    Wanke, E
    [J]. JOURNAL OF PHYSIOLOGY-LONDON, 1996, 496 (01): : 13 - 23