Pattern formation along signaling gradients driven by active droplet behavior of cell swarms

Gradients of extracellular signals organize cells in tissues. Although there are several models for how gradients can pattern cell behavior, it is not clear how cells react to gradients when the population is undergoing 3D morphogenesis, in which cell-cell and cell-signal interactions are continually changing. <i>Dictyostelium</i> cells follow gradients of their nutritional source to feed and maintain their undifferentiated state. Using lightsheet imaging to simultaneously monitor signaling, single-cell, and population dynamics, we show that the cells migrate toward nutritional gradients in swarms. As swarms advance, they deposit clumps of cells at the rear, triggering differentiation. Clump deposition is explained by a physical model in which cell swarms behave as active droplets: cells proliferate within the swarm, with clump shedding occurring at a critical population size, at which cells at the rear no longer perceive the gradient and are not retained by the emergent surface tension of the swarm. The model predicts vortex motion of the cells within the swarm emerging from the local transfer of propulsion forces, a prediction validated by 3D tracking of single cells. This active fluid behavior reveals a developmental mechanism we term "musical chairs" decision-making, in which the decision to proliferate or differentiate is determined by the position of a cell within the group as it bifurcates.

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Publication Details

Journal
Proceedings of the National Academy of Sciences
Published
2025-05-20
DOI
https://doi.org/10.1073/pnas.2419152122
Citations
2
Primary Topic
Cellular Mechanics and Interactions
Type
article
Field-Weighted Citation Impact
2.30

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article

Pattern formation along signaling gradients driven by active droplet behavior of cell swarms

Hugh Z. Ford, Jonathan R. Chubb, Mohit P. Dalwadi, Cornelis J. Weijer et al.
2 citations
Proceedings of the National Academy of Sciences
Cellular Mechanics and Interactions
2.30
article

Pattern formation along signaling gradients driven by active droplet behavior of cell swarms

Hugh Z. Ford, Jonathan R. Chubb, Mohit P. Dalwadi, Cornelis J. Weijer, Benjamin J. Walker, Giulia L. Celora, Philip Pearce, Elizabeth R. Westbrook, Hella Baumann
article en
2 citations

Abstract

Gradients of extracellular signals organize cells in tissues. Although there are several models for how gradients can pattern cell behavior, it is not clear how cells react to gradients when the population is undergoing 3D morphogenesis, in which cell-cell and cell-signal interactions are continually changing. <i>Dictyostelium</i> cells follow gradients of their nutritional source to feed and maintain their undifferentiated state. Using lightsheet imaging to simultaneously monitor signaling, single-cell, and population dynamics, we show that the cells migrate toward nutritional gradients in swarms. As swarms advance, they deposit clumps of cells at the rear, triggering differentiation. Clump deposition is explained by a physical model in which cell swarms behave as active droplets: cells proliferate within the swarm, with clump shedding occurring at a critical population size, at which cells at the rear no longer perceive the gradient and are not retained by the emergent surface tension of the swarm. The model predicts vortex motion of the cells within the swarm emerging from the local transfer of propulsion forces, a prediction validated by 3D tracking of single cells. This active fluid behavior reveals a developmental mechanism we term "musical chairs" decision-making, in which the decision to proliferate or differentiate is determined by the position of a cell within the group as it bifurcates.

Proceedings of the National Academy of SciencesVol. 122(21)
University of Dundee (GB), MRC Laboratory for Molecular Cell Biology (GB), University College London (GB), University of Bath (GB)
Wellcome Trust, UK Research and Innovation, Directorate for Biological Sciences, Engineering and Physical Sciences Research Council, Biotechnology and Biological Sciences Research Council
Zero hunger
Openalex Percentile: Top 13%
Cellular Mechanics and Interactions
2.30
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