Institute of Nuclear Physics Polish Academy of Sciences, Krakow PL-31-342, Poland.
Department of Physiology, and Institute for Medicine and Engineering, University of Pennsylvania, Philadelphia, Pennsylvania 19104-6383, United States.
Nano Lett. 2022 Jun 22;22(12):4725-4732. doi: 10.1021/acs.nanolett.2c00736. Epub 2022 Jun 9.
In this work, we investigate whether stiffening in compression is a feature of single cells and whether the intracellular polymer networks that comprise the cytoskeleton (all of which stiffen with increasing shear strain) stiffen or soften when subjected to compressive strains. We find that individual cells, such as fibroblasts, stiffen at physiologically relevant compressive strains, but genetic ablation of vimentin diminishes this effect. Further, we show that unlike networks of purified F-actin or microtubules, which soften in compression, vimentin intermediate filament networks stiffen in both compression and extension, and we present a theoretical model to explain this response based on the flexibility of vimentin filaments and their surface charge, which resists volume changes of the network under compression. These results provide a new framework by which to understand the mechanical responses of cells and point to a central role of intermediate filaments in response to compression.
在这项工作中,我们研究了压缩变硬是否是单细胞的特征,以及构成细胞骨架的细胞内聚合物网络(随着剪切应变的增加而变硬)在受到压缩应变时是变硬还是变软。我们发现,单个细胞(如成纤维细胞)在生理相关的压缩应变下变硬,但去除波形蛋白会减弱这种效应。此外,我们还表明,与在压缩时变软的纯化 F-肌动蛋白或微管网络不同,波形蛋白中间丝网络在压缩和拉伸时都会变硬,我们提出了一个理论模型来解释这种响应,该模型基于波形蛋白丝的柔韧性及其表面电荷,这些电荷在网络受到压缩时抵抗网络的体积变化。这些结果提供了一个理解细胞力学响应的新框架,并指出中间丝在响应压缩方面起着核心作用。