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Liu, A. J.

Publications and source records attributed to Liu, A. J..

4 recordsLinked to original sources

Epithelial convergent extension as a tuning process

Self-tuning--the ability of disordered systems to develop desired collective behaviors by tuning internal couplings in response to feedback--has recently emerged as a powerful framework for understanding adaptation in amorphous solids, mechanical metamaterials, and electrical networks. These systems can learn desired responses, encode memory, and robustly reorganize under repeated stimuli, much like artificial neural networks but without requiring processors to adjust their weights. Here, we extend this paradigm to morphogenesis and show that the epithelium can be viewed as tunable matter and that epithelial convergent extension (CE) can be understood as a self-tuning process. Using a vertex model with active interfacial tensions, we systematically compare distinct tension-update strategies, including externally imposed shear, global gradient descent optimization, and decentralized local feedback rules. We find that while all methods can generate tissue elongation, only local orientation- and length-sensitive rules reproduce key experimental features of CE, such as supracellular actomyosin pattern formation, cell shape changes, and junctional alignment. In contrast, global optimization produces homogeneous tension patterns and mechanically fragile states. By interpreting CE through the lens of tuning, our framework bridges the physics of tunable matter with developmental biology, revealing how simple, local rules enable tissues to efficiently orchestrate complex morphogenetic outcomes through decentralized mechanical adaptation.

biophysics↗

Mechanosensitive Remodeling Sustains Rigidity Homeostasis in Actin Cortex Models

The actin cortex is a dynamic biopolymer network that, despite constant architectural changes through the assembly and disassembly of filaments and crosslinkers, sustains a rigid homeostatic state, i.e., a steady state of positive elastic moduli, and exhibits an elastic memory that far outlasts the structural turnover time scale. We still lack simple models that maintain collective rigidity and elastic memory at long times compared to the turnover time. To address this, we develop two complementary elastic network models in which rigidity homeostasis and long-lived elastic memory with complete turnover emerge as a result of mechanosensitive dynamics of filaments (edges) and crosslinkers (nodes), respectively. Both models require the following minimal ingredients: (1) preferential disassembly of edges or nodes under small tension or force, (2) a small but nonzero rate of random disassembly, and (3) energy injection upon assembly. Our models are robust to variations in random disassembly rates, can recover from drastic structural disruption, and exhibit diffusion of nodes and edges in steady state, displaying representational drift similar to that found in neuronal activities and physical learning circuits. We propose that the cortex is an example of "tunable matter," i.e., its mechanosensitive remodeling dynamics tune properties of its edges and nodes so that the cortex as a whole can maintain robust but flexible rigidity in fluctuating mechanical environments.

biophysics↗

Minimal vertex model explains how the amnioserosa avoids fluidization during Drosophila dorsal closure

Dorsal closure is a process that occurs during embryogenesis of Drosophila melanogaster. During dorsal closure, the amnioserosa (AS), a one-cell thick epithelial tissue that fills the dorsal opening, shrinks as the lateral epidermis sheets converge and eventually merge. During this process, both shape index and aspect ratio of amnioserosa cells increase markedly. The standard 2-dimensional vertex model, which successfully describes tissue sheet mechanics in multiple contexts, would in this case predict that the tissue should fluidize via cell neighbor changes. Surprisingly, however, the amnioserosa remains an elastic solid with no such events. We here present a minimal extension to the vertex model that explains how the amnioserosa can achieve this unexpected behavior. We show that continuous shrinkage of the preferred cell perimeter and cell perimeter polydispersity lead to the retention of the solid state of the amnioserosa. Our model accurately captures measured cell shape and orientation changes and predicts non-monotonic junction tension that we confirm with laser ablation experiments. Significance StatementDuring embryogenesis, cells in tissues can undergo significant shape changes. Many epithelial tissues fluidize, i.e. cells exchange neighbors, when the average cell shape index increases above a threshold value, consistent with the standard vertex model. During dorsal closure in Drosophila melanogaster, however, the amnioserosa tissue remains solid even as the average cell shape index increases well above threshold. We introduce perimeter polydispersity and allow the preferred cell perimeters, usually held fixed in vertex models, to decrease linearly with time as seen experimentally. With these extensions to the standard vertex model, we capture experimental observations quantitatively. Our results demonstrate that vertex models can describe the behavior of the amnioserosa in dorsal closure by allowing normally fixed parameters to vary with time.

biophysics↗

The Physical Effects of Learning

Interacting many-body physical systems ranging from neural networks in the brain to folding proteins to self-modifying electrical circuits can learn to perform specific tasks. This learning, both in nature and in engineered systems, can occur through evolutionary selection or through dynamical rules that drive active learning from experience. Here, we show that learning leaves architectural imprints on the Hessian of a physical system. Compared to a generic organization of the system components, (a) the effective physical dimension of the response to inputs (the participation ratio of low-eigenvalue modes) decreases, (b) the response of physical degrees of freedom to random perturbations (or system "susceptibility") increases, and (c) the low-eigenvalue eigenvectors of the Hessian align with the task. Overall, these effects suggest a method for discovering the task that a physical network may have been trained for.

biophysics↗