Hybrid Stochastic and deterministic Simulations of calcium blips

被引:87
作者
Ruediger, S. [1 ]
Shuai, J. W.
Huisinga, W.
Nagaiah, C.
Warnecke, G.
Parker, I.
Falcke, M.
机构
[1] Humboldt Univ, Inst Phys, Berlin, Germany
[2] Hahn Meitner Inst Berlin GmbH, D-1000 Berlin, Germany
[3] Univ Calif Irvine, Dept Neurobiol & Behav, Irvine, CA USA
[4] Dept Math & Comp Sci, Berlin, Germany
[5] NUIM, Hamilton Inst, Maynooth, Kildare, Ireland
[6] Otto Von Guericke Univ, Inst Anal & Numer Math, Magdeburg, Germany
关键词
INOSITOL 1,4,5-TRISPHOSPHATE RECEPTOR; INTRACELLULAR CA2+; IP3; RECEPTORS; SPATIAL-DISTRIBUTION; SIGNALING SYSTEM; OSCILLATIONS; CHANNEL; SINGLE; MODEL; DIFFUSION;
D O I
10.1529/biophysj.106.099879
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Intracellular calcium release is a prime example for the role of stochastic effects in cellular systems. Recent models consist of deterministic reaction-diffusion equations coupled to stochastic transitions of calcium channels. The resulting dynamics is of multiple time and spatial scales, which complicates far-reaching computer simulations. In this article, we introduce a novel hybrid scheme that is especially tailored to accurately trace events with essential stochastic variations, while deterministic concentration variables are efficiently and accurately traced at the same time. We use finite elements to efficiently resolve the extreme spatial gradients of concentration variables close to a channel. We describe the algorithmic approach and we demonstrate its efficiency compared to conventional methods. Our single-channel model matches experimental data and results in intriguing dynamics if calcium is used as charge carrier. Random openings of the channel accumulate in bursts of calcium blips that may be central for the understanding of cellular calcium dynamics.
引用
收藏
页码:1847 / 1857
页数:11
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