G-protein modulation of N-type calcium channel gating current in human embryonic kidney cells (HEK 293)

被引:55
作者
Jones, LP
Patil, PG
Snutch, TP
Yue, DT
机构
[1] JOHNS HOPKINS UNIV,SCH MED,DEPT BIOMED ENGN,PROGRAM MOL & CELLULAR SYST PHYSIOL,BALTIMORE,MD 21205
[2] UNIV BRITISH COLUMBIA,VANCOUVER,BC V6T 173,CANADA
来源
JOURNAL OF PHYSIOLOGY-LONDON | 1997年 / 498卷 / 03期
关键词
D O I
10.1113/jphysiol.1997.sp021886
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
1. Voltage-dependent inhibition of N-type calcium currents by G-proteins contributes importantly to presynaptic inhibition. To examine the effect of G-proteins on key intermediary transitions leading to channel opening, we measured both gating and ionic currents arising from recombinant N-type channels (alpha(1B), beta(1b) and alpha(2)) expressed in transiently transfected human embryonic kidney cells (HEK 293). Recombinant expression population of channels provided a favourable system for rigorous examination of the mechanisms underlying G-protein modulation. 2. During intracellular dialysis with GTP gamma S to activate G-proteins, ionic currents demonstrated classic features of voltage-dependent inhibition, i.e. strong depolarizing prepulses increased ionic currents and produced hyperpolarizing shifts in the voltage-dependent activation of ionic current. No such effects were observed with GDP beta S present to minimize G-protein activity. 3. Gating currents were clearly resolved after ionic current blockade with 0.1. mM free La3+, enabling this first report of gating charge translocation arising exclusively from N-type channels. G-proteins decreased the amplitude of gating currents and produced depolarizing shifts in the voltage-dependent activation of gating charge movement. However, the greatest effect was to induce a similar to 20 mV separation between the voltage-dependent activation of gating charge movement and ionic current. Strong depolarizing prepulses largely reversed these effects. These modulatory features provide telling clues about the kinetic steps affected by G-proteins because gating currents arise from the movement of voltage sensors that trigger channel activation. 4. The mechanistic implications of concomitant G-protein-mediated changes in gating and ionic currents are discussed. We argue that G-proteins act to inhibit both voltage-sensor movement and the transduction of voltage-sensor activation into channel opening.
引用
收藏
页码:601 / 610
页数:10
相关论文
共 33 条
  • [1] CHARGE MOVEMENT ASSOCIATED WITH OPENING AND CLOSING OF ACTIVATION GATES OF NA CHANNELS
    ARMSTRONG, CM
    BEZANILLA, F
    [J]. JOURNAL OF GENERAL PHYSIOLOGY, 1974, 63 (05) : 533 - 552
  • [2] SODIUM-CHANNELS AND GATING CURRENTS
    ARMSTRONG, CM
    [J]. PHYSIOLOGICAL REVIEWS, 1981, 61 (03) : 644 - 683
  • [3] BEAN BP, 1990, BIOPHYS J, V57, pA23
  • [4] NONLINEAR CHARGE MOVEMENT IN MAMMALIAN CARDIAC VENTRICULAR CELLS - COMPONENTS FROM NA AND CA CHANNEL GATING
    BEAN, BP
    RIOS, E
    [J]. JOURNAL OF GENERAL PHYSIOLOGY, 1989, 94 (01) : 65 - 93
  • [6] Endogenous calcium channels in human embryonic kidney (HEK293) cells
    Berjukow, S
    Doring, F
    Froschmayr, M
    Grabner, M
    Glossmann, H
    Hering, S
    [J]. BRITISH JOURNAL OF PHARMACOLOGY, 1996, 118 (03) : 748 - 754
  • [7] BOLAND LM, 1993, J NEUROSCI, V13, P516
  • [8] Determinants of the G protein-dependent opioid modulation of neuronal calcium channels
    Bourinet, E
    Soong, TW
    Stea, A
    Snutch, TP
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (04) : 1486 - 1491
  • [9] HUMAN NEURONAL VOLTAGE-DEPENDENT CALCIUM CHANNELS - STUDIES ON SUBUNIT STRUCTURE AND ROLE IN CHANNEL ASSEMBLY
    BRUST, PF
    SIMERSON, S
    MCCUE, AF
    DEAL, CR
    SCHOONMAKER, S
    WILLIAMS, ME
    VELICELEBI, G
    JOHNSON, EC
    HARPOLD, MM
    ELLIS, SB
    [J]. NEUROPHARMACOLOGY, 1993, 32 (11) : 1089 - 1102
  • [10] A NEW SUBUNIT OF THE CYCLIC NUCLEOTIDE-GATED CATION CHANNEL IN RETINAL RODS
    CHEN, TY
    PENG, YW
    DHALLAN, RS
    AHAMED, B
    REED, RR
    YAU, KW
    [J]. NATURE, 1993, 362 (6422) : 764 - 767