Origin of yield stress and mechanical plasticity in model biological tissues

During development and under normal physiological conditions, biological tissues are continuously subjected to substantial mechanical stresses. In response to large deformations, cells in a tissue must undergo multicellular rearrangements to maintain integrity and robustness. However, how these events are connected in time and space remains unknown. Here, using theoretical modeling, we study the mechanical plasticity of cell monolayers under large deformations. Our results suggest that the jamming-unjamming (solid-fluid) transition can vary significantly depending on the degree of deformation, implying that tissues are highly unconventional materials. We elucidate the origins of this behavior. We also demonstrate how large deformations are accommodated through a series of cellular rearrangements, similar to avalanches in non-living materials. We find that these 'tissue avalanches' are governed by stress redistribution and the spatial distribution of "soft" or vulnerable spots, which are more prone to undergo rearrangements. Finally, we propose a simple and experimentally accessible framework to infer tissue-level stress and predict avalanches based on static images.

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Publication Details

Journal
Nature Communications
Published
2025-04-05
DOI
https://doi.org/10.1038/s41467-025-58526-7
Citations
4
Primary Topic
Cellular Mechanics and Interactions
Type
article
Field-Weighted Citation Impact
4.61

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article

Origin of yield stress and mechanical plasticity in model biological tissues

Dapeng Bi, Junxiang Huang, Anh Q. Nguyen
4 citations
Nature Communications
Cellular Mechanics and Interactions
4.61
article

Origin of yield stress and mechanical plasticity in model biological tissues

Dapeng Bi, Junxiang Huang, Anh Q. Nguyen
article en
4 citations

Abstract

During development and under normal physiological conditions, biological tissues are continuously subjected to substantial mechanical stresses. In response to large deformations, cells in a tissue must undergo multicellular rearrangements to maintain integrity and robustness. However, how these events are connected in time and space remains unknown. Here, using theoretical modeling, we study the mechanical plasticity of cell monolayers under large deformations. Our results suggest that the jamming-unjamming (solid-fluid) transition can vary significantly depending on the degree of deformation, implying that tissues are highly unconventional materials. We elucidate the origins of this behavior. We also demonstrate how large deformations are accommodated through a series of cellular rearrangements, similar to avalanches in non-living materials. We find that these 'tissue avalanches' are governed by stress redistribution and the spatial distribution of "soft" or vulnerable spots, which are more prone to undergo rearrangements. Finally, we propose a simple and experimentally accessible framework to infer tissue-level stress and predict avalanches based on static images.

Nature CommunicationsVol. 16(1)
Northeastern University (US), Center for Theoretical Biological Physics (US)
National Science Foundation, Alfred P. Sloan Foundation, Human Frontier Science Program, National Institutes of Health, National Institute of General Medical Sciences, Division of Materials Research
Zero hunger
Openalex Percentile: Top 6%
Cellular Mechanics and Interactions
4.61
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Origin of yield stress and mechanical plasticity in model biological tissues — Dapeng Bi, Junxiang Huang, et al. · Nature Communications (2025) | TGRS Research Map | TGRS