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. Dictyostelium 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.
Original language | English |
---|---|
Article number | e2419152122 |
Journal | Proceedings of the National Academy of Sciences of the United States of America |
Volume | 122 |
Issue number | 21 |
Early online date | 20 May 2025 |
DOIs | |
Publication status | Published - 27 May 2025 |
Data Availability Statement
Time-lapse 3D images data have been deposited in Biostudies (https://doi.org/10.6019/S-BSST1979) (53). Code for modelling is available at https://github.com/giuliacelora/Dictyostelium-Swarm-Migration (54).Acknowledgements
We are grateful to Shu En Lim, Bobby Ford, Adolfo Saiardi, and Olive Ford for materials, Drs. Barrientos, Brimson, Jones, Alasaadi, Mayor, and Wong for discussions, Tim Rudder for interpretations of cell transport, and Philip Maini and Suraj Shankar for discussions about the model.Funding
Work was supported by Wellcome Discovery Award 226655/Z/22/Z to J.R.C. G.L.C. was supported by an Engineering and Physical Sciences Research Council (EPSRC) Doctoral Prize Fellowship (EP/W524335/1). P.P. was supported by a UK Research and Innovation (UKRI) Future Leaders Fellowship (MR/V022385/1). M.P.D. was supported by the EPSRC [EP/W032317/1]. B.J.W. was supported by the Royal Commission for the Exhibition of 1851. Lightsheet imaging was supported by Biotechnology and Biological Sciences Research Council grant (BB/R000441/1) to C.J.W.
Funders | Funder number |
---|---|
Engineering and Physical Sciences Research Council | EP/W524335/1 , EP/W032317/1 |
UK Research and Innovation | MR/V022385/1 |
Biotechnology and Biological Sciences Research Council | BB/R000441/1 |
Keywords
- active droplet
- chemotaxis
- pattern formation
- signaling gradients
- tissue fluidity
ASJC Scopus subject areas
- General