Dufort P A, Lumsden C J
Institute of Medical Science, University of Toronto, Canada.
Cell Motil Cytoskeleton. 1996;35(4):309-30. doi: 10.1002/(SICI)1097-0169(1996)35:4<309::AID-CM4>3.0.CO;2-1.
The role of ATP hydrolysis in the regulation of the actin cytoskeleton continues to be a subject of controversy. Since actin polymerization can occur in the absence of ATP, the energy of hydrolysis is not needed for filament assembly. Recent work has instead suggested a regulatory role for ATP in cytoskeletal remodeling. In particular, both profilin and free filament barbed ends have been shown to play major roles in the processing of ATP by actin. We have developed a new integrated kinetic model to examine how the maintenance of the pool of unpolymerized actin and the flux of actin subunits through filaments are controlled by profilin and free filament barbed ends through their interaction with ATP. An analysis of the model's steady states predicts how two novel regulatory pathways may regulate the cytoskeleton in vivo. Coordinated changes in the availability of both profilin and free barbed ends mediate the following regulatory effects: (1) both the nucleotide composition and the absolute amount of free G-actin can be changed separately or together to substantially alter the total amount of F-actin; and (2) uncapping the barbed ends of only a modest fraction of filaments causes all filaments to begin slowly depolymerizing from their pointed ends, resulting in the total depolymerization of the remaining capped filaments. We report that the phenomenon of treadmilling, wherein the barbed end growth of each filament is exactly balanced by pointed end loss at steady state, is only possible in the limiting case when all barbed ends are uncapped. The capping of any fraction of barbed ends increases the critical concentration of ATP-G-actin, causing the remaining free barbed ends to grow faster than their pointed ends can shrink. On the basis of these findings we propose a major revision to the treadmilling model for actin-based motility, in which the rapidly growing filaments with free barbed ends are continuously severed toward their rear followed by capping of the newly exposed barbed ends. This revised model, herein referred to as "treadsevering," allows sustained and rapid barbed end growth to occur indefinitely at a steady state provided a continuous input of ATP.
ATP水解在肌动蛋白细胞骨架调节中的作用一直是一个有争议的话题。由于肌动蛋白聚合可以在没有ATP的情况下发生,水解能量对于丝状体组装并非必需。最近的研究反而表明ATP在细胞骨架重塑中具有调节作用。特别是,已证明肌动蛋白结合蛋白和游离丝状体的带刺末端在肌动蛋白对ATP的处理中起主要作用。我们开发了一种新的综合动力学模型,以研究未聚合肌动蛋白库的维持以及肌动蛋白亚基通过细丝的通量如何通过肌动蛋白结合蛋白和游离细丝带刺末端与ATP的相互作用来控制。对模型稳态的分析预测了两种新的调节途径如何在体内调节细胞骨架。肌动蛋白结合蛋白和游离带刺末端可用性的协调变化介导以下调节作用:(1)游离G-肌动蛋白的核苷酸组成和绝对量可以分别或一起改变,从而大幅改变F-肌动蛋白的总量;(2)仅解开一小部分细丝的带刺末端会导致所有细丝从其尖端开始缓慢解聚,导致其余带帽细丝完全解聚。我们报告说,踏车运动现象,即在稳态下每个细丝的带刺末端生长与尖端损失精确平衡,只有在所有带刺末端都未加帽的极限情况下才可能发生。任何比例的带刺末端加帽都会增加ATP-G-肌动蛋白的临界浓度,导致其余游离带刺末端的生长速度超过其尖端的收缩速度。基于这些发现,我们对基于肌动蛋白的运动的踏车运动模型提出了重大修订,其中具有游离带刺末端的快速生长细丝在其后部不断被切断,随后新暴露的带刺末端被加帽。这种修订后的模型,在此称为“踏切”,只要有持续的ATP输入,就可以在稳态下无限期地持续快速的带刺末端生长。