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Sub-micron lateral topography affects endothelial migration by modulation of focal adhesion dynamics

机译:亚微米侧面形貌通过调节粘着动力学来影响内皮迁移

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Through the interaction with topographical features, endothelial cells tune their ability to populate target substrates, both in vivo and in vitro. Basal textures interfere with the establishment and maturation of focal adhesions (FAs) thus inducing specific cell-polarization patterns and regulating a plethora of cell activities that govern the overall endothelial function. In this study, we analyze the effect of topographical features on FAs in primary human endothelial cells. Reported data demonstrate a functional link between FA dynamics and cell polarization and spreading on structured substrates presenting variable lateral feature size. Our results reveal that gratings with 2 mu m lateral periodicity maximize contact guidance. The effect is linked to the dynamical state of FAs. We argue that these results are readily applicable to the rational design of active surfaces at the interface with the blood stream.
机译:通过与地形特征的相互作用,内皮细胞在体内和体外均可调节其填充靶标底物的能力。基底纹理干扰粘着斑(FAs)的建立和成熟,从而诱导特定的细胞极化模式并调节控制整个内皮功能的过多细胞活动。在这项研究中,我们分析了地形特征对原代人内皮细胞FAs的影响。报道的数据证明了FA动力学与细胞极化之间的功能联系,并在结构化基底上扩散,呈现出可变的横向特征尺寸。我们的结果表明,横向周期性为2μm的光栅可以最大化接触引导。该影响与FA的动态状态有关。我们认为这些结果很容易适用于与血流界面处的活性表面的合理设计。

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