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Multiscale Modeling & Simulation最新文献

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From Signal Transduction to Spatial Pattern Formation in E. coli: A Paradigm for Multiscale Modeling in Biology 从大肠杆菌的信号转导到空间模式形成:生物学中多尺度建模的范例
IF 1.6 4区 数学 Q2 Physics and Astronomy Pub Date : 2005-01-01 DOI: 10.1137/040603565
R. Erban, H. Othmer
The collective behavior of bacterial populations provides an example of how cell-level decision making translates into population-level behavior and illustrates clearly the difficult multiscale mat...
细菌群体的集体行为提供了一个例子,说明细胞水平的决策如何转化为群体水平的行为,并清楚地说明了困难的多尺度问题。
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引用次数: 134
MULTISCALE TWO-DIMENSIONAL MODELING OF A MOTILE SIMPLE-SHAPED CELL. 运动单形细胞的多尺度二维建模。
IF 1.6 4区 数学 Q2 Physics and Astronomy Pub Date : 2005-01-01 DOI: 10.1137/04060370X
B Rubinstein, K Jacobson, A Mogilner

Cell crawling is an important biological phenomenon underlying coordinated cell movement in morphogenesis, cancer, and wound healing. In recent decades the process of cell crawling has been experimentally and theoretically dissected into further subprocesses: protrusion of the cell at its leading edge, retraction of the cell body, and graded adhesion. A number of one-dimensional (1-D) models explain successfully a proximal-distal organization and movement of the motile cell. However, more adequate two-dimensional (2-D) models are lacking. We propose a multiscale 2-D computational model of the lamellipodium (motile appendage) of a simply shaped, rapidly crawling fish keratocyte cell. We couple submodels of (i) protrusion and adhesion at the leading edge, (ii) the elastic 2-D lamellipodial actin network, (iii) the actin-myosin contractile bundle at the rear edge, and (iv) the convection-reaction-diffusion actin transport on the free boundary lamellipodial domain. We simulate the combined model numerically using a finite element approach. The simulations reproduce observed cell shapes, forces, and movements and explain some experimental results on perturbations of the actin machinery. This novel 2-D model of the crawling cell makes testable predictions and posits questions to be answered by future modeling.

细胞爬行是一种重要的生物学现象,是细胞在形态发生、癌症和伤口愈合过程中协调运动的基础。近几十年来,细胞爬行的过程在实验和理论上被进一步分解为几个子过程:细胞前缘的突出、细胞体的收缩和逐渐粘附。许多一维(1-D)模型成功地解释了运动细胞的近端到远端组织和运动。然而,缺乏更充分的二维(2-D)模型。我们提出了一个形状简单,快速爬行的鱼角质细胞的板状基底(运动附属物)的多尺度二维计算模型。我们耦合了(i)前缘的突出和粘附,(ii)弹性二维板形肌动蛋白网络,(iii)后边缘的肌动蛋白-肌球蛋白收缩束,以及(iv)自由边界板形结构域的对流-反应-扩散肌动蛋白运输的子模型。我们使用有限元方法对组合模型进行数值模拟。模拟重现了观察到的细胞形状、力和运动,并解释了肌动蛋白机制扰动的一些实验结果。这种新的爬行细胞的二维模型做出了可测试的预测,并提出了未来建模需要回答的问题。
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引用次数: 166
Homogenization method for transport of DNA particles in heterogeneous arrays 异质阵列中DNA颗粒运输的均质化方法
IF 1.6 4区 数学 Q2 Physics and Astronomy Pub Date : 2004-01-01 DOI: 10.1007/978-3-642-18756-8_2
A. Abdulle, S. Attinger
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引用次数: 10
Damping factors for the gap-tooth scheme 间隙齿形方案的阻尼因子
IF 1.6 4区 数学 Q2 Physics and Astronomy Pub Date : 2003-10-02 DOI: 10.1007/978-3-642-18756-8_6
G. Samaey, I. Kevrekidis, D. Roose
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引用次数: 19
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Multiscale Modeling & Simulation
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