Training Stress Patterns in 3D Cellular Packings
Oral-In-person
Abstract
Cells and tissues adapt to mechanical stimuli through feedback mechanisms to reorganize their internal stresses. Inspired by this biological adaptability, we investigate the possibility of training cell-level stress patterns in cellular packings with rearrangements. Specifically, we develop a contrastive learning algorithm for the 3D vertex model, in which iterative updates to the preferred shape indices (sā) of hidden (non-target) cells are applied to achieve a prescribed maximum shear stress on target cells with high precision.
We show that the algorithm reliably trains a single target cell to reach large deviations from its initial stress state. During successful training, the distribution of hidden-cell shape parameters drifts coherently, solidifying for high target stresses and fluidizing for low ones. This reveals a compatibility constraint: multi-cell targets must converge toward a common stress level. Under this constraint, multi-cell stress patterns are also trainable; however, the number of target cells that can be trained is limited by the number of hidden cells, defining a mechanical capacity for stress learning. Finally, we demonstrate multi-pattern adaptability, in which alternating between two target patterns progressively reduces the switching cost.
Introducing such physical learning algorithms into tissue models may provide a framework for understanding how tumor spheroids and other active collectives program cell-level stresses to drive invasion or morphogenesis.
We show that the algorithm reliably trains a single target cell to reach large deviations from its initial stress state. During successful training, the distribution of hidden-cell shape parameters drifts coherently, solidifying for high target stresses and fluidizing for low ones. This reveals a compatibility constraint: multi-cell targets must converge toward a common stress level. Under this constraint, multi-cell stress patterns are also trainable; however, the number of target cells that can be trained is limited by the number of hidden cells, defining a mechanical capacity for stress learning. Finally, we demonstrate multi-pattern adaptability, in which alternating between two target patterns progressively reduces the switching cost.
Introducing such physical learning algorithms into tissue models may provide a framework for understanding how tumor spheroids and other active collectives program cell-level stresses to drive invasion or morphogenesis.
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Publication: Training Stress Patterns in 3D Cellular Packings; Shabeeb Ameen, Tao Zhang, J.M. Schwarz (in preparation)
Presenters
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Shabeeb Ameen
- Syracuse University