The European network

for cell migration studies

This project has received funding from the European Union’s Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant agreement No 642866.

incem@rwth-aachen.de

Advanced cell migration assays (P1)

12 - Life time models

A typical example of the application of the evolving surface finite element method when solving partial differential equations of reaction-diffusion type on an evolving closed surface representing an evolving tumour. The evolving surface finite element is a powerful numerical method for approximating numerical solutions of systems of partial differential equations routinely encounter in cell biology where for example, the cell surface is continuously evolving. Here we exhibit how the tumour is evolving where the surface evolution law is driven by chemical concentrations.

Based on experimentally observed structures, we will develop and adapt current mathematical models of reaction-diffusion type (in 2D, 3D, on surfaces) to describe the spatio-temporal life cycles of actin and keratin filaments, their binding proteins, focal adhesions, hemidesmosomes and various regulatory molecules. We propose to adapt reaction models for actin and keratin filaments to describe biochemical processes such as nucleation, polymerisation and solubilisation, depolymerisation, annealing, disassembly and fragmentation and extend the models to take into account diffusion processes. To further understand migrating single cells, we will mathematically characterise the morphology and dynamics of FAs by modelling their size, number, localisation, velocity profiles and turnover. We will develop new mathematical models to describe hemidesmosome protein dynamics. The models derived will be solved efficiently, accurately and robustly by the use of moving and surface finite element methods in 2- and 3-D and on complex evolving topological surfaces. Ultimately, we will develop an integrated computational model to link the dependencies between the individual components of the life cycle.

Real-time tracking of keratinocyte migration and analysis of cell membrane shape changes (P10)

Speckle analysis of actin and keratin filament dynamics (P11)

Life time models (P12)

Shaping membranes and actin fibres by forces (P13)

Model validation - integrating shape change models and imaging (P14)

Integration of forces and life times (P15)

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Last update: 18.04.2016