From energy to cellular forces in the Cellular Potts Model: An algorithmic approach.

Single and collective cell dynamics, cell shape changes, and cell migration can be conveniently represented by the Cellular Potts Model, a computational platform based on minimization of a Hamiltonian. Using the fact that a force field is easily derived from a scalar energy (F = -∇H), we develop a s...

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Main Authors: Elisabeth G Rens, Leah Edelstein-Keshet
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-12-01
Series:PLoS Computational Biology
Online Access:https://doi.org/10.1371/journal.pcbi.1007459
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spelling doaj-d5e6f1d111bc4273b20d27974db716352021-04-21T15:12:45ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582019-12-011512e100745910.1371/journal.pcbi.1007459From energy to cellular forces in the Cellular Potts Model: An algorithmic approach.Elisabeth G RensLeah Edelstein-KeshetSingle and collective cell dynamics, cell shape changes, and cell migration can be conveniently represented by the Cellular Potts Model, a computational platform based on minimization of a Hamiltonian. Using the fact that a force field is easily derived from a scalar energy (F = -∇H), we develop a simple algorithm to associate effective forces with cell shapes in the CPM. We predict the traction forces exerted by single cells of various shapes and sizes on a 2D substrate. While CPM forces are specified directly from the Hamiltonian on the cell perimeter, we approximate the force field inside the cell domain using interpolation, and refine the results with smoothing. Predicted forces compare favorably with experimentally measured cellular traction forces. We show that a CPM model with internal signaling (such as Rho-GTPase-related contractility) can be associated with retraction-protrusion forces that accompany cell shape changes and migration. We adapt the computations to multicellular systems, showing, for example, the forces that a pair of swirling cells exert on one another, demonstrating that our algorithm works equally well for interacting cells. Finally, we show forces exerted by cells on one another in classic cell-sorting experiments.https://doi.org/10.1371/journal.pcbi.1007459
collection DOAJ
language English
format Article
sources DOAJ
author Elisabeth G Rens
Leah Edelstein-Keshet
spellingShingle Elisabeth G Rens
Leah Edelstein-Keshet
From energy to cellular forces in the Cellular Potts Model: An algorithmic approach.
PLoS Computational Biology
author_facet Elisabeth G Rens
Leah Edelstein-Keshet
author_sort Elisabeth G Rens
title From energy to cellular forces in the Cellular Potts Model: An algorithmic approach.
title_short From energy to cellular forces in the Cellular Potts Model: An algorithmic approach.
title_full From energy to cellular forces in the Cellular Potts Model: An algorithmic approach.
title_fullStr From energy to cellular forces in the Cellular Potts Model: An algorithmic approach.
title_full_unstemmed From energy to cellular forces in the Cellular Potts Model: An algorithmic approach.
title_sort from energy to cellular forces in the cellular potts model: an algorithmic approach.
publisher Public Library of Science (PLoS)
series PLoS Computational Biology
issn 1553-734X
1553-7358
publishDate 2019-12-01
description Single and collective cell dynamics, cell shape changes, and cell migration can be conveniently represented by the Cellular Potts Model, a computational platform based on minimization of a Hamiltonian. Using the fact that a force field is easily derived from a scalar energy (F = -∇H), we develop a simple algorithm to associate effective forces with cell shapes in the CPM. We predict the traction forces exerted by single cells of various shapes and sizes on a 2D substrate. While CPM forces are specified directly from the Hamiltonian on the cell perimeter, we approximate the force field inside the cell domain using interpolation, and refine the results with smoothing. Predicted forces compare favorably with experimentally measured cellular traction forces. We show that a CPM model with internal signaling (such as Rho-GTPase-related contractility) can be associated with retraction-protrusion forces that accompany cell shape changes and migration. We adapt the computations to multicellular systems, showing, for example, the forces that a pair of swirling cells exert on one another, demonstrating that our algorithm works equally well for interacting cells. Finally, we show forces exerted by cells on one another in classic cell-sorting experiments.
url https://doi.org/10.1371/journal.pcbi.1007459
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