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. Author manuscript; available in PMC: 2013 Nov 1.
Published in final edited form as: Biomech Model Mechanobiol. 2012 Jul 7;11(8):1227–1239. doi: 10.1007/s10237-012-0419-2

Table 1. Contrasting features of a selection of myofibrillogenesis computation models.

Model property Novak et al. (2004) Deshpande et al. (2006, 2008) Paszek et al. (2009) Grosberg et al. (2011)
Model type Phenomeno-logical Finite element/solid mechanics Chemo-mechanical Phenomeno-logical
Model compared to cell type NIH3T3 fibroblasts (Brock et al. 2003) Retinal pigment epithelial human cells or fibroblast cells No specific cell type Neonatal rat ventricular myocytes
Integrins have a free and bound state (or high/low affinity) Yes Yes Yes Yes
Focal adhesions more stable with greater force Yes Yes Yes Yes
Myofibrils/stress fibers Yes Ye s No Yes
included in model Fiber length-force dependence No Not explicitly No Yes
Differentiating between pre-myofibril and nascent myofibril formation No No N/A Yes
Myofibril actively mutually align No No N/A Yes
Testing boundary conditions/symmetry breaking No No No Yes
Detailed model of solid mechanics of the interface No Yes Yes No
Substrate mechanical load No Yes, but not the deformation of the substrate Yes and Detailed, i.e. both stress and strain—deformation Yes, but very simply (only traction)
Computationally complex No Yes Yes No