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Speaker:
Prof.
Alex Mogilner The model consists of few 'modules':(i) polymerization ratchet model of protrusion, (ii) dynamic actin-myosin contraction model, (iii) dendritic-nucleation actin turnover model. We combine these models and simulate the cell as a 2-D domain with a free boundary using finite elements. The simulations reproduce the observed shapes and movements of the keratocyte cells and predict F-actin and G-actin densities.Comparing the computational and experimental results allows us to suggest the dynamic principles of spatio-temporal organization of cell movements and forces.
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