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结合原子力显微镜和声学探头揭示活细胞弹性刚度张量的变化。

Combining AFM and acoustic probes to reveal changes in the elastic stiffness tensor of living cells.

作者信息

Nijenhuis Nadja, Zhao Xuegen, Carisey Alex, Ballestrem Christoph, Derby Brian

机构信息

School of Materials, Faculty of Engineering and Physical Sciences, Faculty of Life Sciences, University of Manchester, Manchester, United Kingdom; Wellcome Trust Centre for Cell-Matrix Research, Faculty of Life Sciences, University of Manchester, Manchester, United Kingdom.

School of Materials, Faculty of Engineering and Physical Sciences, Faculty of Life Sciences, University of Manchester, Manchester, United Kingdom.

出版信息

Biophys J. 2014 Oct 7;107(7):1502-12. doi: 10.1016/j.bpj.2014.07.073.

DOI:10.1016/j.bpj.2014.07.073
PMID:25296302
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4190602/
Abstract

Knowledge of how the elastic stiffness of a cell affects its communication with its environment is of fundamental importance for the understanding of tissue integrity in health and disease. For stiffness measurements, it has been customary to quote a single parameter quantity, e.g., Young's modulus, rather than the minimum of two terms of the stiffness tensor required by elasticity theory. In this study, we use two independent methods (acoustic microscopy and atomic force microscopy nanoindentation) to characterize the elastic properties of a cell and thus determine two independent elastic constants. This allows us to explore in detail how the mechanical properties of cells change in response to signaling pathways that are known to regulate the cell's cytoskeleton. In particular, we demonstrate that altering the tensioning of actin filaments in NIH3T3 cells has a strong influence on the cell's shear modulus but leaves its bulk modulus unchanged. In contrast, altering the polymerization state of actin filaments influences bulk and shear modulus in a similar manner. In addition, we can use the data to directly determine the Poisson ratio of a cell and show that in all cases studied, it is less than, but very close to, 0.5 in value.

摘要

了解细胞的弹性刚度如何影响其与周围环境的通讯,对于理解健康和疾病状态下的组织完整性至关重要。对于刚度测量,习惯上引用单一参数量,例如杨氏模量,而不是弹性理论所要求的刚度张量的至少两个项。在本研究中,我们使用两种独立方法(声学显微镜和原子力显微镜纳米压痕法)来表征细胞的弹性特性,从而确定两个独立的弹性常数。这使我们能够详细探究细胞的力学性质如何响应已知调节细胞细胞骨架的信号通路而发生变化。特别地,我们证明改变NIH3T3细胞中肌动蛋白丝的张力对细胞的剪切模量有强烈影响,但体积模量不变。相反,改变肌动蛋白丝的聚合状态以类似方式影响体积模量和剪切模量。此外,我们可以利用这些数据直接确定细胞的泊松比,并表明在所研究的所有情况下,其值均小于0.5但非常接近0.5。