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A Highlights from MBoC Selection: Finding the Cell Center by a Balance of Dynein and Myosin Pulling and Microtubule Pushing: A Computational Study

机译:MBoC选择的一个亮点:通过动力蛋白和肌球蛋白的牵拉与微管推挤的平衡找到细胞中心:一项计算研究

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摘要

The centrosome position in many types of interphase cells is actively maintained in the cell center. Our previous work indicated that the centrosome is kept at the center by pulling force generated by dynein and actin flow produced by myosin contraction and that an unidentified factor that depends on microtubule dynamics destabilizes position of the centrosome. Here, we use modeling to simulate the centrosome positioning based on the idea that the balance of three forces—dyneins pulling along microtubule length, myosin-powered centripetal drag, and microtubules pushing on organelles—is responsible for the centrosome displacement. By comparing numerical predictions with centrosome behavior in wild-type and perturbed interphase cells, we rule out several plausible hypotheses about the nature of the microtubule-based force. We conclude that strong dynein- and weaker myosin-generated forces pull the microtubules inward competing with microtubule plus-ends pushing the microtubule aster outward and that the balance of these forces positions the centrosome at the cell center. The model also predicts that kinesin action could be another outward-pushing force. Simulations demonstrate that the force-balance centering mechanism is robust yet versatile. We use the experimental observations to reverse engineer the characteristic forces and centrosome mobility.
机译:在许多类型的相间细胞中,中心体位置被积极地维持在细胞中心。我们以前的工作表明,通过动力蛋白产生的拉力和肌球蛋白收缩产生的肌动蛋白流动,中心体被保持在中心,而依赖于微管动力学的不确定因素破坏了中心体的位置。在这里,我们使用建模来模拟中心体定位,其依据是三个力的平衡-动力蛋白沿微管长度拉动,肌球蛋白驱动的向心阻力和微管对细胞器的推动-是中心体移位的原因。通过将数值预测与野生型和扰动的相间细胞中的中心体行为进行比较,我们排除了有关基于微管力的性质的一些合理假设。我们得出的结论是,由动力蛋白产生的强力和较弱的肌球蛋白产生的力将微管向内拉,与微管的正向竞争将微管翠菊向外推,并且这些力的平衡将中心体定位在细胞中心。该模型还预测,驱动蛋白的作用可能是另一种向外推动力。仿真表明,力平衡定心机构既坚固又通用。我们使用实验观察来反向工程化特征力和中心体流动性。

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