# Anisotropy and shear stress accumulation during collective migration of epithelial cells

**Authors:** Ivana Pajic-Lijakovic, Milan Milivojevic, Peter V. E. McClintock

PMC · DOI: 10.1007/s00249-026-01813-y · European Biophysics Journal · 2026-02-02

## TL;DR

This paper explores how anisotropy affects mechanical stress during epithelial cell migration and how cells might manage this stress.

## Contribution

The paper introduces a theoretical model of anisotropic viscoelasticity in migrating epithelial collectives and explores strategies to mitigate shear stress.

## Key findings

- Anisotropy contributes to mechanical stress accumulation during epithelial cell migration.
- Shear stress can disrupt cell adhesion and trigger inflammation and gene expression changes.
- Cellular strategies to mitigate shear stress involve trade-offs in energy and function.

## Abstract

Anisotropy is a fundamental physical characteristic that influences efficient cell migration in biological systems. Concurrently, anisotropy serves as a primary factor contributing to a significant accumulation of mechanical stress within migrating epithelial collectives, provided that the cells maintain the strong E-cadherin-mediated cell-cell adhesion contacts that are characteristic of epithelial cells. While cells are capable of effectively enduring both compressive and tensile stress, the shear stress that can be generated during a physiological process such as collective cell migration poses a risk of: (i) disrupting the adhesion contacts among cells and between cells and the extracellular matrix, (ii) causing a partial disintegration of the lipid bilayer and cytoskeleton, (iii) triggering cellular inflammation, and (iv) inducing changes in gene expression. The principal aims of this theoretical analysis are: (i) to emphasize the main characteristics of isotropic and anisotropic wetting/de-wetting of migrating epithelial collectives as the main factor in mechanical stress generation; (ii) to formulate a constitutive model of the anisotropic viscoelasticity of migrating epithelial and mesenchymal collectives; (iii) to emphasize the physical factors related to cell sensitivity to shear stress; and (iv) to explore potential cellular strategies to mitigate shear stress, while also highlighting the associated costs of these strategies.

## Linked entities

- **Proteins:** shg (shotgun)

## Full-text entities

- **Genes:** RAC1 (Rac family small GTPase 1) [NCBI Gene 403955] {aka RAC2}, LOC403934 (cell division cycle 42) [NCBI Gene 403934], CDH1 (cadherin 1) [NCBI Gene 999] {aka Arc-1, BCDS1, CD324, CDHE, ECAD, LCAM}, CDH2 (cadherin 2) [NCBI Gene 1000] {aka ACOGS, ADHD8, ARVD14, CD325, CDHN, CDw325}, CDH1 (cadherin 1) [NCBI Gene 442858] {aka Cadherin-1, Uvomorulin}
- **Diseases:** epithelial ovarian cancer (MESH:D000077216), inflammation (MESH:D007249), cancer (MESH:D009369)
- **Chemicals:** lipid (MESH:D008055)
- **Cell lines:** Hep-2 — Homo sapiens (Human), Human papillomavirus-related endocervical adenocarcinoma, Cancer cell line (CVCL_1906), HeLa — Homo sapiens (Human), Human papillomavirus-related endocervical adenocarcinoma, Cancer cell line (CVCL_0030), MDCK — Canis lupus familiaris (Dog), Spontaneously immortalized cell line (CVCL_0422)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12929303/full.md

## References

11 references — full list in the complete paper: https://tomesphere.com/paper/PMC12929303/full.md

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Source: https://tomesphere.com/paper/PMC12929303