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Cell Rep ; 27(6): 1897-1909.e4, 2019 05 07.
Article in English | MEDLINE | ID: mdl-31067472

ABSTRACT

Three-dimensional matrices often contain highly structured adhesive tracks that require cells to turn corners and bridge non-adhesive areas. Here, we investigate these complex processes using micropatterned cell adhesive frames. Spreading kinetics on these matrices depend strongly on initial adhesive position and are predicted by a cellular Potts model (CPM), which reflects a balance between adhesion and intracellular tension. As cells spread, new stress fibers (SFs) assemble periodically and parallel to the leading edge, with spatial intervals of ∼2.5 µm, temporal intervals of ∼15 min, and characteristic lifetimes of ∼50 min. By incorporating these rules into the CPM, we can successfully predict SF network architecture. Moreover, we observe broadly similar behavior when we culture cells on arrays of discrete collagen fibers. Our findings show that ECM geometry and initial cell position strongly determine cell spreading and that cells encode a memory of their spreading history through SF network organization.


Subject(s)
Cell Movement , Extracellular Matrix/metabolism , Stress Fibers/metabolism , Actin Cytoskeleton/drug effects , Actin Cytoskeleton/metabolism , Cell Adhesion/drug effects , Cell Line, Tumor , Cell Movement/drug effects , Collagen/metabolism , Computer Simulation , Extracellular Matrix/drug effects , Half-Life , Heterocyclic Compounds, 4 or More Rings/pharmacology , Humans , Kinetics , Models, Biological , Pseudopodia/drug effects , Pseudopodia/metabolism , Stress Fibers/drug effects , Time Factors
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