Discrete viscoelastic model of deformable immune cell migration through confined tumor microchannels

Abstract Understanding the mechanical behavior of immune cells as they migrate through the complex environment of solid tumors may be crucial for improving immunotherapy strategies. In this work, we present a particle-based model that captures the large deformations of single immune cells migrating through confined microchannels, which mimic the narrow tumor micropores. In our model, the nucleus, cytoplasm, and membrane are simulated through discrete particles with varying interacting forces that account for the differences in the mechanical properties of the discrete parts of the cell. We compare and validate the model with experimental measurements from microfluidic devices, providing relevant mechanistic conclusions into the effects of changes in cellular stiffness on migration efficiency.

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Publication Details

Journal
npj Systems Biology and Applications
Published
2026-11-07
DOI
https://doi.org/10.1038/s41540-026-00843-8
Primary Topic
Cellular Mechanics and Interactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Discrete viscoelastic model of deformable immune cell migration through confined tumor microchannels

Daniel Camacho-Gómez, Jack Zhang-Zhou, Jose Manuel Garcia-Aznar, David Garcia-Navarro
1 links
npj Systems Biology and Applications
Cellular Mechanics and Interactions
article

Discrete viscoelastic model of deformable immune cell migration through confined tumor microchannels

Daniel Camacho-Gómez, Jack Zhang-Zhou, Jose Manuel Garcia-Aznar, David Garcia-Navarro
article en

Abstract

Abstract Understanding the mechanical behavior of immune cells as they migrate through the complex environment of solid tumors may be crucial for improving immunotherapy strategies. In this work, we present a particle-based model that captures the large deformations of single immune cells migrating through confined microchannels, which mimic the narrow tumor micropores. In our model, the nucleus, cytoplasm, and membrane are simulated through discrete particles with varying interacting forces that account for the differences in the mechanical properties of the discrete parts of the cell. We compare and validate the model with experimental measurements from microfluidic devices, providing relevant mechanistic conclusions into the effects of changes in cellular stiffness on migration efficiency.

npj Systems Biology and Applications
Universidad de Zaragoza (ES), Moffitt Cancer Center (US), Instituto de Investigación en Ingeniería de Aragón (ES)
European Commission, H2020 European Research Council
Good health and well-being
Openalex Percentile: Top 99%
Cellular Mechanics and Interactions
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