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Stress relaxation in epithelial monolayers is controlled by actomyosin

https://doi.org/10.1101/302158
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Continual assembly of desmosomes within stable intercellular contacts of epithelial A-431 cells
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In-Vivo Dynamic Deformation of the Mitral Valve Anterior Leaflet
inferredcites →https://doi.org/10.1016/j.bpj.2013.12.031openalex-snapshot
Determinants of Fluidlike Behavior and Effective Viscosity in Cross-Linked Actin Networks
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Rheology of the Active Cell Cortex in Mitosis
inferredcites →https://doi.org/10.1016/j.ceb.2016.02.012openalex-snapshot
A question of time: tissue adaptation to mechanical forces
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The dynamic mechanical properties of cellularised aggregates
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Deconstructing the Cadherin-Catenin-Actin Complex
inferredcites →https://doi.org/10.1016/j.cell.2013.05.008openalex-snapshot
Forces in Tissue Morphogenesis and Patterning
inferredcites →https://doi.org/10.1016/j.chembiol.2009.10.006openalex-snapshot
Identification and Characterization of a Small Molecule Inhibitor of Formin-Mediated Actin Assembly
inferredcites →https://doi.org/10.1016/j.cub.2016.04.007openalex-snapshot
Mechanoaccumulative Elements of the Mammalian Actin Cytoskeleton
inferredcites →https://doi.org/10.1016/j.cub.2017.09.005openalex-snapshot
Viscoelastic Dissipation Stabilizes Cell Shape Changes during Tissue Morphogenesis
inferredcites →https://doi.org/10.1016/j.jbiomech.2009.09.012openalex-snapshot
Exogenous and endogenous force regulation of endothelial cell behavior
inferredcites →https://doi.org/10.1016/j.jbiomech.2009.09.015openalex-snapshot
Recent advances and new opportunities in lung mechanobiology
inferredcites →https://doi.org/10.1016/j.jbiomech.2011.01.020openalex-snapshot
In vivo dynamic strains of the ovine anterior mitral valve leaflet
inferredcites →https://doi.org/10.1016/j.physrep.2007.03.002openalex-snapshot
Rheological properties of the Eukaryotic cell cytoskeleton
inferredcites →https://doi.org/10.1016/j.tcb.2012.07.001openalex-snapshot
Actin cortex mechanics and cellular morphogenesis
inferredcites →https://doi.org/10.1016/s0006-3495(98)77932-9openalex-snapshot
Viscoelastic Properties of Living Embryonic Tissues: a Quantitative Study
inferredcites →https://doi.org/10.1038/nature05824openalex-snapshot
Universal physical responses to stretch in the living cell
inferredcites →https://doi.org/10.1038/nature06953openalex-snapshot
A two-tiered mechanism for stabilization and immobilization of E-cadherin
inferredcites →https://doi.org/10.1038/nature07522openalex-snapshot
Pulsed contractions of an actin–myosin network drive apical constriction
inferredcites →https://doi.org/10.1038/nature08231openalex-snapshot
Characterization of two classes of small molecule inhibitors of Arp2/3 complex
inferredcites →https://doi.org/10.1038/nature08908openalex-snapshot
Cell mechanics and the cytoskeleton
inferredcites →https://doi.org/10.1038/ncb3136openalex-snapshot
E-cadherin junctions as active mechanical integrators in tissue dynamics
inferredcites →https://doi.org/10.1038/ncb3239openalex-snapshot
Feedback regulation through myosin II confers robustness on RhoA signalling at E-cadherin junctions
inferredcites →https://doi.org/10.1038/ncb3525openalex-snapshot
Actin cortex architecture regulates cell surface tension
inferredcites →https://doi.org/10.1038/ncomms5428openalex-snapshot
Filamin acts as a key regulator in epithelial defence against transformed cells
inferredcites →https://doi.org/10.1038/nmat3517openalex-snapshot
The cytoplasm of living cells behaves as a poroelastic material
inferredcites →https://doi.org/10.1038/nmat4206openalex-snapshot
Hydraulic fracture during epithelial stretching
inferredcites →https://doi.org/10.1038/nmeth.1327openalex-snapshot
Tissue tectonics: morphogenetic strain rates, cell shape change and intercalation
inferredcites →https://doi.org/10.1038/nphys3224openalex-snapshot
Active gel physics
inferredcites →https://doi.org/10.1038/nprot.2013.151openalex-snapshot
Generating suspended cell monolayers for mechanobiological studies
