Confinement and substrate topography control cell migration in a 3D computational model

Benjamin Winkler, Igor Aronson, Falko Ziebert

Research output: Contribution to journalArticle

Abstract

Cell movement in vivo is typically characterized by strong confinement and heterogeneous, three-dimensional environments. Such external constraints on cell motility are known to play important roles in many vital processes e.g. during development, differentiation, and the immune response, as well as in pathologies like cancer metastasis. Here we develop a physics-driven three-dimensional computational modeling framework that describes lamellipodium-based motion of cells in arbitrarily shaped and topographically structured surroundings. We use it to investigate the primary in vitro model scenarios currently studied experimentally: motion in vertical confinement, confinement in microchannels, as well as motion on fibers and on imposed modulations of surface topography. We find that confinement, substrate curvature and topography modulate the cell’s speed, shape and actin organization and can induce changes in the direction of motion along axes defined by the constraints. Our model serves as a benchmark to systematically explore lamellipodium-based motility and its interaction with the environment.

Original languageEnglish (US)
Article number82
JournalCommunications Physics
Volume2
Issue number1
DOIs
StatePublished - Dec 1 2019

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topography
cells
locomotion
pathology
metastasis
microchannels
cancer
curvature
modulation
physics
fibers
interactions

All Science Journal Classification (ASJC) codes

  • Physics and Astronomy(all)

Cite this

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title = "Confinement and substrate topography control cell migration in a 3D computational model",
abstract = "Cell movement in vivo is typically characterized by strong confinement and heterogeneous, three-dimensional environments. Such external constraints on cell motility are known to play important roles in many vital processes e.g. during development, differentiation, and the immune response, as well as in pathologies like cancer metastasis. Here we develop a physics-driven three-dimensional computational modeling framework that describes lamellipodium-based motion of cells in arbitrarily shaped and topographically structured surroundings. We use it to investigate the primary in vitro model scenarios currently studied experimentally: motion in vertical confinement, confinement in microchannels, as well as motion on fibers and on imposed modulations of surface topography. We find that confinement, substrate curvature and topography modulate the cell’s speed, shape and actin organization and can induce changes in the direction of motion along axes defined by the constraints. Our model serves as a benchmark to systematically explore lamellipodium-based motility and its interaction with the environment.",
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Confinement and substrate topography control cell migration in a 3D computational model. / Winkler, Benjamin; Aronson, Igor; Ziebert, Falko.

In: Communications Physics, Vol. 2, No. 1, 82, 01.12.2019.

Research output: Contribution to journalArticle

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