Revealing the nanoindentation response of a single cell using a 3D structural finite element model

Changes in the apparent moduli of cells have been reported to correlate with cell abnormalities and disease. Indentation is commonly used to measure these moduli; however, there is evidence to suggest that the indentation protocol employed affects the measured moduli, which can affect our understanding of how physiological conditions regulate cell mechanics. Most studies treat the cell as a homogeneous material or a simple core-shell structure consisting of cytoplasm and a nucleus: both are far from the real structure of cells. To study indentation protocol-dependent cell mechanics, a finite element model of key intracellular components (cortex layer, cytoplasm, actin stress fibres, microtubules, and nucleus) has instead been developed. Results have shown that the apparent moduli obtained with conical indenters decreased with increasing cone angle; however, this change was less significant for spherical indenters of increasing radii. Furthermore, the interplay between indenter geometry and intracellular components has also been studied, which is useful for understanding structure-mechanics-function relationships of cells.

Automated summary

Changes in the apparent moduli of cells are related to cell abnormalities and diseases. Indentation is a common method used to measure these moduli, but the protocol employed can affect the results. A finite element model of key intracellular components has been developed to study indentation protocol-dependent cell mechanics, which has shown that the moduli obtained with conical indenters decrease with increasing cone angle. The interplay between indenter geometry and intracellular components has also been investigated for understanding the structure-mechanics-function relationships of cells.