TABLE 1.
Comparison of FEM and DEM modeling frameworks.
1) Cellular architecture is discrete | |||
| |||
FEM | DEM | ||
± | Representation of discrete tensegrity structure unclear | + | Can represent discrete tensegrity structure |
+ | Can be combined with DEM as a hybrid model | − | To keep computations tractable, number of components per cell is limited to a lumped version of the real cell layout |
| |||
2) Anisotropy also depends on cell geometry and network topology | |||
| |||
FEM | DEM | ||
+ | Finite elements can be adapted to cellular geometry | + | Discrete elements can be adapted to cellular geometry |
± | Incorporation of anisotropy of actin accumulation bundles to be understood | + | Anisotropy of actin accumulation bundles can easily be incorporated |
− | Computational issues related to modeling large scale cellular networks | + | Can scale to model large cellular networks and thus encompass their topological features |
| |||
3) Nonlinear and temporal mechanical characteristics | |||
| |||
FEM | DEM | ||
+ | Can be incorporated in finite elements | + | Can be incorporated in discrete elements |
− | May lead to heavy computations, even for average-sized cellular network | + | Nonlinear elasticity qualitatively resembles tissue deformation |
+ | Nonlinear elasticity contributes to model stability, prevents collapse | ||
− | Temporal characteristics can be computationally demanding | ||
| |||
4) Volume preservation | |||
| |||
FEM | DEM | ||
+ | Can be imposed through volumetric properties | ± | Its effect can be approximated but not formally embedded |
± | May result in artifacts and computational issues (stiffness), due to limited knowledge on properties of cell height | − | Approximation likely related to introduction of dynamical artifacts, requires evaluation of resulting mechanical properties |