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单细胞在短微槽上的准周期迁移。

Quasi-periodic migration of single cells on short microlanes.

机构信息

Faculty of Physics and Center for NanoScience, Ludwig-Maximilians-Universität München, Munich, Germany.

Arnold-Sommerfeld-Center for Theoretical Physics, Faculty of Physics and Center for NanoScience, Ludwig-Maximilians-Universität München, Munich, Germany.

出版信息

PLoS One. 2020 Apr 13;15(4):e0230679. doi: 10.1371/journal.pone.0230679. eCollection 2020.

DOI:10.1371/journal.pone.0230679
PMID:32282802
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7153896/
Abstract

Cell migration on microlanes represents a suitable and simple platform for the exploration of the molecular mechanisms underlying cell cytoskeleton dynamics. Here, we report on the quasi-periodic movement of cells confined in stripe-shaped microlanes. We observe persistent polarized cell shapes and directed pole-to-pole motion within the microlanes. Cells depolarize at one end of a given microlane, followed by delayed repolarization towards the opposite end. We analyze cell motility via the spatial velocity distribution, the velocity frequency spectrum and the reversal time as a measure for depolarization and spontaneous repolarization of cells at the microlane ends. The frequent encounters of a boundary in the stripe geometry provides a robust framework for quantitative investigations of the cytoskeleton protrusion and repolarization dynamics. In a first advance to rigorously test physical models of cell migration, we find that the statistics of the cell migration is recapitulated by a Cellular Potts model with a minimal description of cytoskeleton dynamics. Using LifeAct-GFP transfected cells and microlanes with differently shaped ends, we show that the local deformation of the leading cell edge in response to the tip geometry can locally either amplify or quench actin polymerization, while leaving the average reversal times unaffected.

摘要

细胞在微槽上的迁移代表了一种用于探索细胞骨架动力学的分子机制的合适而简单的平台。在这里,我们报告了细胞在条状微槽中的准周期运动。我们观察到细胞在微槽内保持持久的极化形状和定向的极到极运动。细胞在给定微槽的一端去极化,然后延迟向相反端复极化。我们通过空间速度分布、速度频谱和反转时间来分析细胞的迁移运动,以反转时间作为细胞在微槽两端去极化和自发复极化的度量。条纹几何形状中的边界频繁相遇为细胞骨架突起和复极化动力学的定量研究提供了一个稳健的框架。作为严格检验细胞迁移物理模型的第一个进展,我们发现细胞迁移的统计数据可以通过具有最小细胞骨架动力学描述的细胞势模型来再现。使用 LifeAct-GFP 转染的细胞和具有不同形状末端的微槽,我们表明,在响应尖端几何形状时,前导细胞边缘的局部变形可以局部地放大或抑制肌动蛋白聚合,而平均反转时间不受影响。

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Ring-Shaped Microlanes and Chemical Barriers as a Platform for Probing Single-Cell Migration.环形微沟道和化学障碍作为探测单细胞迁移的平台。
Sci Rep. 2016 May 31;6:26858. doi: 10.1038/srep26858.
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