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Spatiotemporal Oscillation in Confined Epithelial Motion upon Fluid-to-Solid Transition
Jing Yu1, Pingqiang Cai1, Xiaoqian Zhang1
1Innovative Center for Flexible Devices (iFLEX), Max Planck-NTU Joint Lab for Artificial Senses, School of Materials Science and Engineering, Nanyang Technological University, 50 Nanyang Avenue, Singapore 639798, Singapore.
Geometrically confined Madin-Darby canine kidney (MDCK) cell monolayers transition from fluid to solid states. This transition, driven by confinement size-dependent surface tension, regulates cellular mechanics and tissue morphogenesis.
Area of Science:
- Cellular and Tissue Mechanics
- Developmental Biology
- Biophysics
Background:
- Fluid-to-solid phase transitions are vital in multicellular development (e.g., embryogenesis, morphogenesis).
- Biomechanical studies on these transitions are limited, with unknown regulatory factors and cell behavior mechanisms.
- Cellular behavior varies with tissue stress and confinement.
Purpose of the Study:
- To investigate fluid-to-solid phase transitions in geometrically confined multicellular assemblies.
- To identify factors governing these transitions and their impact on cell behavior.
- To elucidate the role of confinement size in regulating cellular mechanics and tissue morphogenesis.
Main Methods:
- Utilized geometrically confined Madin-Darby canine kidney (MDCK) cell monolayers.
- Observed spatiotemporally oscillatory motions dependent on confinement size and periphery distance.
- Performed nanomechanical mapping to assess epithelial tensional stress and substrate traction forces.
Main Results:
- MDCK monolayers exhibited confinement size-dependent oscillatory motions.
- Epithelial tensional stress and traction forces correlated with confinement size.
- Oscillation patterns and nanomechanics were linked to stress fiber assembly and cell polarization.
Conclusions:
- Confinement size-dependent surface tension regulates actin fiber assembly, cellular force generation, and cell polarization.
- A characteristic confinement size was identified that triggers the fluid-to-solid transition.
- Findings offer insights into geometrical and nanomechanical control of tissue morphogenesis and growth.
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