Cytrynbaum E N, Rodionov V, Mogilner A
Laboratory of Cell and Computational Biology, Department of Mathematics and Center for Genetics and Development, University of California, Davis, CA 95616, USA.
J Cell Sci. 2004 Mar 15;117(Pt 8):1381-97. doi: 10.1242/jcs.00919. Epub 2004 Mar 2.
Polar arrays of microtubules play many important roles in the cell. Normally, such arrays are organized by a centrosome anchoring the minus ends of the microtubules, while the plus ends extend to the cell periphery. However, ensembles of molecular motors and microtubules also demonstrate the ability to self-organize into polar arrays. We use quantitative modeling to analyze the self-organization of microtubule asters and the aggregation of motor-driven pigment granules in fragments of fish melanophore cells. The model is based on the observation that microtubules are immobile and treadmilling, and on the experimental evidence that cytoplasmic dynein motors associated with granules have the ability to nucleate MTs and attenuate their minus-end dynamics. The model explains the observed sequence of events as follows. Initially, pigment granules driven by cytoplasmic dynein motors aggregate to local clusters of microtubule minus ends. The pigment aggregates then nucleate microtubules with plus ends growing toward the fragment boundary, while the minus ends stay transiently in the aggregates. Microtubules emerging from one aggregate compete with any aggregates they encounter leading to the gradual formation of a single aggregate. Simultaneously, a positive feedback mechanism drives the formation of a single MT aster--a single loose aggregate leads to focused MT nucleation and hence a tighter aggregate which stabilizes MT minus ends more effectively leading to aster formation. We translate the model assumptions based on experimental measurements into mathematical equations. The model analysis and computer simulations successfully reproduce the observed pathways of pigment aggregation and microtubule aster self-organization. We test the model predictions by observing the self-organization in fragments of various sizes and in bi-lobed fragments. The model provides stringent constraints on rates and concentrations describing microtubule and motor dynamics, and sheds light on the role of polymer dynamics and polymer-motor interactions in cytoskeletal organization.
微管的极性阵列在细胞中发挥着许多重要作用。通常情况下,此类阵列由锚定微管负端的中心体组织而成,而正端则延伸至细胞周边。然而,分子马达和微管的集合也展现出自我组织成极性阵列的能力。我们运用定量建模来分析微管星状体的自我组织以及鱼类黑素细胞片段中马达驱动色素颗粒的聚集情况。该模型基于微管静止和踏车运动的观察结果,以及与颗粒相关的胞质动力蛋白马达能够使微管成核并减弱其负端动力学的实验证据。该模型对观察到的事件序列解释如下。最初,由胞质动力蛋白马达驱动的色素颗粒聚集到微管负端的局部簇中。然后,色素聚集体使微管成核,其正端朝着片段边界生长,而负端则暂时留在聚集体中。从一个聚集体中出现的微管会与它们遇到的任何聚集体竞争,导致逐渐形成单个聚集体。同时,一种正反馈机制驱动单个微管星状体的形成——单个松散聚集体导致集中的微管成核,进而形成更紧密的聚集体,更有效地稳定微管负端,从而导致星状体形成。我们将基于实验测量的模型假设转化为数学方程。模型分析和计算机模拟成功地重现了观察到的色素聚集和微管星状体自我组织的途径。我们通过观察各种大小的片段以及双叶片段中的自我组织来检验模型预测。该模型对描述微管和马达动力学的速率和浓度提供了严格的限制,并揭示了聚合物动力学和聚合物 - 马达相互作用在细胞骨架组织中的作用。