Department of Basic Science, Graduate School of Arts and Sciences, University of Tokyo, Meguro-ku 153-8902, Japan.
Universal Biological Institute, University of Tokyo, Bunkyo-ku 113-0033, Japan.
Proc Natl Acad Sci U S A. 2021 Dec 14;118(50). doi: 10.1073/pnas.2110281118.
In fast-moving cells such as amoeba and immune cells, dendritic actin filaments are spatiotemporally regulated to shape large-scale plasma membrane protrusions. Despite their importance in migration, as well as in particle and liquid ingestion, how their dynamics are affected by micrometer-scale features of the contact surface is still poorly understood. Here, through quantitative image analysis of on microfabricated surfaces, we show that there is a distinct mode of topographical guidance directed by the macropinocytic membrane cup. Unlike other topographical guidance known to date that depends on nanometer-scale curvature sensing protein or stress fibers, the macropinocytic membrane cup is driven by the Ras/PI3K/F-actin signaling patch and its dependency on the micrometer-scale topographical features, namely PI3K/F-actin-independent accumulation of Ras-GTP at the convex curved surface, PI3K-dependent patch propagation along the convex edge, and its actomyosin-dependent constriction at the concave edge. Mathematical model simulations demonstrate that the topographically dependent initiation, in combination with the mutually defining patch patterning and the membrane deformation, gives rise to the topographical guidance. Our results suggest that the macropinocytic cup is a self-enclosing structure that can support liquid ingestion by default; however, in the presence of structured surfaces, it is directed to faithfully trace bent and bifurcating ridges for particle ingestion and cell guidance.
在变形虫和免疫细胞等快速运动的细胞中,树突状肌动蛋白丝在时空上受到调节,以形成大规模的质膜突起。尽管它们在迁移以及颗粒和液体摄取中很重要,但它们的动力学如何受到接触表面微米级特征的影响仍知之甚少。在这里,我们通过对微加工表面上的进行定量图像分析,表明存在一种由大吞噬质膜杯引导的明显的形貌导向模式。与迄今为止已知的依赖于纳米级曲率感应蛋白或应力纤维的其他形貌导向不同,大吞噬质膜杯由 Ras/PI3K/F-actin 信号斑驱动,并且依赖于微米级形貌特征,即 Ras-GTP 在凸面的 PI3K/F-actin 非依赖性积累、PI3K 依赖性斑块沿着凸缘的传播以及在凹缘处的肌动球蛋白依赖性收缩。数学模型模拟表明,形貌依赖性的启动,结合斑块模式的相互定义和膜变形,导致了形貌导向。我们的结果表明,大吞噬杯是一种自封闭的结构,默认情况下可以支持液体摄取;然而,在存在结构化表面的情况下,它会被引导去忠实地跟踪弯曲和分叉的脊,以进行颗粒摄取和细胞导向。