Skip to main content
. 2013 Nov 21;9(11):e1003319. doi: 10.1371/journal.pcbi.1003319

Table 1. CC3D parameters that were varied in the model and their biological significance in branching morphogenesis and cleft formation.

CC3D parameters to vary Biological effect simulated Experimental data - Effect seen in cleft formation Unknown biological effects
Focal point plasticity λ (FPP λ) Actin-myosin contractility in the cleft cells Decreasing contractility prevents initiated clefts from progressing [6] Increasing contractility.Increasing or decreasing contractility within cleft region
Mitosis rate (MR) Epithelial cell proliferation – in outer columnar cells (OCC) and inner polymorphic cells (IPC) Decreasing cell proliferation in the whole organ decreased cleft progression but not initiation [6] Increasing mitosis rate.Varying mitosis rates in specific subsets of cells in OCC and IPC populations.
Cell-cell (CC) contact energy E-cadherin-based cell-cell junctions E-cadherin mRNA was found to be ∼6 fold lower in the cleft epithelium than in the bud epithelium [10] Global reduction of E-cadherin decreases branching morphogenesis [38] Increasing E-cadherin protein activity.Increasing or decreasing E-cadherin levels in the cleft region
Cell-matrix (CM) contact energy Cell-matrix adhesions Decreased FN decreases cleft formation [5]. Lower FN assembly reduces cleft depth [22] Increasing FN assembly levels in the cleft region