Rubinstein Boris, Fournier Maxime F, Jacobson Ken, Verkhovsky Alexander B, Mogilner Alex
Stowers Institute for Medical Research, Kansas City, Missouri, USA.
Biophys J. 2009 Oct 7;97(7):1853-63. doi: 10.1016/j.bpj.2009.07.020.
The lamellipod, the locomotory region of migratory cells, is shaped by the balance of protrusion and contraction. The latter is the result of myosin-generated centripetal flow of the viscoelastic actin network. Recently, quantitative flow data was obtained, yet there is no detailed theory explaining the flow in a realistic geometry. We introduce models of viscoelastic actin mechanics and myosin transport and solve the model equations numerically for the flat, fan-shaped lamellipodial domain of keratocytes. The solutions demonstrate that in the rapidly crawling cell, myosin concentrates at the rear boundary and pulls the actin network inward, so the centripetal actin flow is very slow at the front, and faster at the rear and at the sides. The computed flow and respective traction forces compare well with the experimental data. We also calculate the graded protrusion at the cell boundary necessary to maintain the cell shape and make a number of other testable predictions. We discuss model implications for the cell shape, speed, and bi-stability.
片足是迁移细胞的运动区域,其形状由突出和收缩的平衡决定。后者是肌球蛋白产生的粘弹性肌动蛋白网络向心流的结果。最近,获得了定量流动数据,但尚无详细理论解释实际几何形状中的流动情况。我们引入了粘弹性肌动蛋白力学和肌球蛋白运输模型,并对角膜细胞的扁平扇形片足区域进行了模型方程的数值求解。结果表明,在快速爬行的细胞中,肌球蛋白集中在后边界并向内拉动肌动蛋白网络,因此向心肌动蛋白流在前端非常缓慢,在后端和两侧则较快。计算出的流动和相应的牵引力与实验数据吻合良好。我们还计算了维持细胞形状所需的细胞边界处的分级突出,并做出了一些其他可测试的预测。我们讨论了该模型对细胞形状、速度和双稳态的影响。