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Investigating Circular Dorsal Ruffles through Varying Substrate Stiffness and Mathematical Modeling

机译:通过改变基底刚度和数学建模研究圆形背褶

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摘要

Circular dorsal ruffles (CDRs) are transient actin-rich ringlike structures that form on the dorsal surface of growth-factor stimulated cells. However, the dynamics and mechanism of formation of CDRs are still unknown. It has been observed that CDR formation leads to stress fibers disappearing near the CDRs. Because stress fiber formation can be modified by substrate stiffness, we examined the effect of substrate stiffness on CDR formation by seeding NIH 3T3 fibroblasts on glass and polydimethylsiloxane substrates of varying stiffnesses from 20 kPa to 1800 kPa. We found that increasing substrate stiffness increased the lifetime of the CDRs. We developed a mathematical model of the signaling pathways involved in CDR formation to provide insight into this lifetime and size dependence that is linked to substrate stiffness via Rac-Rho antagonism. From the model, increasing stiffness raised mDia1-nucleated stress fiber formation due to Rho activation. The increased stress fibers present increased replenishment of the G-actin pool, therefore prolonging Arp2/3-nucleated CDR formation due to Rac activation. Negative feedback by WAVE-related RacGAP on Rac explained how CDR actin propagates as an excitable wave, much like wave propagation in other excitable medium, e.g., nerve signal transmission.
机译:环状背褶(CDR)是在生长因子刺激的细胞的背面形成的富含肌动蛋白的瞬时环状结构。但是,CDR的动力学和形成机理仍然未知。已经观察到,CDR的形成导致应力纤维在CDR附近消失。因为应力纤维的形成可以通过基底刚度来改变,所以我们通过在20kPa至1800kPa刚度之间变化的玻璃和聚二甲基硅氧烷基底上播种NIH 3T3成纤维细胞来检查基底刚度对CDR形成的影响。我们发现增加底物刚度可以增加CDR的寿命。我们开发了涉及CDR形成的信号通路的数学模型,以提供对这一寿命和大小依赖性的了解,该依赖性和大小依赖性通过Rac-Rho拮抗作用与底物刚度相关。从模型中,由于Rho激活,增加刚度会增加mDia1形核应力纤维的形成。应力纤维的增加表示G-肌动蛋白池的补充增加,因此由于Rac激活而延长了Arp2 / 3-有核CDR的形成。 WAVE相关RacGAP对Rac的负反馈解释了CDR肌动蛋白如何作为可兴奋波传播,就像波在其他可兴奋介质中的传播一样,例如神经信号传输。

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