Researcher profile

Samuel W. S. Johnson

Samuel W. S. Johnson contributes to research discovery and scholarly infrastructure.

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Published work

2 published item(s)

preprint2026arXiv

The spontaneous emergence of leaders and followers in a mathematical model of cranial neural crest cell migration

Many agent-based mathematical models of cranial neural crest cell (CNCC) migration impose a binary phenotypic partition of cells into either leaders or followers. In such models, the movement of leader cells at the front of collectives is guided by local chemoattractant gradients, while follower cells behind leaders move according to local cell-cell guidance cues. Although such model formulations have yielded many insights into the mechanisms underpinning CNCC migration, they rely on fixed phenotypic traits that are difficult to reconcile with evidence of phenotypic plasticity in vivo. A later agent-based model of CNCC migration aimed to address this limitation by allowing cells to adaptively combine chemotactic and cell-cell guidance cues during migration. In this model, cell behaviour adapts instantaneously in response to environmental cues, which precludes the identification of a persistent subset of cells as leader-like over biologically relevant timescales, as observed in vivo. Here, we build on previous leader-follower and adaptive phenotype models to develop a polarity-based agent-based model of CNCC migration, in which all cells evolve according to identical rules, interact via a pairwise interaction potential, and carry polarity vectors that evolve according to a dynamical system driven by time-averaged exposure to chemoattractant gradients. Numerical simulations of this model show that a leader-follower phenotypic partition emerges spontaneously from the underlying collective dynamics of the model. Furthermore, the model reproduces behaviour that is consistent with experimental observations of CNCC migration in the chick embryo. Thus, we provide an experimentally consistent, mechanistically-grounded mathematical model that captures the emergence of leader and follower cell phenotypes without their imposition a priori.

preprint2026arXiv

Theory of adhesion-driven self-organisation in growing tissues

Cell invasion and spatial pattern formation are two distinct manifestations of cellular self-organisation in development, regeneration, and disease. Here, we develop and analyse a unified theoretical framework that links these two seemingly different behaviours within a single mechanistic model for adhesion-mediated self-organisation in growing cell populations. Using a multiscale analysis, we show that the balance between cell-cell adhesion, self-diffusion, and proliferation controls the emergence of distinct collective dynamics. We find that for weak adhesion, tissues invade through stable monotone fronts. As adhesion increases, invasion slows, fronts become unstable, leading to aggregates and spatial patterns emerging behind the advancing edge. In two spatial dimensions, these instabilities generate fingering morphologies reminiscent of dysregulated invasion in cancer. Crucially, we show that density-dependent regulation of adhesion suppresses these instabilities and restores cohesive tissue expansion. Together, our results identify adhesion strength and its regulation as key determinants of whether tissues invade cohesively or fragment into patterns, and provide a unified framework for understanding collective migration, morphogenesis, and dysregulated growth.