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
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