Modelling of simple and complex calcium oscillations -: From single-cell responses to intercellular signalling

被引:305
作者
Schuster, S
Marhl, M
Höfer, T
机构
[1] Max Delbruck Ctr Mol Med, Dept Bioinformat, D-13092 Berlin, Germany
[2] Humboldt Univ, Inst Biol, Berlin, Germany
[3] Univ Maribor, Fac Educ, Dept Phys, SLO-2000 Maribor, Slovenia
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 2002年 / 269卷 / 05期
关键词
bursting; calcium-induced calcium release; calcium oscillations; entrainment; frequency encoding; gap junctions; Hopf bifurcation; homoclinic bifurcation; inositol 1,4,5-trisphosphate; IP3; receptors;
D O I
10.1046/j.0014-2956.2001.02720.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This review provides a comparative overview of recent developments in the modelling of cellular calcium oscillations. A large variety of mathematical models have been developed for this wide-spread phenomenon in intra- and intercellular signalling. From these, a general model is extracted that involves six types of concentration variables: inositol 1,4,5-trisphosphate (IP3), cytoplasmic, endoplasmic reticulum and mitochondrial calcium, the occupied binding sites of calcium buffers, and the fraction of active IP3 receptor calcium release channels. Using this framework, the models of calcium oscillations can be classified into 'minimal' models containing two variables and 'extended' models of three and more variables. Three types of minimal models are identified that are all based on calcium-induced calcium release (CICR), but differ with respect to the mechanisms limiting CICR. Extended models include IP3-calcium cross-coupling, calcium sequestration by mitochondria, the detailed gating kinetics of the IP3 receptor, and the dynamics of G-protein activation. In addition to generating regular oscillations, such models can describe bursting and chaotic calcium dynamics. The earlier hypothesis that information in calcium oscillations is encoded mainly by their frequency is nowadays modified in that some effect is attributed to amplitude encoding or temporal encoding. This point is discussed with reference to the analysis of the local and global bifurcations by which calcium oscillations can arise. Moreover, the question of how calcium binding proteins can sense and transform oscillatory signals is addressed. Recently, potential mechanisms leading to the coordination of oscillations in coupled cells have been investigated by mathematical modelling. For this, the general modelling framework is extended to include cytoplasmic and gap functional diffusion of IP3 and calcium, and specific models are compared. Various suggestions concerning the physiological significance of oscillatory behaviour in intra- and intercellular signalling are discussed. The article is concluded with a discussion of obstacles and prospects.
引用
收藏
页码:1333 / 1355
页数:23
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