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由细丝蛋白交联的肌动蛋白丝网络的弹性特性和变形机制。

The elastic properties and deformation mechanisms of actin filament networks crosslinked by filamins.

作者信息

Wang Xiaobo, Zhu Hanxing, Lu Yongtao, Wang Zuobin, Kennedy David

机构信息

School of Engineering, Cardiff University, Cardiff, CF24 3AA, UK.

School of Engineering, Cardiff University, Cardiff, CF24 3AA, UK.

出版信息

J Mech Behav Biomed Mater. 2020 Dec;112:104075. doi: 10.1016/j.jmbbm.2020.104075. Epub 2020 Sep 6.

DOI:10.1016/j.jmbbm.2020.104075
PMID:32942229
Abstract

As a substructure of cell cytoskeleton, the crosslinked actin filament networks (CAFNs) play a major role in different cell functions, however, the elastic properties and the deformation mechanisms of CAFNs still remain to be understood. In this paper, a novel three-dimensional (3D) finite element (FE) model has been developed to mimic the mechanical properties of actin filament (F-actin) networks crosslinked by filamin A (FLNA). The simulation results indicate that although the Young's modulus of CAFNs varies in different directions for each random model, the statistical mean value is in-plane isotropic. The crosslinking density and the actin filament volume fraction are found to strongly affect the in-plane shear modulus of CAFNs. The simulation results agree well with the relevant experimental results. In addition, an L-shaped cantilever beam model has been developed for dimensional analysis on the shear stiffness of CAFNs and for quantifying the deformation mechanisms. It has been demonstrated that the in-plane shear modulus of CAFNs is mainly dominated by FLNA (i.e., cross-linkers), and that the bending and torsion deformations of FLNA have almost the same contribution to the stiffness of CAFNs. It has also been found that the stiffness of CAFNs is almost insensitive to the variation of the Poisson's ratios of FLNA and actin filament in the range from 0.29 to 0.499.

摘要

作为细胞骨架的一个子结构,交联肌动蛋白丝网络(CAFNs)在不同的细胞功能中发挥着重要作用,然而,CAFNs的弹性特性和变形机制仍有待了解。本文建立了一种新颖的三维(3D)有限元(FE)模型,以模拟由细丝蛋白A(FLNA)交联的肌动蛋白丝(F-肌动蛋白)网络的力学性能。模拟结果表明,尽管每个随机模型的CAFNs杨氏模量在不同方向上有所不同,但其统计平均值在面内是各向同性的。发现交联密度和肌动蛋白丝体积分数对CAFNs的面内剪切模量有强烈影响。模拟结果与相关实验结果吻合良好。此外,还建立了一个L形悬臂梁模型,用于对CAFNs的剪切刚度进行尺寸分析和量化变形机制。结果表明,CAFNs的面内剪切模量主要由FLNA(即交联剂)决定,并且FLNA的弯曲和扭转变形对CAFNs的刚度贡献几乎相同。还发现,在0.29至0.499的范围内,CAFNs的刚度对FLNA和肌动蛋白丝泊松比的变化几乎不敏感。

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