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We introduce and theoretically investigate a minimal particle-based model for a new class of active matter where particles exhibit directional, volume-conserving division in confinement while interacting sterically, mimicking cells in early embryogenesis. We find that complex motion, synchronized within division cycles, displays strong collective effects and becomes self-similar in the long-time limit. Introducing the method of normalized retraced trajectories, we show that the transgenerational motion caused by cell division can be mapped to a time-inhomogenous random walk with an exponentially decreasing length scale. Analytical predictions for this stochastic process allow us to extract effective parameters, indicating unusual effects of crowding and absence of jamming. Robustness of our findings against desynchronized divisions, cell size dispersity, and variations in confinement hints at universal behavior. Our results establish an understanding of complex dynamics exhibited by isovolumentric division over long timescales, paving the way for new bioengineering strategies and perspectives on living matter., Comment: 9 pages, 3 figures

Replication through cell division is one of the most fundamental processes of life and a major driver of dynamics in systems ranging from bacterial colonies to embryogenesis, tissues and tumors. While regulation often plays a role in shaping self-organization, mounting evidence suggests that many biologically relevant behaviors exploit principles based on a limited number of physical ingredients, and particle-based models have become a popular platform to reconstitute and investigate these emergent dynamics. However, incorporating division into such models often leads to aberrant mechanical fluctuations that hamper physically meaningful analysis. Here, we present a minimal model focusing on mechanical consistency during division. Cells are comprised of two nodes, overlapping disks which separate from each other during cell division, resulting in transient dumbbell shapes. Internal degrees of freedom, cell-cell interactions and equations of motion are designed to ensure force continuity at all times, including through division, both for the dividing cell itself as well as interaction partners, while retaining the freedom to define arbitrary anisotropic mobilities. As a benchmark, we also translate an established model of proliferating spherocylinders with similar dynamics into our theoretical framework. Numerical simulations of both models demonstrate force continuity of the new disk cell model and quantify our improvements. We also investigate some basic collective behaviors related to alignment and orientational order and find consistency both between the models and with the literature. A reference implementation of the model is freely available as a package in the Julia programming language based on $\mathit{InPartS}$. Our model is ideally suited for the investigation of mechanical observables such as velocities and stresses, and is easily extensible with additional features., Comment: 18 pages, 6 figures

Growth is a known driver of cellular dynamics in a range of dense aggregates from bacterial colonies to developing tissues to tumors. Hence, universal physical principles underlying these dynamics are of great interdisciplinary interest. Here, we study the emergent dynamics arising from the interplay of growth, steric repulsion and motility in a minimal agent-based model of exponentially growing three-dimensional spheroids. Our results show that, without cell motility, deterministic motion caused by overall volume expansion dominates the dynamics of individual cells in the radial direction, while growth and division lead to cellular-scale diffusive motion in the tangential direction, whose magnitude is largely independent of expansion velocity. Despite this small-scale diffusion, we show that cell lineages are subject to confinement in their local environment, quenching weak cell motility. At higher motility, we find a transient regime of tangential superdiffusivity, which is accompanied by global mixing of cells. A quantitative analysis reveals a diverging mixing time scale at the transition, reminiscent of glassy dynamics. Our study highlights the complex interaction of local cell division and motility with global expansion, mediated exclusively by mechanics. The observations may serve as a baseline for the identification of phenomena caused by additional biological mechanisms in experiments on tissue spheroids, which have become a popular model system in biophysics and other fields. The mixing dynamics might also be relevant for competition or tumor progression., Comment: 9 pages, 4 figures, 8 supplementary figures, 5 supplementary videos

Motility coupled to responsive behavior is essential for many microorganisms to seek and establish appropriate habitats. One of the simplest possible responses, reversing the direction of motion, is believed to enable filamentous cyanobacteria to form stable aggregates or accumulate in suitable light conditions. Here, we demonstrate that filamentous morphology in combination with responding to light gradients by reversals has consequences far beyond simple accumulation: Entangled aggregates form at the boundaries of illuminated regions, harnessing the boundary to establish local order. We explore how the light pattern, in particular its boundary curvature, impacts aggregation. A minimal mechanistic model of active flexible filaments resembles the experimental findings, thereby revealing the emergent and generic character of these structures. This phenomenon may enable elongated microorganisms to generate adaptive colony architectures in limited habitats, or guide the assembly of biomimetic fibrous materials., Comment: 18 pages, 5 figures, 8 supplementary figures, 4 supplementary videos

Order and alignment are ubiquitous in growing colonies of rod-shaped bacteria due to the nematic properties of the constituent particles. These effects are the result of the active stresses generated by growth, passive mechanical interactions between cells, and flow-induced effects due to the shape of the confining container. However, how these contributing factors interact to give rise to the observed global alignment patterns remains elusive. Here, we study, in-silico, colonies of growing rod-shaped particles of different aspect ratios confined in channel-like geometries. A spatially resolved analysis of the stress tensor reveals a strong relationship between near-perfect alignment and an inversion of stress anisotropy for particles with large length-to-width ratios. We show that, in quantitative agreement with an asymptotic theory, strong alignment can lead to a decoupling of active and passive stresses parallel and perpendicular to the direction of growth, respectively. We demonstrate the robustness of these effects in a geometry that provides less restrictive confinement and introduces natural perturbations in alignment. Our results illustrate the complexity arising from the inherent coupling between nematic order and active stresses in growing active matter which is modulated by geometric and configurational constraints due to confinement., Comment: 9 pages, 5 figures