ReviewEuropean biophysics journal : EBJ2026
Anisotropy and shear stress accumulation during collective migration of epithelial cells.
Review in European biophysics journal : EBJ, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- What is active wetting?The European physical journal. E, Soft matter · 2026Review
Corrections and comments
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Authors and funding
3 authors.
Funding
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.
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