inferredcites →https://doi.org/10.1038/nprot.2015.042openalex-snapshot
Dissecting protein reaction dynamics in living cells by fluorescence recovery after photobleaching
inferredcites →https://doi.org/10.1038/nrg3185openalex-snapshot
Insights into the regulation of protein abundance from proteomic and transcriptomic analyses
inferredcites →https://doi.org/10.1038/nrm1356openalex-snapshot
Working out the strength and flexibility of desmosomes
inferredcites →https://doi.org/10.1039/b901311copenalex-snapshot
Power spectrum of out-of-equilibrium forces in living cells: amplitude and frequency dependence
inferredcites →https://doi.org/10.1039/c2sm26648bopenalex-snapshot
Detachment and fracture of cellular aggregates
inferredcites →https://doi.org/10.1063/1.2202921openalex-snapshot
Microplates-based rheometer for a single living cell
inferredcites →https://doi.org/10.1073/pnas.1213301109openalex-snapshot
Characterizing the mechanics of cultured cell monolayers
inferredcites →https://doi.org/10.1073/pnas.1306020110openalex-snapshot
Measuring the regulation of keratin filament network dynamics
inferredcites →https://doi.org/10.1073/pnas.1313491110openalex-snapshot
Keratins as the main component for the mechanical integrity of keratinocytes
inferredcites →https://doi.org/10.1073/pnas.1418732112openalex-snapshot
Direct laser manipulation reveals the mechanics of cell contacts in vivo
inferredcites →https://doi.org/10.1073/pnas.1616659114openalex-snapshot
Measurement of cortical elasticity in Drosophila melanogaster embryos using ferrofluids
inferredcites →https://doi.org/10.1083/jcb.200602085openalex-snapshot
Reassembly of contractile actin cortex in cell blebs
inferredcites →https://doi.org/10.1083/jcb.200910099openalex-snapshot
Integration of contractile forces during tissue invagination
inferredcites →https://doi.org/10.1083/jcb.201008095openalex-snapshot
Cytoskeleton in motion: the dynamics of keratin intermediate filaments in epithelia
inferredcites →https://doi.org/10.1083/jcb.201304143openalex-snapshot
FSGS3/CD2AP is a barbed-end capping protein that stabilizes actin and strengthens adherens junctions
inferredcites →https://doi.org/10.1088/1478-3975/9/4/046004openalex-snapshot
Contraction of cross-linked actomyosin bundles
inferredcites →https://doi.org/10.1093/bioinformatics/btp168openalex-snapshot
Integrating shotgun proteomics and mRNA expression data to improve protein identification
inferredcites →https://doi.org/10.1097/mcc.0000000000000043openalex-snapshot
Epithelial and endothelial damage induced by mechanical ventilation modes
inferredcites →https://doi.org/10.1098/rsif.2012.0263openalex-snapshot
Mechanical state, material properties and continuous description of an epithelial tissue
inferredcites →https://doi.org/10.1101/cshperspect.a015297openalex-snapshot
Desmosomes: Regulators of Cellular Signaling and Adhesion in Epidermal Health and Disease
inferredcites →https://doi.org/10.1103/physreve.74.021911openalex-snapshot
Power laws in microrheology experiments on living cells: Comparative analysis and modeling
inferredcites →https://doi.org/10.1103/physreve.88.012708openalex-snapshot
Physiology-based model of cell viscoelasticity
inferredcites →https://doi.org/10.1103/physrevlett.116.188101openalex-snapshot
Role of Turnover in Active Stress Generation in a Filament Network
inferredcites →https://doi.org/10.1115/1.1894385openalex-snapshot
In Vitro Dynamic Strain Behavior of the Mitral Valve Posterior Leaflet
inferredcites →https://doi.org/10.1115/1.4001682openalex-snapshot
Mechanics of the Mitral Valve Strut Chordae Insertion Region
inferredcites →https://doi.org/10.1126/science.1225399openalex-snapshot
Adhesion Functions in Cell Sorting by Mechanically Coupling the Cortices of Adhering Cells
inferredcites →https://doi.org/10.1140/epje/e2005-00002-5openalex-snapshot
Generic theory of active polar gels: a paradigm for cytoskeletal dynamics
inferredcites →https://doi.org/10.1146/annurev-matsci-062910-100351openalex-snapshot
Linear and Nonlinear Rheology of Living Cells
inferredcites →https://doi.org/10.1152/ajpcell.2000.279.1.c188openalex-snapshot
Contribution of intermediate filaments to cell stiffness, stiffening, and growth
inferredcites →https://doi.org/10.1152/ajplung.00105.2011openalex-snapshot
What do we know about mechanical strain in lung alveoli?
