Fardin M A, Rossier O M, Rangamani P, Avigan P D, Gauthier N C, Vonnegut W, Mathur A, Hone J, Iyengar R, Sheetz M P
Department of Biological Sciences, Fairchild Building Columbia University, New York, NY 10027, USA.
Soft Matter. 2010 Aug 10;6:4788-4799. doi: 10.1039/c0sm00252.
Many cell types have the ability to move themselves by crawling on extra-cellular matrices. Although cell motility is governed by actin and myosin filament assembly, the pattern of the movement follows the physical properties of the network ensemble average. The first step of motility, cell spreading on matrix substrates, involves a transition from round cells in suspension to polarized cells on substrates. Here we show that the spreading dynamics on 2D surfaces can be described as a hydrodynamic process. In particular, we show that the transition from isotropic spreading at early time to anisotropic spreading is reminiscent of the fingering instability observed in many spreading fluids. During cell spreading, the main driving force is the polymerization of actin filaments that push the membrane forward. From the equilibrium between the membrane force and the cytoskeleton, we derive a first order expression of the polymerization stress that reproduces the observed behavior. Our model also allows an interpretation of the effects of pharmacological agents altering the polymerization of actin. In particular we describe the influence of Cytochalasin D on the nucleation of the fingering instability.
许多细胞类型能够通过在细胞外基质上爬行来移动自身。尽管细胞运动受肌动蛋白和肌球蛋白丝组装的控制,但运动模式遵循网络集合平均值的物理特性。运动的第一步,即细胞在基质底物上的铺展,涉及从悬浮的圆形细胞到底物上极化细胞的转变。在这里,我们表明二维表面上的铺展动力学可以描述为一个流体动力学过程。特别是,我们表明从早期的各向同性铺展到各向异性铺展的转变让人联想到在许多铺展流体中观察到的指进不稳定性。在细胞铺展过程中,主要驱动力是推动膜向前的肌动蛋白丝的聚合。从膜力和细胞骨架之间的平衡出发,我们推导出了聚合应力的一阶表达式,该表达式再现了观察到的行为。我们的模型还允许解释改变肌动蛋白聚合的药理剂的作用。特别是,我们描述了细胞松弛素D对指进不稳定性成核的影响。