Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/156386
Title: Spatiotemporal oscillation in confined epithelial motion upon fluid-to-solid transition
Authors: Yu, Jing 
Cai, Pingqiang
Zhang, Xiaoqian
Zhao, Tiankai
Liang, Linlin
Zhang, Sulin
Liu, Hong
Chen, Xiaodong
Keywords: Engineering::Materials
Issue Date: 2021
Source: Yu, J., Cai, P., Zhang, X., Zhao, T., Liang, L., Zhang, S., Liu, H. & Chen, X. (2021). Spatiotemporal oscillation in confined epithelial motion upon fluid-to-solid transition. ACS Nano, 15(4), 7618-7627. https://dx.doi.org/10.1021/acsnano.1c01165
Project: NRF-NRFI2017-07
Journal: ACS Nano 
Abstract: Fluid-to-solid phase transition in multicellular assembly is crucial in many developmental biological processes, such as embryogenesis and morphogenesis. However, biomechanical studies in this area are limited, and little is known about factors governing the transition and how cell behaviors are regulated. Due to different stresses present, cells could behave distinctively depending on the nature of tissue. Here we report a fluid-to-solid transition in geometrically confined multicellular assemblies. Under circular confinement, Madin-Darby canine kidney (MDCK) monolayers undergo spatiotemporally oscillatory motions that are strongly dependent on the confinement size and distance from the periphery of the monolayers. Nanomechanical mapping reveals that epithelial tensional stress and traction forces on the substrate are both dependent on confinement size. The oscillation pattern and cellular nanomechanics profile appear well correlated with stress fiber assembly and cell polarization. These experimental observations imply that the confinement size-dependent surface tension regulates actin fiber assembly, cellular force generation, and cell polarization. Our analyses further suggest a characteristic confinement size (approximates to MDCK's natural correlation length) below which surface tension is sufficiently high and triggers a fluid-to-solid transition of the monolayers. Our findings may shed light on the geometrical and nanomechanical control of tissue morphogenesis and growth.
URI: https://hdl.handle.net/10356/156386
ISSN: 1936-086X
DOI: 10.1021/acsnano.1c01165
Rights: This document is the Accepted Manuscript version of a Published Work that appeared in final form in ACS Nano, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acsnano.1c01165.
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:MSE Journal Articles

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