Keren Kinneret, Yam Patricia T, Kinkhabwala Anika, Mogilner Alex, Theriot Julie A
Department of Biochemistry and Howard Hughes Medical Institute, Stanford University School of Medicine, Stanford, California 94305, USA.
Nat Cell Biol. 2009 Oct;11(10):1219-24. doi: 10.1038/ncb1965. Epub 2009 Sep 20.
Cytosolic fluid dynamics have been implicated in cell motility because of the hydrodynamic forces they induce and because of their influence on transport of components of the actin machinery to the leading edge. To investigate the existence and the direction of fluid flow in rapidly moving cells, we introduced inert quantum dots into the lamellipodia of fish epithelial keratocytes and analysed their distribution and motion. Our results indicate that fluid flow is directed from the cell body towards the leading edge in the cell frame of reference, at about 40% of cell speed. We propose that this forward-directed flow is driven by increased hydrostatic pressure generated at the rear of the cell by myosin contraction, and show that inhibition of myosin II activity by blebbistatin reverses the direction of fluid flow and leads to a decrease in keratocyte speed. We present a physical model for fluid pressure and flow in moving cells that quantitatively accounts for our experimental data.
由于胞质流体动力学所诱导的流体动力以及它们对肌动蛋白机制成分向细胞前沿运输的影响,其已被认为与细胞运动有关。为了研究快速移动细胞中流体流动的存在及其方向,我们将惰性量子点引入鱼类上皮角质形成细胞的片状伪足中,并分析它们的分布和运动。我们的结果表明,在细胞参考系中,流体流动是从细胞体指向细胞前沿的,速度约为细胞速度的40%。我们提出,这种向前的流动是由肌球蛋白收缩在细胞后部产生的静水压力增加所驱动的,并表明blebbistatin对肌球蛋白II活性的抑制会使流体流动方向逆转,并导致角质形成细胞速度降低。我们提出了一个移动细胞中流体压力和流动的物理模型,该模型定量地解释了我们的实验数据。