TY - JOUR
T1 - A mesoscale mechanical model of cellular interactions
AU - DiNapoli, Kathleen T.
AU - Robinson, Douglas N.
AU - Iglesias, Pablo A.
N1 - Publisher Copyright:
© 2021 Biophysical Society
PY - 2021/11/16
Y1 - 2021/11/16
N2 - Computational models of cell mechanics allow the precise interrogation of cell shape change. These morphological changes are required for cells to survive in diverse tissue environments. Here, we present a mesoscale mechanical model of cell-substrate interactions using the level set method based on experimentally measured parameters. By implementing a viscoelastic mechanical equivalent circuit, we accurately model whole-cell deformations that are important for a variety of cellular processes. To effectively model shape changes as a cell interacts with a substrate, we have included receptor-mediated adhesion, which is governed by catch-slip bond behavior. The effect of adhesion was explored by subjecting cells to a variety of different substrates including flat, curved, and deformable surfaces. Finally, we increased the accuracy of our simulations by including a deformable nucleus in our cells. This model sets the foundation for further exploration into computational analyses of multicellular interactions.
AB - Computational models of cell mechanics allow the precise interrogation of cell shape change. These morphological changes are required for cells to survive in diverse tissue environments. Here, we present a mesoscale mechanical model of cell-substrate interactions using the level set method based on experimentally measured parameters. By implementing a viscoelastic mechanical equivalent circuit, we accurately model whole-cell deformations that are important for a variety of cellular processes. To effectively model shape changes as a cell interacts with a substrate, we have included receptor-mediated adhesion, which is governed by catch-slip bond behavior. The effect of adhesion was explored by subjecting cells to a variety of different substrates including flat, curved, and deformable surfaces. Finally, we increased the accuracy of our simulations by including a deformable nucleus in our cells. This model sets the foundation for further exploration into computational analyses of multicellular interactions.
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U2 - 10.1016/j.bpj.2021.10.021
DO - 10.1016/j.bpj.2021.10.021
M3 - Article
C2 - 34687718
AN - SCOPUS:85118535033
SN - 0006-3495
VL - 120
SP - 4905
EP - 4917
JO - Biophysical journal
JF - Biophysical journal
IS - 22
ER -