arXiv subjects

Valeriia Grudtsyna

Publications and source records attributed to Valeriia Grudtsyna.

4 recordsLinked to original sources

arXiv2026

Epithelia Realize Nematopolar Topological Defect Structures

We introduce a shape-based polar order parameter that captures the structural asymmetry of cells within epithelial monolayers. By combining bright-field imaging and traction force microscopy, we demonstrate that shape polarity serves as a unifying biomechanical metric, integrating the physical information encoded by nematic directors, principal stresses, and cellular motion. Furthermore, we show that the tissue organizes into a mixed polar-nematic phase, characterized by the coexistence of integer ($\pm 1$) and half-integer ($\pm 1/2$) defects. Through mechanical perturbations, we demonstrate that both substrate stiffness and cell-cell adhesion modulate the density of these excitations and the length of domain walls binding like-signed positive half-integer defects. Using a minimal continuum model of polar-nematic active matter, we establish that this mixed phase is fundamentally driven by the interplay of active stresses and polar-nematic elasticity. These findings provide a direct experimental evidence that epithelial monolayers behave as nematopolar matter, in which coupled polar and nematic elastic interactions jointly shape the active state

cond-mat.soft↗

arXiv2025

A spectrum of p-atic symmetries and defects in confluent epithelia

Topological defects provide a unifying language to describe how orientational order breaks down in active and living matter. Considering cells as elongated particles confluent, epithelial tissues can be interpreted as nematic fields and its defects have been linked to extrusion, migration, and morphogenetic transformations. Yet, epithelial cells are not restricted to nematic order: their irregular shapes can express higher rotational symmetries, giving rise to p-atic order. Here we introduce a framework to extract p-atic fields and their defects directly from experimental images. Applying this method to MDCK cells, we find that all symmetries generate defects.No strong positional or orientational correlations are found between nematic and hexatic defects, suggesting that different symmetries coexist largely independently. These results demonstrate that epithelial tissues should not be described by nematic order alone, but instead host a spectrum of p-atic symmetries. Our work provides the first direct experimental evidence for this multivalency of order and offers a route to test and refine emerging p-atic liquid crystal theories of living matter.

cond-mat.soft↗

arXiv2025

Cellular Flow Architecture Exposes the Hidden Mechanics of Biological Matter

Understanding how biomechanical reorganization governs key biological processes, such as morphogenesis and development, requires predictive insights into stress distributions and cellular behavior. While traditional approaches focused on cell motion as a response to stress, we demonstrate that Lagrangian coherent structures (LCSs) -- robust attractors and repellers in cellular flows -- precede and drive long-term intercellular stress reorganization, physically governed by the mechanical properties of intercellular junctions. We show that this hidden flow skeleton correlates strongly with biomechanical metrics, bridging microscopic cell motion with mesoscopic biomechanics. Specifically, attractors and repellers mark hotspots of compressive and tensile stress enrichment (exceeding tenfold), alongside heterogeneities in cell packing. Notably, these connections remain robust across varying strengths of cell-cell and cell-substrate force transmission. Finally, by linking the attracting regions in the flow skeleton to future cell extrusion spots, we establish a direct link between cell motion and biologically significant outcomes. Together, these findings establish a framework for using cell motion to independently infer biomechanical metrics and bridge the scale mismatch between cell motion and biomechanics, potentially offering a new route to interpret mechanosensitive biological processes directly from cell trajectories.

physics.bio-ph↗

arXiv2024

Evidence of robust, universal conformal invariance in living biological matter

Collective cellular movement plays a crucial role in many processes fundamental to health, including development, reproduction, infection, wound healing, and cancer. The emergent dynamics that arise in these systems are typically thought to depend on how cells interact with one another and the mechanisms used to drive motility, both of which exhibit remarkable diversity across different biological systems. Here, we report experimental evidence of a universal feature in the patterns of flow that spontaneously emerges in groups of collectively moving cells. Specifically, we demonstrate that the flows generated by collectively moving dog kidney cells, human breast cancer cells, and by two different strains of pathogenic bacteria, all exhibit conformal invariance. Remarkably, not only do our results show that all of these very different systems display robust conformal invariance, but we also discovered that the precise form of the invariance in all four systems is described by the Schramm-Loewner Evolution (SLE), and belongs to the percolation universality class. A continuum model of active matter can recapitulate both the observed conformal invariance and SLE form found in experiments. The presence of universal conformal invariance reveals that the macroscopic features of living biological matter exhibit universal translational, rotational, and scale symmetries that are independent of the microscopic properties of its constituents. Our results show that the patterns of flows generated by diverse cellular systems are highly conserved and that biological systems can unexpectedly be used to experimentally test predictions from the theories for conformally invariant structures

cond-mat.soft↗