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Updated: Jul 10, 2025

Control of Cell Adhesion using Hydrogel Patterning Techniques for Applications in Traction Force Microscopy
Published on: January 29, 2022
Patterning and dynamics of membrane adhesion under hydraulic stress
Céline Dinet1,2, Alejandro Torres-Sánchez3,4,5, Roberta Lanfranco6
1Department of Physics, Durham University, Durham, UK.
Pressurized fluid creates tiny cavities (microlumens) at cell connections during development. This study uses lipid vesicles to reveal the physical principles governing microlumen formation and remodeling, offering insights into cell adhesion.
Area of Science:
- Biophysics
- Cell Biology
- Developmental Biology
Background:
- Hydraulic fracturing is crucial for cavity formation in embryonic development, creating lumens from microlumens at cell-cell contacts.
- The underlying physical mechanisms of this process are complex and not fully understood within biological systems.
Purpose of the Study:
- To investigate the physical mechanisms of hydraulic fracturing and microlumen formation using a simplified model system.
- To establish a physical framework for understanding cell-cell adhesion reconfiguration driven by fluid pressure.
Main Methods:
- Experiments using adhered lipid vesicles subjected to osmotic stress to mimic cellular microlumen formation.
- Theoretical modeling and numerical simulations to analyze the physical processes.
- Systematic mapping of microlumen formation conditions, dynamics, and maturation.
Main Results:
- Adhered lipid vesicles form hydraulic microlumens under osmotic stress, similar to biological cells.
- Identified conditions for microlumen formation, observed dynamical patterns, and maturation processes.
- Demonstrated control over hydraulic fracturing by manipulating pressure gradients and membrane bond properties.
Conclusions:
- A physical framework for hydraulic reconfiguration of cell-cell adhesions has been established using lipid vesicles.
- Unexpected passive transition of microlumens to closed buds suggests a physical mechanism for adhesion remodeling via endocytosis.
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