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The Kinetics of Force-Induced Cell Reorganization Depend on Microtubules and Actin

机译:力诱导细胞重组的动力学取决于微管和肌动蛋白。

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摘要

The cytoskeleton is an important factor in the functional and structural adaption of cells to mechanical forces. In this study we investigated the impact of microtubules and the acto-myosin machinery on the kinetics of force-induced reorientation of NIH3T3 fibroblasts. These cells were subjected to uniaxial stretching forces that are known to induce cellular reorientation perpendicular to the stretch direction. We found that disruption of filamentous actin using cytochalasin D and latrunculin B as well as an induction of a massive unpolarized actin polymerization by jasplakinolide, inhibited the stretch-induced reorientation. Similarly, blocking of myosin II activity abolished the stretch-induced reorientation of cells but, interestingly, increased their motility under stretching conditions in comparison to myosin-inhibited nonstretched cells. Investigating the contribution of microtubules to the cellular reorientation, we found that, although not playing a significant role in reorientation itself, microtubule stability had a significant impact on the kinetics of this event. Overall, we conclude that acto-myosin, together with microtubules, regulate the kinetics of force-induced cell reorientation. © 2010 Wiley-Liss, Inc.
机译:细胞骨架是细胞对机械力的功能和结构适应的重要因素。在这项研究中,我们研究了微管和肌球蛋白肌动蛋白机制对力诱导的NIH3T3成纤维细胞重新定向动力学的影响。这些细胞经受单轴拉伸力,已知该单轴拉伸力会诱导垂直于拉伸方向的细胞重新定向。我们发现,使用细胞松弛素D和latrunculin B破坏丝状肌动蛋白,以及通过Jasplakinolide诱导大规模的非极化肌动蛋白聚合,抑制了拉伸诱导的重新定向。同样,肌球蛋白II活性的阻断消除了拉伸诱导的细胞重新定向,但有趣的是,与肌球蛋白抑制的未拉伸细胞相比,在拉伸条件下增加了它们的运动能力。调查微管对细胞重新定向的贡献,我们发现,尽管微管本身在重新定向中没有发挥重要作用,但微管稳定性对这一事件的动力学有重大影响。总的来说,我们得出结论,肌动球蛋白与微管一起调节力诱导细胞重新定向的动力学。 ©2010 Wiley-Liss,Inc.

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