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Cell Adhesion Dynamics and Actin Cytoskeleton Reorganization in HepG2 Cell Aggregates

机译:HepG2细胞聚集体中的细胞粘附动力学和肌动蛋白细胞骨架重组。

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The temporal dependence of cytoskeletal remodelling on cell-cell contact in HepG2 cells has been established here. Cell-cell contact occurred in an ultrasound standing wave trap designed to form and levitate a 2-D cell aggregate, allowing intercellular adhesive interactions to proceed, free from the influences of solid substrata. Membrane spreading at the point of contact and change in cell circularity reached 50% of their final values within 2.2 min of contact. Junctional F-actin increased at the interface but lagged behind membrane spreading, reaching 50% of its final value in 4.4 min. Aggregates had good mechanical stability after 15 min in the trap. The implication of this temporal dependence on the sequential progress of adhesion processes is discussed. These results provide insight into how biomimetic cell aggregates with some liver cell functions might be assembled in a systematic, controlled manner in a 3-D ultrasound trap.
机译:在这里已经建立了HepG2细胞中细胞骨架重塑对细胞接触的时间依赖性。细胞与细胞之间的接触发生在超声波驻波阱中,该阱设计用于形成和悬浮二维细胞聚集体,从而使细胞间的粘附相互作用得以进行,而不受固体基质的影响。在接触点2.2分钟内,膜在接触点处铺展和细胞圆形度变化达到其最终值的50%。接合F-肌动蛋白在界面处增加,但滞后于膜铺展,在4.4分钟内达到其最终值的50%。收集器中的集料在15分钟后具有良好的机械稳定性。讨论了这种时间依赖性对粘附过程顺序进展的影响。这些结果提供了洞悉如何将具有某些肝细胞功能的仿生细胞聚集体以系统,可控的方式组装在3-D超声阱中的方法。

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