Inactivation kinetics of voltage-gated calcium channels in glutamatergic neurons are influenced by SNAP-25

被引:13
作者
Condliffe, Steven B. [1 ]
Matteoli, Michela [2 ,3 ]
机构
[1] Univ Otago, Dept Physiol, Dunedin, New Zealand
[2] Univ Milan, Dept Med Pharmacol, CNR Inst Neurosci, Milan, Italy
[3] Univ Milan, IRCCS Don Gnocchi, Milan, Italy
关键词
voltage-gated calcium channels; SNAP-25; inactivation; kinetics; hippocampal neurons; glutamatergic; GABAergic; CA(V)2.1 CHANNELS; CA2+ CHANNELS; MODULATION; SYNTAXIN;
D O I
10.4161/chan.5.4.16228
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
SNAP-25 forms part of the SNARE core complex that mediates membrane fusion. Biochemical and electrophysiological evidence supports an accessory role for SNAP-25 in interacting with voltage-gated calcium channels (VGCCs) to modulate channel activity. We recently reported that endogenous SNAP-25 negatively regulates VGCC activity in glutamatergic neurons from rat hippocampal cultures by shifting the voltage-dependence of inactivation of the predominant P/Q-type channel current in these cells. In the present study, we extend these findings by investigating the effect that manipulating endogenous SNAP-25 expression has on the inactivation kinetics of VGCC current in both glutamatergic and GABAergic cells recorded from 9-13 DIV cultures. Silencing SNAP-25 in glutamatergic neurons significantly slowed the inactivation rate of P/Q-type VGCC current whereas alterations in SNAP-25 expression did not alter inactivation rates in GABAergic neurons. These results indicate that endogenous SNAP-25 plays an important role in P/Q-type channel regulation in glutamatergic neurons.
引用
收藏
页码:304 / 307
页数:4
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