Heyn Johannes C J, Rädler Joachim O, Falcke Martin
Fakultät für Physik, Ludwig-Maximilians-Universität München (LMU), Munich, Germany.
Max Delbrück Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany.
Front Cell Dev Biol. 2024 Apr 16;12:1352279. doi: 10.3389/fcell.2024.1352279. eCollection 2024.
Quantitative studies of mesenchymal cell motion are important to elucidate cytoskeleton function and mechanisms of cell migration. To this end, confinement of cell motion to one dimension (1D) significantly simplifies the problem of cell shape in experimental and theoretical investigations. Here we review 1D migration assays employing micro-fabricated lanes and reflect on the advantages of such platforms. Data are analyzed using biophysical models of cell migration that reproduce the rich scenario of morphodynamic behavior found in 1D. We describe basic model assumptions and model behavior. It appears that mechanical models explain the occurrence of universal relations conserved across different cell lines such as the adhesion-velocity relation and the universal correlation between speed and persistence (UCSP). We highlight the unique opportunity of reproducible and standardized 1D assays to validate theory based on statistical measures from large data of trajectories and discuss the potential of experimental settings embedding controlled perturbations to probe response in migratory behavior.
间充质细胞运动的定量研究对于阐明细胞骨架功能和细胞迁移机制至关重要。为此,将细胞运动限制在一维(1D)在实验和理论研究中能显著简化细胞形状问题。在此,我们回顾采用微加工通道的一维迁移测定法,并思考此类平台的优势。使用细胞迁移的生物物理模型分析数据,该模型再现了一维中发现的丰富形态动力学行为场景。我们描述了基本模型假设和模型行为。似乎力学模型解释了不同细胞系中守恒的普遍关系的出现,如粘附 - 速度关系以及速度与持续性之间的普遍相关性(UCSP)。我们强调了可重复和标准化的一维测定法基于轨迹大数据的统计测量来验证理论的独特机会,并讨论了嵌入受控扰动的实验设置在探究迁移行为响应方面的潜力。