Literature DB >> 26093345

Microscale consolidation analysis of relaxation behavior of single living chondrocytes subjected to varying strain-rates.

Trung Dung Nguyen1, Adekunle Oloyede1, Sanjleena Singh1, YuanTong Gu2.   

Abstract

Besides the elastic stiffness, the relaxation behavior of single living cells is also of interest of various researchers when studying cell mechanics. It is hypothesized that the relaxation response of the cells is governed by both intrinsic viscoelasticity of the solid phase and fluid-solid interactions mechanisms. There are a number of mechanical models have been developed to investigate the relaxation behavior of single cells. However, there is lack of model enable to accurately capture both of the mechanisms. Therefore, in this study, the porohyperelastic (PHE) model, which is an extension of the consolidation theory, combined with inverse Finite Element Analysis (FEA) technique was used at the first time to investigate the relaxation response of living chondrocytes. This model was also utilized to study the dependence of relaxation behavior of the cells on strain-rates. The stress-relaxation experiments under the various strain-rates were conducted with the Atomic Force Microscopy (AFM). The results have demonstrated that the PHE model could effectively capture the stress-relaxation behavior of the living chondrocytes, especially at intermediate to high strain-rates. Although this model gave some errors at lower strain-rates, its performance was acceptable. Therefore, the PHE model is properly a promising model for single cell mechanics studies. Moreover, it has been found that the hydraulic permeability of living chondrocytes reduced with decreasing of strain-rates. It might be due to the intracellular fluid volume fraction and the fluid pore pressure gradients of chondrocytes were higher when higher strain-rates applied.
Copyright © 2015 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  AFM; Cell biomechanics; Consolidation theory; Strain-rate dependent response

Mesh:

Year:  2015        PMID: 26093345     DOI: 10.1016/j.jmbbm.2015.05.003

Source DB:  PubMed          Journal:  J Mech Behav Biomed Mater        ISSN: 1878-0180


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