Steffen Anika, Kage Frieda, Rottner Klemens
Department of Cell Biology, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Division of Molecular Cell Biology, Zoological Institute, Technische Universität Braunschweig, Braunschweig, Germany.
Methods Mol Biol. 2018;1749:257-277. doi: 10.1007/978-1-4939-7701-7_19.
Animal cell migration constitutes a complex process involving a multitude of forces generated and maintained by the actin cytoskeleton. Dynamic changes of the cell surface, for instance to effect cell edge protrusion, are at the core of initiating migratory processes, both in tissue culture models and whole animals. Here we sketch different aspects of imaging representative molecular constituents in such actin-driven processes, which power and regulate the polymerisation of actin filaments into bundles and networks, constituting the building blocks of such protrusions. The examples presented illustrate both the diversity of subcellular distributions of distinct molecular components, according to their function, and the complexity of dynamic changes in protrusion size, shape, and/or orientation in 3D. Considering these dynamics helps mechanistically connecting subcellular distributions of molecular machines driving protrusion and migration with their biochemical function.
动物细胞迁移是一个复杂的过程,涉及由肌动蛋白细胞骨架产生和维持的多种力。细胞表面的动态变化,例如导致细胞边缘突出,是在组织培养模型和整个动物中启动迁移过程的核心。在这里,我们概述了在这种由肌动蛋白驱动的过程中对代表性分子成分进行成像的不同方面,这些过程驱动并调节肌动蛋白丝聚合成束和网络,构成此类突出物的基本组成部分。所举的例子既说明了不同分子成分根据其功能在亚细胞分布上的多样性,也说明了三维空间中突出物大小、形状和/或方向动态变化的复杂性。考虑这些动态变化有助于从机制上将驱动突出和迁移的分子机器的亚细胞分布与其生化功能联系起来。