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ForSys: Non-invasive stress inference from time-lapse microscopy
Augusto Borges1,2, Jerónimo R Miranda-Rodríguez1,3, Alberto S Ceccarelli4,5
1Unit Sensory Biology and Organogenesis, Helmholtz Zentrum München, Munich, Germany.
Iscience
|October 29, 2025
Summary
ForSys software estimates cell stresses during tissue development using microscopy. It reveals mechanical forces driving cell behavior and tissue patterns in living organisms.
Area of Science:
- Biophysics
- Developmental Biology
- Computational Biology
Background:
- Mechanical forces are crucial for tissue development and regeneration.
- Measuring these forces in vivo is challenging.
- Existing stress inference algorithms struggle to incorporate tissue dynamics.
Purpose of the Study:
- Introduce ForSys, a novel Python-based software for inferring intercellular stresses and intracellular pressures.
- Enable dynamic stress inference from time-lapse microscopy data.
- Analyze spatiotemporal patterns of mechanical forces during tissue morphogenesis.
Main Methods:
- Developed ForSys, a versatile software tool.
- Validated ForSys using simulated and experimental data.
- Applied ForSys to zebrafish lateral-line primordium migration and neuromast development.
- Integrated ForSys with Fiji for a graphical user interface and accepted segmentation from EPySeg and Cellpose.
Main Results:
- ForSys successfully infers intercellular stresses and intracellular pressures from time-lapse microscopy.
- Revealed increased stress during cell rounding preceding mitosis in zebrafish.
- Accurately predicted the onset of epithelial rosettogenesis.
- Uncovered mechanical asymmetries in neuromast development linked to cell type-specific adhesion.
Conclusions:
- ForSys provides a powerful and versatile tool for analyzing mechanical forces in vivo.
- The software facilitates the study of how mechanical forces regulate tissue morphogenesis and regeneration.
- Enables dynamic stress inference, advancing the field of biophysical analysis in developmental biology.
Keywords:
Optical imaging
