The potential for intercellular mechanical interaction: simulations of single chondrocyte versus anatomically based distribution

Biomechanics and Modeling in Mechanobiology(2017)

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Abstract
Computational studies of chondrocyte mechanics, and cell mechanics in general, have typically been performed using single cell models embedded in an extracellular matrix construct. The assumption of a single cell microstructural model may not capture intercellular interactions or accurately reflect the macroscale mechanics of cartilage when higher cell concentrations are considered, as may be the case in many instances. Hence, the goal of this study was to compare cell-level response of single and eleven cell biphasic finite element models, where the latter provided an anatomically based cellular distribution representative of the actual number of cells for a commonly used 100 m edge cubic representative volume in the middle zone of cartilage. Single cell representations incorporated a centered single cell model and eleven location-corrected single cell models, the latter to delineate the role of cell placement in the representative volume element. A stress relaxation test at 10
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Key words
Multi-scale,Computational modeling,Finite element,Cartilage,Chondrocyte,Poroelastic,Biphasic,Tissue mechanics,Cell mechanics,Homogenization
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