(R)-ROSCOVITINE PROLONGS THE MEAN OPEN TIME OF UNITARY N-TYPE CALCIUM CHANNEL CURRENTS

被引:22
作者
DeStefino, N. R. [1 ,2 ]
Pilato, A. A. [1 ,2 ]
Dittrich, M. [3 ]
Cherry, S. V. [1 ,2 ]
Cho, S. [1 ,2 ]
Stiles, J. R. [1 ,2 ,3 ,4 ]
Meriney, S. D. [1 ,2 ]
机构
[1] Univ Pittsburgh, Dept Neurosci, Pittsburgh, PA 15260 USA
[2] Univ Pittsburgh, Ctr Neurosci, Pittsburgh, PA 15260 USA
[3] Pittsburgh Supercomp Ctr, Pittsburgh, PA 15213 USA
[4] Carnegie Mellon Univ, Dept Biol Sci, Pittsburgh, PA 15213 USA
基金
美国国家科学基金会;
关键词
voltage-gated calcium channel; patch clamp; roscovitine; single channel current; channel kinetics; conductance; G-PROTEIN INHIBITION; TRANSMITTER RELEASE; NEUROTRANSMITTER RELEASE; PRESYNAPTIC CALCIUM; SINGLE CHANNELS; CA-CHANNELS; OPEN-STATE; VOLTAGE; MODULATION; ROSCOVITINE;
D O I
10.1016/j.neuroscience.2010.02.041
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
(R)-roscovitine (Ros) is a cyclin-dependent kinase inhibitor that also has been shown to have direct agonist and antagonist actions on Ca(v)2.1 (P/Q-type) and Ca-v 2.2 (N-type) families of voltage-gated calcium channels. These kinase-independent effects represent a novel opportunity to advance our understanding of calcium channel function and calcium-triggered neurotransmitter release. Furthermore, such actions on calcium channels may direct the development of Ros derivatives as new therapeutic agents. We used patch clamp recordings to characterize mechanisms that underlie the agonist effects of Ros on unitary N-type calcium channel gating. We found that N-type channels normally gate with either a short or long mean open time, that Ros significantly prolonged the mean open time of the long gating component and increased the probability of observing channels that gated with a long open time, but had no effect on single channel conductance. Using Monte Carlo simulations of a single channel kinetic model and Ros interactions, we were able to reproduce our experimental results and investigate the model's microscopic dynamics. In particular, our simulations predicted that the longer open times generated by Ros were due to the appearance of a long open state combined with an increased amount of time spent in transitions between open states. Our results suggest a mechanism for agonist effects of Ros at the level of single channels, and provide a mechanistic explanation for previously reported agonist effects on whole cell calcium currents. (C) 2010 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:838 / 849
页数:12
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