Marth Wieland, Voigt Axel
Department of Mathematics, TU Dresden, 01062 , Dresden, Germany,
J Math Biol. 2014 Jul;69(1):91-112. doi: 10.1007/s00285-013-0704-4. Epub 2013 Jul 9.
The processes of protrusion and retraction during cell movement are driven by the turnover and reorganization of the actin cytoskeleton. Within a reaction-diffusion model which combines processes along the cell membrane with processes within the cytoplasm a Turing type instability is used to form the necessary polarity to distinguish between cell front and rear and to initiate the formation of different organizational arrays within the cytoplasm leading to protrusion and retraction. A simplified biochemical network model for the activation of GTPase which accounts for the different dimensionality of the cell membrane and the cytoplasm is used for this purpose and combined with a classical Helfrich type model to account for bending and stiffness effects of the cell membrane. In addition streaming within the cytoplasm and the extracellular matrix is taken into account. Combining these phenomena allows to simulate the dynamics of cells and to reproduce the primary phenomenology of cell motility. The coupled model is formulated within a phase field approach and solved using adaptive finite elements.
细胞运动过程中的突出和回缩过程是由肌动蛋白细胞骨架的周转和重组驱动的。在一个反应扩散模型中,该模型将细胞膜上的过程与细胞质内的过程相结合,利用图灵型不稳定性来形成区分细胞前端和后端的必要极性,并启动细胞质内不同组织阵列的形成,从而导致突出和回缩。为此,使用了一个简化的用于激活GTP酶的生化网络模型,该模型考虑了细胞膜和细胞质的不同维度,并与经典的赫尔弗里希型模型相结合,以考虑细胞膜的弯曲和刚度效应。此外,还考虑了细胞质和细胞外基质内的流动。将这些现象结合起来可以模拟细胞的动态,并重现细胞运动的主要现象学。耦合模型是在相场方法中制定的,并使用自适应有限元求解。