Zadeh Pedrom, Camley Brian A
William H. Miller III Department of Physics & Astronomy, Johns Hopkins University, Baltimore, Maryland 21205, USA.
William H. Miller III Department of Physics & Astronomy and Thomas C. Jenkins Department of Biophysics, Johns Hopkins University, Baltimore, Maryland 21205, USA.
PRX Life. 2024 Oct-Dec;2(4). doi: 10.1103/prxlife.2.043020. Epub 2024 Dec 20.
The motility of eukaryotic cells is strongly influenced by their environment, with confined cells often developing qualitatively different motility patterns from those migrating on simple two-dimensional substrates. Recent experiments, coupled with data-driven methods to extract a cell's equation of motion, showed that cancerous MDA-MB-231 cells persistently hop in a limit cycle when placed on two-state adhesive micropatterns (two large squares connected by a narrow bridge), while they remain stationary on average in rectangular confinements. In contrast, healthy MCF10A cells migrating on the two-state micropattern are bistable, i.e., they settle into either basin on average with only noise-induced hops between the two states. We can capture all these behaviors with a single computational phase field model of a crawling cell, under the assumption that contact with nonadhesive substrate inhibits the cell front. Our model predicts that larger and softer cells are more likely to persistently hop, while smaller and stiffer cells are more likely to be bistable. Other key factors controlling cell migration are the frequency of protrusions and their magnitude of noise. Our results show that relatively simple assumptions about how cells sense their geometry can explain a wide variety of different cell behaviors, and show the power of data-driven approaches to characterize both experiment and simulation.
真核细胞的运动性受到其环境的强烈影响,与在简单二维基质上迁移的细胞相比,受限细胞通常会形成性质不同的运动模式。最近的实验,结合数据驱动方法来提取细胞的运动方程,结果表明,癌性MDA-MB-231细胞放置在双态粘性微图案(由狭窄桥连接的两个大正方形)上时会在极限环中持续跳跃,而在矩形限制条件下它们平均保持静止。相比之下,在双态微图案上迁移的健康MCF10A细胞具有双稳态,即它们平均会进入其中一个状态,只有在两个状态之间由噪声引起的跳跃。在与非粘性底物接触会抑制细胞前端的假设下,我们可以用一个爬行细胞的计算相场模型来捕捉所有这些行为。我们的模型预测,更大、更软的细胞更有可能持续跳跃,而更小、更硬的细胞更有可能处于双稳态。控制细胞迁移的其他关键因素是突起的频率及其噪声幅度。我们的结果表明,关于细胞如何感知其几何形状的相对简单假设可以解释各种各样不同的细胞行为,并展示了数据驱动方法在表征实验和模拟方面的强大作用。