Evans E
Department of Pathology, University of British Columbia, Vancouver, Canada.
Biophys J. 1993 Apr;64(4):1306-22. doi: 10.1016/S0006-3495(93)81497-8.
Amoeboid motion of cells is an essential mechanism in the function of many biological organisms (e.g., the regiment of scavenger cells in the immune defense system of animals). This process involves rapid chemical polymerization (with numerous protein constituents) to create a musclelike contractile network that advances the cell over the surface. Significant progress has been made in the biology and biochemistry of motile cells, but the physical dynamics of cell spreading and contraction are not well understood. The reason is that general approaches are formulated from complex mass, momentum, and chemical reaction equations for multiphase-multicomponent flow with the nontrivial difficulty of moving boundaries. However, there are strong clues to the dynamics that allow bold steps to be taken in simplifying the physics of motion. First, amoeboid cells often exhibit exceptional kinematics, i.e., steady advance and retraction of local fixed-shape patterns. Second, recent evidence has shown that cell projections "grow" by polymerization along the advancing boundary of the cell. Together, these characteristics represent a local growth process pinned to the interfacial contour of a contractile network. As such, the moving boundary becomes tractable, but subtle features of the motion lead to specific requirements for the chemical nature of the boundary polymerization process. To demonstrate these features, simple examples for limiting conditions of substrate interaction (i.e., "strong" and "weak" adhesion) are compared with data from experimental studies of yeast particle engulfment by blood granulocytes and actin network dynamics in fishscale keratocytes.
细胞的阿米巴样运动是许多生物机体功能中的一种基本机制(例如,动物免疫防御系统中吞噬细胞的聚集)。这个过程涉及快速的化学聚合反应(有众多蛋白质成分参与),以形成一个类似肌肉的收缩网络,使细胞在表面向前移动。在运动细胞的生物学和生物化学方面已经取得了重大进展,但细胞铺展和收缩的物理动力学尚未得到很好的理解。原因在于,一般方法是根据多相多组分流动的复杂质量、动量和化学反应方程制定的,存在移动边界这一 nontrivial 难题。然而,动力学方面有一些有力线索,使得我们能够大胆地简化运动物理学。首先,阿米巴样细胞常常表现出特殊的运动学特征,即局部固定形状模式的稳定前进和后退。其次,最近的证据表明,细胞突起通过沿着细胞前进边界的聚合作用而“生长”。这些特征共同构成了一个固定在收缩网络界面轮廓上的局部生长过程。这样一来,移动边界变得易于处理,但运动的微妙特征对边界聚合过程的化学性质提出了特定要求。为了展示这些特征,将底物相互作用限制条件(即“强”和“弱”黏附)的简单示例与血液粒细胞吞噬酵母颗粒的实验研究数据以及鱼鳞角质形成细胞中的肌动蛋白网络动力学数据进行了比较。