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Characterization of the cellular biomechanical responses caused on microprocessed substrates: effect of micropatterned cell adhesiveness and microelasticity gradient

机译:微处理基材引起的细胞生物力学响应的表征:微透滞细胞粘附性和微弹性梯度的影响

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摘要

To investigate the shape-dependent cell mechanics and ECM-dependent control of motility, cell elasticity, structural features of the actin cytoskeleton (CSK) and motility responses were characterized on well-designed microprocessed substrates with micropatterned cell adhesive regions and microelastic gradient. Cell elasticity and actin CSK features of shape-engineered fibroblasts and vascular endothelial cells (round and spindle-shaped) cultured on photolithographically microprocessed surfaces were characterized employing the cellular microindentation test and fluorescence observation of actin CSK by the combination of atomic force microscopy (AFM) and fluorescence microscopy (FM). Condition of directional cell movement towards stiffer region, so called mechanotaxis, was studied on the photolithographically-microprocessed microelastic gradient gel (MEG gel). The interrelationships between cell elasticity, the structural features of actin CSK and engineered cell shape were analyzed as compared with control cells cultured on non-processed surfaces (termed naturally extended cells). The results showed that the elasticity of regionally restricted adhesion-surface-induced shape-engineered cells, particularly highly elongated cells, is predominantly affected by cell shape rather than by the structural features of SFs. As for the mechanotaxis behaviors induced on MEG gel, design of both elasticity jump and discreteness in the elasticity boundary was found to be essential to cause cellular directional movement.
机译:为了研究形状依赖的细胞力学和依赖于运动性,电池弹性,肌动蛋白细胞骨架(CSK)的结构特征和运动反应的结构特征,其特征在于设计良好设计的微处理底物和微弹性梯度。在光刻微处理表面上培养的形状工程成纤维细胞和血管内皮细胞(圆形和轴形)的细胞弹性和肌动蛋白CSK特征的特征在于采用原子力显微镜(AFM)的组合采用肌动蛋白CSK的细胞微观调节试验和荧光观察和荧光显微镜(FM)。研究了光刻微塑性梯度凝胶(MEG凝胶)研究了朝向更硬区域的定向细胞运动的条件。与在非加工表面上培养的对照细胞(称为天然延长的细胞)的对照细胞相比,分析了细胞弹性之间的相互关系,肌动蛋白CSK和工程细胞形状的结构特征。结果表明,区域限制粘合表面诱导的形状工程化细胞,特别是高细长细胞的弹性主要受细胞形状的影响,而不是通过SFS的结构特征影响。关于在MEG凝胶上诱导的机制行为,发现弹性边界的弹性跳跃和离散性的设计是必要的,以引起蜂窝定向运动。

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