Department of Mathematics, University of British Columbia, Vancouver, BC, V6T 1Z2, Canada.
Bull Math Biol. 2020 Feb 3;82(2):28. doi: 10.1007/s11538-020-00702-5.
Cell polarization requires redistribution of specific proteins to the nascent front and back of a eukaryotic cell. Among these proteins are Rac and Rho, members of the small GTPase family that regulate the actin cytoskeleton. Rac promotes actin assembly and protrusion of the front edge, whereas Rho activates myosin-driven contraction at the back. Mathematical models of cell polarization at many levels of detail have appeared. One of the simplest based on "wave-pinning" consists of a pair of reaction-diffusion equations for a single GTPase. Mathematical analysis of wave-pinning so far is largely restricted to static domains in one spatial dimension. Here, we extend the analysis to cells that change in size, showing that both shrinking and growing cells can lose polarity. We further consider the feedback between mechanical tension, GTPase activation, and cell deformation in both static, growing, shrinking, and moving cells. Special cases (spatially uniform cell chemistry, the absence or presence of mechanical feedback) are analyzed, and the full model is explored by simulations in 1D. We find a variety of novel behaviors, including "dilution-induced" oscillations of Rac activity and cell size, as well as gain or loss of polarization and motility in the model cell.
细胞极化需要将特定蛋白质重新分配到真核细胞的新前端和后端。这些蛋白质包括 Rac 和 Rho,它们是调节肌动蛋白细胞骨架的小 GTPase 家族的成员。Rac 促进肌动蛋白组装和前端的突出,而 Rho 则激活肌球蛋白驱动的后端收缩。已经出现了许多细节水平的细胞极化数学模型。其中最简单的基于“波钉扎”的模型由一对用于单个 GTPase 的反应扩散方程组成。到目前为止,波钉扎的数学分析主要限于一维空间中的静态域。在这里,我们将分析扩展到大小发生变化的细胞,表明收缩和生长的细胞都可能失去极性。我们进一步考虑了在静态、生长、收缩和运动细胞中机械张力、GTPase 激活和细胞变形之间的反馈。分析了特殊情况(空间均匀的细胞化学、机械反馈的存在或不存在),并通过一维模拟探索了完整模型。我们发现了各种新的行为,包括 Rac 活性和细胞大小的“稀释诱导”振荡,以及模型细胞中极化和迁移能力的获得或丧失。