Author
Listed:
- Zihui Zhao
(Shanghai Jiao Tong University)
- He Li
(Shanghai Jiao Tong University)
- Yisong Yao
(Shanghai Jiao Tong University)
- Yongfeng Zhao
(Soochow University)
- Francesca Serra
(Johns Hopkins University
University of Southern Denmark)
- Kyogo Kawaguchi
(The University of Tokyo
RIKEN Center for Biosystems Dynamics Research
RIKEN Cluster for Pioneering Research
The University of Tokyo)
- Hepeng Zhang
(Shanghai Jiao Tong University
Shanghai Jiao Tong University)
- Masaki Sano
(Shanghai Jiao Tong University
Shanghai Jiao Tong University
The University of Tokyo)
Abstract
Monolayers of confluent elongated cells are frequently considered active nematics, featuring $$\pm \frac{1}{2}$$ ± 1 2 topological defects. In extensile systems, where cells extend further along their long axis, they can accumulate at $$+\frac{1}{2}$$ + 1 2 defects and escape from $$-\frac{1}{2}$$ − 1 2 defects. Nevertheless, collective dynamics surrounding integer defects remain insufficiently understood. We induce diverse + 1 topological defects (asters, spirals, and targets) within neural progenitor cell monolayers using microfabricated patterns. Remarkably, cells migrate toward the cores of all + 1 defects, challenging existing theories and conventional extensile/contractile dichotomy, which predicts escape from highly bent spirals and targets. By combining experiments and a continuum theory derived from a cell-level model, we identify previously overlooked nonlinear active forces driving this unexpected accumulation toward defect cores, providing a unified framework to explain cell behavior across defect types. Our findings establish + 1 defects as probes to uncover key nonlinear features of active nematics, offering a methodology to characterize and classify cell monolayers.
Suggested Citation
Zihui Zhao & He Li & Yisong Yao & Yongfeng Zhao & Francesca Serra & Kyogo Kawaguchi & Hepeng Zhang & Masaki Sano, 2025.
"Integer topological defects offer a methodology to quantify and classify active cell monolayers,"
Nature Communications, Nature, vol. 16(1), pages 1-11, December.
Handle:
RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-57783-w
DOI: 10.1038/s41467-025-57783-w
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