Active Tension Network model reveals an exotic mechanical state realized in epithelial tissues

TL;DR

This paper introduces the Active Tension Network model, a novel theoretical framework that captures the active, tension-driven mechanics of epithelial tissues, explaining cell deformation and stress distribution during morphogenesis.

Contribution

The paper formulates and analyzes an Active Tension Network model based on tension-dominated mechanics and tension-dependent remodeling, providing new insights into epithelial tissue behavior.

Findings

Stationary ATN configurations form a one-parameter manifold per cell.

Isogonal deformations account for ~90% of cell shape changes during ventral furrow formation.

The model predicts exponential stress screening and negative Poisson ratio responses.

Abstract

It is now widely recognized that mechanical interactions between cells play a crucial role in epithelial morphogenesis, yet understanding the mechanisms through which stress and deformation affect cell behavior remains an open problem due to the complexity inherent in the mechanical behavior of cells and the difficulty of direct measurement of forces within tissues. Theoretical models can help by focusing experimental studies and by providing the framework for interpreting measurements. To that end, "vertex models" have introduced an approximation of epithelial cell mechanics based on a polygonal tiling representation of planar tissue. Here we formulate and analyze an Active Tension Network (ATN) model, which is based on the same polygonal representation of epithelial tissue geometry, but in addition i) assumes that mechanical balance is dominated by cortical tension and ii) introduces tension dependent local remodeling of the cortex, representing the active nature of cytoskeletal mechanics. The tension-dominance assumption has immediate implications for the geometry of cells, which we demonstrate to hold in certain types of Drosophila epithelial tissues. We demonstrate that stationary configurations of an ATN form a manifold with one degree of freedom per cell, corresponding to "isogonal" - i.e. angle preserving - deformations of cells, which dominate the dynamic response to perturbations. We show that isogonal modes account for approximately 90% of experimentally observed deformation of cells during the process of ventral furrow formation in Drosophila. Other interesting properties of our model include the exponential screening of mechanical stress and a negative Poisson ratio response to external uniaxial stress. We also provide a new approach to the problem of inferring local cortical tensions from the observed geometry of epithelial cells in a tissue