Wagner J, Keizer J
Institute of Theoretical Dynamics, University of California, Davis 95616.
Biophys J. 1994 Jul;67(1):447-56. doi: 10.1016/S0006-3495(94)80500-4.
Based on realistic mechanisms of Ca2+ buffering that include both stationary and mobile buffers, we derive and investigate models of Ca2+ diffusion in the presence of rapid buffers. We obtain a single transport equation for Ca2+ that contains the effects caused by both stationary and mobile buffers. For stationary buffers alone, we obtain an expression for the effective diffusion constant of Ca2+ that depends on local Ca2+ concentrations. Mobile buffers, such as fura-2, BAPTA, or small endogenous proteins, give rise to a transport equation that is no longer strictly diffusive. Calculations are presented to show that these effects can modify greatly the manner and rate at which Ca2+ diffuses in cells, and we compare these results with recent measurements by Allbritton et al. (1992). As a prelude to work on Ca2+ waves, we use a simplified version of our model of the activation and inhibition of the IP3 receptor Ca2+ channel in the ER membrane to illustrate the way in which Ca2+ buffering can affect both the amplitude and existence of Ca2+ oscillations.
基于包括固定缓冲剂和移动缓冲剂在内的现实的Ca2+缓冲机制,我们推导并研究了在快速缓冲剂存在下Ca2+扩散的模型。我们得到了一个包含固定缓冲剂和移动缓冲剂所引起效应的Ca2+单一传输方程。仅对于固定缓冲剂,我们得到了一个依赖于局部Ca2+浓度的Ca2+有效扩散常数的表达式。移动缓冲剂,如fura-2、BAPTA或小的内源性蛋白质,会产生一个不再严格扩散的传输方程。计算结果表明,这些效应可以极大地改变Ca2+在细胞内扩散的方式和速率,并且我们将这些结果与Allbritton等人(1992年)最近的测量结果进行了比较。作为研究Ca2+波的前奏,我们使用内质网膜中IP3受体Ca2+通道激活和抑制模型的简化版本,来说明Ca2+缓冲如何影响Ca2+振荡的幅度和存在情况。