Mathematical modelling of fluid transport and its regulation at multiple scales

被引:5
作者
Chara, Osvaldo [1 ,2 ,3 ]
Brusch, Lutz [3 ]
机构
[1] Consejo Nacl Invest Cient & Tecn, Inst Phys Liquids & Biol Syst IFLYSIB, RA-1900 La Plata, Buenos Aires, Argentina
[2] Natl Univ La Plata, RA-1900 La Plata, Buenos Aires, Argentina
[3] Tech Univ Dresden, Ctr Informat Serv & High Performance Comp, D-01069 Dresden, Germany
关键词
Osmosis; Cell volume homeostasis; Cyst lumen; Mathematical model; CELL-VOLUME REGULATION; ATP RELEASE; GOLDFISH HEPATOCYTES; MECHANISMS; FEEDBACK; MORPHOGENESIS; LOCALIZATION; PERMEABILITY; INTEGRATION; EPITHELIA;
D O I
10.1016/j.biosystems.2015.02.004
中图分类号
Q [生物科学];
学科分类号
090105 [作物生产系统与生态工程];
摘要
Living matter equals water, to a first approximation, and water transport across barriers such as membranes and epithelia is vital. Water serves two competing functions. On the one hand, it is the fundamental solvent enabling random mobility of solutes and therefore biochemical reactions and intracellular signal propagation. Homeostasis of the intracellular water volume is required such that messenger concentration encodes the stimulus and not inverse volume fluctuations. On the other hand, water flow is needed for transport of solutes to and away from cells in a directed manner, threatening volume homeostasis and signal transduction fidelity of cells. Feedback regulation of fluid transport reconciles these competing objectives. The regulatory mechanisms often span across multiple spatial scales from cellular interactions up to the architecture of organs. Open questions relate to the dependency of water fluxes and steady state volumes on control parameters and stimuli. We here review selected mathematical models of feedback regulation of fluid transport at the cell scale and identify a general "core shell" structure of such models. We propose that fluid transport models at other spatial scales can be constructed in a generalised core-shell framework, in which the core accounts for the biophysical effects of fluid transport whilst the shell reflects the regulatory mechanisms. We demonstrate the applicability of this framework for tissue lumen growth and suggest future experiments in zebrafish to test lumen size regulation mechanisms. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:1 / 10
页数:10
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