Neuronal Calcium Wave Propagation Varies with Changes in Endoplasmic Reticulum Parameters: A Computer Model

摘要

Calcium () waves provide a complement to neuronal electrical signaling, forming a key part of a neuron’s second messenger system. We developed a reaction-diffusion model of an apical dendrite with diffusible inositol triphosphate (), diffusible , receptors (s), endoplasmic reticulum (ER) leak, and ER pump (SERCA) on ER. is released from ER stores via s upon binding of and . This results in -induced--release (CICR) and increases spread. At least two modes of wave spread have been suggested: a continuous mode based on presumed relative homogeneity of ER within the cell and a pseudo-saltatory model where regeneration occurs at discrete points with - iffusion between them. We compared the effects of three patterns of hypothesized distribution: (1) continuous homogeneous ER, (2) hotspots with increased density ( hotspots), and (3) areas of increased ER density (ER stacks). All three modes produced waves with velocities similar to those measured in vitro (approximately 50–90 m /sec). Continuous ER showed high sensitivity to density increases, with time to onset reduced and speed increased. Increases in SERCA density resulted in opposite effects. The measures were sensitive to changes in density and spacing of hotspots and stacks. Increasing the apparent diffusion coefficient of   substantially increased wave speed. An extended electrochemical model, including voltage-gated calcium channels and AMPA synapses, demonstrated that membrane priming via AMPA stimulation enhances subsequent wave amplitude and duration. Our modeling suggests that pharmacological targeting of s and SERCA could allow modulation of wave propagation in diseases w