Epithelial Layer Fluidization by Curvature-Induced Unjamming

The transition of an epithelial layer from a stationary, quiescent state to a highly migratory, dynamic state is required for wound healing, development, and regeneration. This transition, known as the unjamming transition (UJT), is responsible for epithelial fluidization and collective migration. Previous theoretical models have primarily focused on the UJT in flat epithelial layers, neglecting the effects of strong surface curvature characteristic of the epithelium in vivo. In this Letter, we investigate the role of surface curvature on tissue plasticity and cellular migration using a vertex model embedded on a spherical surface. Our findings reveal that increasing curvature promotes the UJT by reducing the energy barriers to cellular rearrangements. Higher curvature favors cell intercalation, mobility, and self-diffusivity, resulting in epithelial structures that are malleable and migratory when small, but become more rigid and stationary as they grow. Together, these results provide a conceptual framework to better understand how cell shape, cell propulsion, and tissue geometry contribute to tissue malleability, remodeling, and stabilization.

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Publication Details

Journal
Physical Review Letters
Published
2025-04-03
DOI
https://doi.org/10.1103/physrevlett.134.138402
Citations
6
Primary Topic
Cellular Mechanics and Interactions
Type
article
Field-Weighted Citation Impact
6.91

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article

Epithelial Layer Fluidization by Curvature-Induced Unjamming

Dapeng Bi, Amit Das, Jeffrey J. Fredberg, Margherita De Marzio
6 citations
Physical Review Letters
Cellular Mechanics and Interactions
6.91
article

Epithelial Layer Fluidization by Curvature-Induced Unjamming

Dapeng Bi, Amit Das, Jeffrey J. Fredberg, Margherita De Marzio
article en
6 citations

Abstract

The transition of an epithelial layer from a stationary, quiescent state to a highly migratory, dynamic state is required for wound healing, development, and regeneration. This transition, known as the unjamming transition (UJT), is responsible for epithelial fluidization and collective migration. Previous theoretical models have primarily focused on the UJT in flat epithelial layers, neglecting the effects of strong surface curvature characteristic of the epithelium in vivo. In this Letter, we investigate the role of surface curvature on tissue plasticity and cellular migration using a vertex model embedded on a spherical surface. Our findings reveal that increasing curvature promotes the UJT by reducing the energy barriers to cellular rearrangements. Higher curvature favors cell intercalation, mobility, and self-diffusivity, resulting in epithelial structures that are malleable and migratory when small, but become more rigid and stationary as they grow. Together, these results provide a conceptual framework to better understand how cell shape, cell propulsion, and tissue geometry contribute to tissue malleability, remodeling, and stabilization.

Physical Review LettersVol. 134(13)
Brigham and Women's Hospital (US), Harvard University (US), Indian Institute of Technology Delhi (IN), Universidad del Noreste (MX)
National Science Foundation, Alfred P. Sloan Foundation, Human Frontier Science Program, Department of Science and Technology, Ministry of Science and Technology, India, Indian Institute of Technology Delhi, National Institutes of Health, Science and Engineering Research Board, National Heart, Lung, and Blood Institute, National Institute of General Medical Sciences
Climate action
Openalex Percentile: Top 3%
Cellular Mechanics and Interactions
6.91
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