Coarsening dynamics of chemotactic aggregates
arXiv:2409.20100 · doi:10.1103/c9px-mdhs
Abstract
Auto-chemotaxis, the directed movement of cells along gradients in chemicals they secrete, is central to the formation of complex spatiotemporal patterns in biological systems. Since the introduction of the Keller--Segel model, numerous variants have been analyzed, revealing phenomena such as coarsening of aggregates, stable aggregate sizes, and spatiotemporally chaotic dynamics. Here, we consider general mass-conserving Keller--Segel models, that is, models without cell growth and death, and analyze the generic long-time dynamics of the chemotactic aggregates. Building on and extending our previous work, which demonstrated that chemotactic aggregation can be understood through a generalized Maxwell construction balancing density fluxes and reactive turnover, we use singular perturbation theory to derive the rates of mass competition between well-separated aggregates. We analyze how this mass-competition process drives coarsening in both diffusion- and reaction-limited regimes, with the diffusion-limited rate aligning with our previous quasi-steady-state analyses. Our results generalize earlier mathematical findings, demonstrating that coarsening is driven by self-amplifying mass transport and aggregate coalescence. Additionally, we provide a linear stability analysis of the lateral instability, predicting it through a nullcline-slope criterion that parallels the curvature criterion in spinodal decomposition. Overall, our findings suggest that chemotactic aggregates behave similarly to phase-separating droplets, providing a robust framework for understanding the coarse-grained dynamics of auto-chemotactic cell populations and a quantitative basis for comparing chemotactic coarsening to canonical non-equilibrium phase separation.
24 pages, 6 figures; v2: published version
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