Hinch R, Greenstein J L, Tanskanen A J, Xu L, Winslow R L
Mathematical Institute, University of Oxford, Oxford, United Kingdom.
Biophys J. 2004 Dec;87(6):3723-36. doi: 10.1529/biophysj.104.049973. Epub 2004 Oct 1.
Calcium (Ca2+)-induced Ca2+ release (CICR) in cardiac myocytes exhibits high gain and is graded. These properties result from local control of Ca2+ release. Existing local control models of Ca2+ release in which interactions between L-Type Ca2+ channels (LCCs) and ryanodine-sensitive Ca2+ release channels (RyRs) are simulated stochastically are able to reconstruct these properties, but only at high computational cost. Here we present a general analytical approach for deriving simplified models of local control of CICR, consisting of low-dimensional systems of coupled ordinary differential equations, from these more complex local control models in which LCC-RyR interactions are simulated stochastically. The resulting model, referred to as the coupled LCC-RyR gating model, successfully reproduces a range of experimental data, including L-Type Ca2+ current in response to voltage-clamp stimuli, inactivation of LCC current with and without Ca2+ release from the sarcoplasmic reticulum, voltage-dependence of excitation-contraction coupling gain, graded release, and the force-frequency relationship. The model does so with low computational cost.
心肌细胞中的钙(Ca2+)诱导的钙释放(CICR)具有高增益且呈分级性。这些特性源于钙释放的局部调控。现有的钙释放局部调控模型,其中L型钙通道(LCCs)和雷诺丁敏感钙释放通道(RyRs)之间的相互作用是随机模拟的,能够重构这些特性,但计算成本很高。在此,我们提出一种通用的分析方法,用于从这些更复杂的、随机模拟LCC-RyR相互作用的局部调控模型中推导简化的CICR局部调控模型,该简化模型由耦合常微分方程的低维系统组成。所得模型,称为耦合LCC-RyR门控模型,成功再现了一系列实验数据,包括电压钳刺激下的L型钙电流、有无肌浆网钙释放时LCC电流的失活、兴奋-收缩偶联增益的电压依赖性、分级释放以及力-频率关系。该模型以低计算成本做到了这一点。