活细胞缩放律流变学中局部应力松弛的特征频率。

IF 3.2 3区 生物学 Q2 BIOPHYSICS Biophysical journal Pub Date : 2024-11-18 DOI:10.1016/j.bpj.2024.11.015
Jiu-Tao Hang, Huajian Gao, Guang-Kui Xu
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引用次数: 0

摘要

众所周知,活细胞在频谱上表现出幂律粘弹性响应和局部应力松弛行为。然而,分子尺度的细胞骨架动力学与宏观尺度的动态流变响应之间的精确相互作用仍然难以捉摸。在此,我们提出了一个基于机理的一般理论模型,该模型表明细胞骨架解离会产生一个随频率变化的损失模量峰值,而细胞质粘度会促进其恢复,并产生一个随后的低谷。我们定义了与交联剂解离率和细胞质粘度有关的两个特征频率(ωc1 和 ωc2),其中损耗模量(1)在 ωc1>ωc2 时呈现峰值和谷值,(2)在 ωc1>ωc2 时随频率单调增加。此外,由于解离率与应力有关,特征频率 ωc1 表现出与应力有关的双相行为,在足够高的应力下出现局部最小值。此外,特征频率ωc2随着年龄的增长而变化,呈幂律关系。DMM 模型的预测结果与实验观测结果十分吻合。我们的模型全面描述了细胞和类细胞材料的动态粘弹性行为。
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Characteristic frequencies of localized stress relaxation in scaling-law rheology of living cells.

Living cells are known to exhibit power-law viscoelastic responses and localized stress relaxation behaviors in frequency spectrum. However, the precise interplay between molecular scale cytoskeletal dynamics and macroscale dynamical rheological responses remains elusive. Here, we propose a mechanism-based general theoretical model showing that cytoskeleton dissociation generates a peak in the loss modulus as a function of frequency, while the cytoplasmic viscosity promotes its recovery, producing a subsequent trough. We define two characteristic frequencies ( ωc1 and ωc2 ) related to the dissociation rate of crosslinkers and the viscosity of the cytoplasm, where the loss modulus (1) exhibits peak and trough values for ωc1c2 , and (2) monotonically increases with frequency for ωc1c2. Furthermore, the characteristic frequency ωc1 exhibits a biphasic stress-dependent behavior, with a local minimum at sufficiently high stress due to the stress-dependent dissociation rate. Moreover, the characteristic frequency ωc2 evolves with age, following a power-law relationship. The predictions of the DMM model align well with experimental observations. Our model provides a comprehensive description of the dynamical viscoelastic behaviors of cells and cell-like materials.

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来源期刊
Biophysical journal
Biophysical journal 生物-生物物理
CiteScore
6.10
自引率
5.90%
发文量
3090
审稿时长
2 months
期刊介绍: BJ publishes original articles, letters, and perspectives on important problems in modern biophysics. The papers should be written so as to be of interest to a broad community of biophysicists. BJ welcomes experimental studies that employ quantitative physical approaches for the study of biological systems, including or spanning scales from molecule to whole organism. Experimental studies of a purely descriptive or phenomenological nature, with no theoretical or mechanistic underpinning, are not appropriate for publication in BJ. Theoretical studies should offer new insights into the understanding ofexperimental results or suggest new experimentally testable hypotheses. Articles reporting significant methodological or technological advances, which have potential to open new areas of biophysical investigation, are also suitable for publication in BJ. Papers describing improvements in accuracy or speed of existing methods or extra detail within methods described previously are not suitable for BJ.
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