The simulation of stress fibre and focal adhesion development in cells on patterned substrates
Author(s) -
Amit Pathak,
V.S. Deshpande,
Robert M. McMeeking,
A.G. Evans
Publication year - 2007
Publication title -
journal of the royal society interface
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.655
H-Index - 139
eISSN - 1742-5689
pISSN - 1742-5662
DOI - 10.1098/rsif.2007.1182
Subject(s) - cytoskeleton , stress fiber , focal adhesion , ligand (biochemistry) , biophysics , adhesion , myosin , actin , curvature , stress (linguistics) , actin cytoskeleton , materials science , tension (geology) , chemistry , pattern formation , nanotechnology , geometry , composite material , cell , biology , receptor , biochemistry , mathematics , linguistics , philosophy , genetics , ultimate tensile strength
The remodelling of the cytoskeleton and focal adhesion (FA) distributions for cells on substrates with micro-patterned ligand patches is investigated using a bio-chemo-mechanical model. We investigate the effect of ligand pattern shape on the cytoskeletal arrangements and FA distributions for cells having approximately the same area. The cytoskeleton model accounts for the dynamic rearrangement of the actin/myosin stress fibres. It entails the highly nonlinear interactions between signalling, the kinetics of tension-dependent stress-fibre formation/dissolution and stress-dependent contractility. This model is coupled with another model that governs FA formation and accounts for the mechano-sensitivity of the adhesions from thermodynamic considerations. This coupled modelling scheme is shown to capture a variety of key experimental observations including: (i) the formation of high concentrations of stress fibres and FAs at the periphery of circular and triangular, convex-shaped ligand patterns; (ii) the development of high FA concentrations along the edges of the V-, T-, Y- and U-shaped concave ligand patterns; and (iii) the formation of highly aligned stress fibres along the non-adhered edges of cells on the concave ligand patterns. When appropriately calibrated, the model also accurately predicts the radii of curvature of the non-adhered edges of cells on the concave-shaped ligand patterns.
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