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Modeling cell entry into a micro-channel

机译:模拟细胞进入微通道

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Cell entry into a micro-channel has potential applications in cell sorting and cancer diagnostics. In this paper, we numerically model breast cancer cell entry into a constricted micro-channel. Our results indicate that the cell velocity decreases during entry and increases after entry, an observation in agreement with experiments. We found that the cell entry time depend strongly on the cortical stiffness and is minimum at some critical cortical elasticity. In addition, we found that for the same entry time, a stiff nucleus is displaced toward the cell front, whereas a viscous nucleus is displaced toward the rear. In comparison, the nucleus is less sensitive to the viscosity of the cytoplasm. These observations suggest that specific intra-cellular properties can be deduced non-invasively during cell entry, through the inspection of the nucleus using suitable illumination techniques, such as fluorescent labeling.
机译:细胞进入微通道具有在细胞分选和癌症诊断中的潜在应用。在本文中,我们对乳腺癌细胞进入狭窄的微通道进行数值建模。我们的结果表明,细胞速度在进入过程中降低,而进入后则增加,这与实验一致。我们发现细胞进入时间在很大程度上取决于皮质的刚度,并且在某些临界皮质弹性上最小。另外,我们发现对于相同的进入时间,一个坚硬的核向着细胞的前部移动,而一个粘性的核向着细胞的后部移动。相比之下,细胞核对细胞质的粘度较不敏感。这些观察结果表明,可以通过使用合适的照明技术(例如荧光标记)检查细胞核,在细胞进入过程中无创地推导特定的细胞内特性。

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