Iacobas Dumitru A, Suadicani Sylvia O, Spray David C, Scemes Eliana
Department of Neuroscience, Albert Einstein College of Medicine, Bronx, New York, USA.
Biophys J. 2006 Jan 1;90(1):24-41. doi: 10.1529/biophysj.105.064378. Epub 2005 Oct 7.
We describe a two-dimensional stochastic model of intercellular Ca(2+) wave (ICW) spread in glia that includes contributions of external stimuli, ionotropic and metabotropic P2 receptors, exo- and ecto-nucleotidases, second messengers, and gap junctions. In this model, an initial stimulus evokes ATP and UTP release from a single cell. Agonists diffuse and are degraded both in bulk solution and at cell surfaces. Ca(2+) elevation in individual cells is determined by bound agonist concentrations s and by number and features of P2 receptors summed with that generated by IP(3) diffusing through gap junction channels. Variability of ICWs is provided by randomly distributing a predetermined density of cells in a rectangular grid and by randomly selecting within intervals values characterizing the extracellular compartment, individual cells, and interconnections with neighboring cells. Variability intervals were obtained from experiments on astrocytoma cells transfected to express individual P2 receptors and/or the gap junction protein connexin43. The simulation program (available as Supplementary Material) permits individual alteration of ICW components, allowing comparison of simulations with data from cells expressing connexin43 and/or various P2 receptor subtypes. Such modeling is expected to be useful for testing phenomenological hypotheses and in understanding consequences of alteration of system components under experimental or pathological conditions.
我们描述了一种二维随机模型,用于模拟神经胶质细胞中细胞间Ca(2+)波(ICW)的传播,该模型考虑了外部刺激、离子型和代谢型P2受体、胞外和胞外核苷酸酶、第二信使以及缝隙连接的作用。在这个模型中,初始刺激会引发单个细胞释放ATP和UTP。激动剂在体溶液和细胞表面扩散并降解。单个细胞内Ca(2+)的升高由结合的激动剂浓度s以及P2受体的数量和特性决定,再加上通过缝隙连接通道扩散的IP(3)所产生的Ca(2+)升高。ICW的变异性是通过在矩形网格中随机分布预定密度的细胞,以及在区间内随机选择表征细胞外区室、单个细胞和与相邻细胞连接的数值来实现的。变异性区间来自对转染以表达单个P2受体和/或缝隙连接蛋白连接蛋白43的星形细胞瘤细胞的实验。模拟程序(作为补充材料提供)允许对ICW组件进行单独更改,从而能够将模拟结果与来自表达连接蛋白43和/或各种P2受体亚型的细胞的数据进行比较。这种建模预计将有助于检验现象学假设,并理解在实验或病理条件下系统组件改变的后果。