inferredcites →https://doi.org/10.1152/japplphysiol.00160.2007openalex-snapshot
Alveolar expansion imaged by optical sectioning microscopy
inferredcites →https://doi.org/10.1161/01.atv.7.3.276openalex-snapshot
Micropipette aspiration of cultured bovine aortic endothelial cells exposed to shear stress.
inferredcites →https://doi.org/10.1186/s12915-015-0200-yopenalex-snapshot
Emergent material properties of developing epithelial tissues
inferredcites →https://doi.org/10.1186/s13221-015-0033-zopenalex-snapshot
Mechanical stretch: physiological and pathological implications for human vascular endothelial cells
inferredcites →https://doi.org/10.1242/dev.120.4.901openalex-snapshot
Selective disruption of E-cadherin function in early Xenopus embryos by a dominant negative mutant
inferredcites →https://doi.org/10.1242/jcs.142349openalex-snapshot
Formation of adherens junctions leads to the emergence of a tissue-level tension in epithelial monolayers
inferredcites →https://doi.org/10.1529/biophysj.104.050278openalex-snapshot
Creep Function of a Single Living Cell

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Multiscale nature of cell rearrangement caused by collective cell migration
inferred← citeshttps://doi.org/10.1007/s00249-022-01612-1openalex-snapshot
Marangoni effect and cell spreading
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Friction in soft biological systems and surface self-organization: the role of viscoelasticity
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Multiscale Models Coupling Chemical Signaling and Mechanical Properties for Studying Tissue Growth
inferred← citeshttps://doi.org/10.1016/bs.aams.2022.05.002openalex-snapshot
Viscoelasticity and cell swirling motion
inferred← citeshttps://doi.org/10.1016/j.jbiomech.2020.109898openalex-snapshot
Collective cell migration and residual stress accumulation: Rheological consideration
inferred← citeshttps://doi.org/10.1016/j.semcdb.2018.06.003openalex-snapshot
The devil is in the mesoscale: Mechanical and behavioural heterogeneity in collective cell movement
inferred← citeshttps://doi.org/10.1038/s41563-019-0461-xopenalex-snapshot
Actomyosin controls planarity and folding of epithelia in response to compression
inferred← citeshttps://doi.org/10.1038/s41567-020-01134-7openalex-snapshot
Motility-induced fracture reveals a ductile-to-brittle crossover in a simple animal’s epithelia
inferred← citeshttps://doi.org/10.1088/1361-648x/ab6348openalex-snapshot
The 2020 motile active matter roadmap
inferred← citeshttps://doi.org/10.1088/1478-3975/ab39faopenalex-snapshot
The transmembrane protein fibrocystin/polyductin regulates cell mechanics and cell motility
inferred← citeshttps://doi.org/10.1098/rsos.190920openalex-snapshot
A unified rheological model for cells and cellularised materials
inferred← citeshttps://doi.org/10.1103/physreve.98.052409openalex-snapshot
Mechanical oscillations in biological tissues as a result of delayed rest-length changes
inferred← citeshttps://doi.org/10.53846/goediss-7520openalex-snapshot
Collective Mechanical Behavior of Epithelial Cells - The Impact of Micro-Wounding
inferred← citeshttps://doi.org/10.5821/dissertation-2117-124704openalex-snapshot
A theoretical and computational study of soft adhesion mediated by mobile binders
inferred← citeshttps://doi.org/10.70675/bff552baz9546z4f82z85b1z7352701c451eopenalex-snapshot
Optogenetic interrogation of intercellular propagation of force signals
inferred← citeshttps://doi.org/10.7554/elife.83588openalex-snapshot
Force propagation between epithelial cells depends on active coupling and mechano-structural polarization
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