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Intracellular forces during guided cell growth on micropatterns using FRET measurement

机译:使用FRET测量在微模式下引导细胞生长期间的细胞内力

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摘要

Interaction of cells with extracellular matrix (ECM) regulates cell shape, differentiation and polarity. This effect has been widely observed in cells grown on substrates with various patterned features, stiffness and surface chemistry. It has been postulated that mechanical confinement of cells by the substrate causes a redistribution of tension in cytoskeletal proteins resulting in cytoskeletal reorganization through force sensitive pathways. However, the mechanisms for force transduction during reorganization remain unclear. In this study, using FRET based force sensors we have measured tension in an actin cross-linking protein, α-actinin, and followed reorganization of actin cytoskeleton in real time in HEK cells grown on patterned substrates. We show that the patterned substrates cause a redistribution of tension in α-actinin that coincides with cytoskeleton reorganization. Higher tension was observed in portions of cells where they form bridges across inhibited regions of the patterned substrates; the attachment to the substrate is found to release tension. Real time measurements of α-actinin tension and F-actin arrangement show that an increase in tension coincides with formation of F-actin bundles at the cell periphery during cell-spreading across inhibited regions, suggesting that mechanical forces stimulate cytoskeleton enhancement. Rho-ROCK inhibitor (Y27632) causes reduction in actinin tension followed by retraction of bridged regions. Our results demonstrate that changes in cell shape and expansion over patterned surfaces is a force sensitive process that requires actomyosin contractile force involving Rho-ROCK pathway.
机译:细胞与细胞外基质(ECM)的相互作用调节细胞的形状,分化和极性。在具有各种图案特征,刚度和表面化学性质的底物上生长的细胞中,已广泛观察到这种效应。据推测,通过底物对细胞进行机械限制会导致细胞骨架蛋白中张力的重新分布,从而通过力敏感途径导致细胞骨架重组。但是,重组过程中的力传递机制仍然不清楚。在这项研究中,使用基于FRET的力传感器,我们测量了肌动蛋白交联蛋白α-actinin的张力,并实时观察了在图案化基质上生长的HEK细胞中肌动蛋白细胞骨架的重组情况。我们显示,图案化的底物会导致α-辅肌动蛋白张力的重新分布,这与细胞骨架重组相吻合。在细胞部分中观察到较高的张力,在这些部分中,它们在构图的底物的受抑制区域上形成了桥;发现与基材的附着会释放张力。 α-肌动蛋白张力和F-肌动蛋白排列的实时测量结果表明,张力的增加与跨抑制区域的细胞扩散过程中细胞外围F-肌动蛋白束的形成相吻合,表明机械力刺激了细胞骨架的增强。 Rho-ROCK抑制剂(Y27632)导致肌动蛋白张力降低,随后缩回桥接区域。我们的结果表明,细胞形状的变化和在图案化表面上的扩展是一个力敏感过程,需要肌动球蛋白收缩力涉及Rho-ROCK途径。

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