Helmchen Fritjof, Tank David W
Cold Spring Harb Protoc. 2015 Feb 2;2015(2):155-67. doi: 10.1101/pdb.top085910.
This introduction describes a single-compartment model of calcium dynamics that has been applied to fluorescence measurements of intracellular free calcium concentration ([Ca(2+)]i) changes in neurons. The model describes intracellular calcium handling under simplified conditions, for which analytical expressions for the amplitude and the time constants of [Ca(2+)]i changes can be explicitly derived. In particular, it reveals the dependence of the measured [Ca(2+)]i changes on the calcium indicator concentration. Applied to experimental data from small cells or subcellular compartments, the model equations have been extremely useful for obtaining quantitative information about essential parameters of Ca(2+) influx, buffering, and clearance. We illustrate also several changes that occur when the basic assumptions do not hold (e.g., when calcium diffusion, dye saturation, or kinetic effects become significant). Finally, we discuss how the changes in calcium dynamics, which are explained by the model, have been exploited for measuring properties of calcium-driven reactions, such as those regulating short-term synaptic enhancement, vesicle recycling, and adaptation.
本引言描述了一种钙动力学单室模型,该模型已应用于神经元细胞内游离钙浓度([Ca(2+)]i)变化的荧光测量。该模型描述了简化条件下的细胞内钙处理过程,据此可以明确推导出[Ca(2+)]i变化的幅度和时间常数的解析表达式。特别是,它揭示了测得的[Ca(2+)]i变化对钙指示剂浓度的依赖性。将该模型方程应用于来自小细胞或亚细胞区室的实验数据,对于获取有关Ca(2+)内流、缓冲和清除等基本参数的定量信息极为有用。我们还说明了当基本假设不成立时(例如,当钙扩散、染料饱和或动力学效应变得显著时)会发生的几种变化。最后,我们讨论了该模型所解释的钙动力学变化是如何被用于测量钙驱动反应的特性的,比如那些调节短期突触增强、囊泡循环和适应性的反应。