Department of Cell Biology, Duke University Medical Center, Durham, North Carolina, USA.
Biophys J. 2010 Nov 3;99(9):L78-80. doi: 10.1016/j.bpj.2010.09.024.
Recent work has indicated that the shape and size of a cell can influence how a cell spreads, develops focal adhesions, and exerts forces on the substrate. However, it is unclear how cell shape regulates these events. Here we present a computational model that uses cell shape to predict the magnitude and direction of forces generated by cells. The predicted results are compared to experimentally measured traction forces, and show that the model can predict traction force direction, relative magnitude, and force distribution within the cell using only cell shape as an input. Analysis of the model shows that the magnitude and direction of the traction force at a given point is proportional to the first moment of area about that point in the cell, suggesting that contractile forces within the cell act on the entire cytoskeletal network as a single cohesive unit. Through this model, we demonstrate that intrinsic properties of cell shape can facilitate changes in traction force patterns, independently of heterogeneous mechanical properties or signaling events within the cell.
最近的研究表明,细胞的形状和大小可以影响细胞的扩散方式、形成黏着斑以及对基质施加力的方式。然而,目前尚不清楚细胞形状如何调节这些事件。在这里,我们提出了一个计算模型,该模型使用细胞形状来预测细胞产生的力的大小和方向。预测结果与实验测量的牵引力进行了比较,结果表明,该模型仅使用细胞形状作为输入,就可以预测牵引力的方向、相对大小和细胞内的力分布。模型分析表明,在给定点处的牵引力的大小和方向与该点处细胞的第一矩面积成正比,这表明细胞内的收缩力作为一个整体的黏合单元作用于整个细胞骨架网络。通过该模型,我们证明了细胞形状的固有特性可以促进牵引力模式的变化,而与细胞内的异质性机械特性或信号事件无关。