Lange Julia, Bernitt Erik, Döbereiner Hans-Günther
Institute of Biophysics, University of Bremen, Bremen, Germany.
Front Cell Dev Biol. 2020 Jun 9;8:422. doi: 10.3389/fcell.2020.00422. eCollection 2020.
Lamellipodial and filopodial protrusions are two of the main aggregate types of filamentous actin in living cells. Even though filopodia are essential to a range of vital cell functions, the mechanisms leading to their formation are still debated. Filopodia are relatively stiff and rod-like structures that are embedded in the highly dynamic framework of the backward flowing meshwork of the lamellipodium. Phenomena such as lateral filopodia drift and collision events suggest that mechanical aspects play a significant role in filopodia dynamics. In this paper, we systematically analyze the interplay between the backward flow of actin in the lamellipodium and the drift velocity of actin bundles, that we identify to be filopodia, in a quantitative manner in cells of given morphology and controlled myosin activity. Moreover, we study mechanical aspects of fusion of actin bundles drifting laterally in the lamellipodium. We find that the dynamics of actin bundles drift and fusion can be captured in a mechanical framework, which leads to a model of actin bundles orientation.
片状伪足和丝状伪足突出是活细胞中丝状肌动蛋白的两种主要聚集类型。尽管丝状伪足对于一系列重要的细胞功能至关重要,但其形成机制仍存在争议。丝状伪足是相对坚硬的棒状结构,嵌入在片状伪足向后流动的网络的高度动态框架中。诸如侧向丝状伪足漂移和碰撞事件等现象表明,力学方面在丝状伪足动力学中起着重要作用。在本文中,我们系统地分析了在给定形态和受控肌球蛋白活性的细胞中,片状伪足中肌动蛋白的向后流动与我们确定为丝状伪足的肌动蛋白束的漂移速度之间的相互作用。此外,我们研究了在片状伪足中横向漂移的肌动蛋白束融合的力学方面。我们发现,肌动蛋白束漂移和融合的动力学可以在一个力学框架中得到描述,这导致了一个肌动蛋白束取向模型。