Effect of F-actin and Microtubules on Cellular Mechanical Behavior Studied Using Atomic Force Microscope and an Image Recognition-Based Cytoskeleton Quantification Approach

被引:20
作者
Liu, Yi [1 ]
Mollaeian, Keyvan [1 ]
Shamim, Muhammad Huzaifah [2 ]
Ren, Juan [1 ]
机构
[1] Iowa State Univ, Dept Mech Engn, Ames, IA 50011 USA
[2] Rice Univ, Dept Elect & Comp Engn, Houston, TX 77005 USA
基金
美国国家科学基金会;
关键词
cell mechanics; F-actin; microtubules; image recognition-based cytoskeleton quantification; AFM; LIVING CELLS; FIBROBLASTS; FILAMENTS; DYNAMICS;
D O I
10.3390/ijms21020392
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cytoskeleton morphology plays a key role in regulating cell mechanics. Particularly, cellular mechanical properties are directly regulated by the highly cross-linked and dynamic cytoskeletal structure of F-actin and microtubules presented in the cytoplasm. Although great efforts have been devoted to investigating the qualitative relation between the cellular cytoskeleton state and cell mechanical properties, comprehensive quantification results of how the states of F-actin and microtubules affect mechanical behavior are still lacking. In this study, the effect of both F-actin and microtubules morphology on cellular mechanical properties was quantified using atomic force microscope indentation experiments together with the proposed image recognition-based cytoskeleton quantification approach. Young's modulus and diffusion coefficient of NIH/3T3 cells with different cytoskeleton states were quantified at different length scales. It was found that the living NIH/3T3 cells sense and adapt to the F-actin and microtubules states: both the cellular elasticity and poroelasticity are closely correlated to the depolymerization degree of F-actin and microtubules at all measured indentation depths. Moreover, the significance of the quantitative effects of F-actin and microtubules in affecting cellular mechanical behavior is depth-dependent.
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页数:14
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