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Quantification of Cell Edge Velocities and Traction Forces Reveals Distinct Motility Modules during Cell Spreading

https://doi.org/10.1371/journal.pone.0003735
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What this work says

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

inferredcites →https://doi.org/10.1002/(sici)1097-0029(19981201)43:5<433::aid-jemt9>3.0.co;2-2openalex-snapshot
Chemoattractant-induced lamellipod extension
inferredcites →https://doi.org/10.1002/(sici)1097-0169(1996)33:4<241::aid-cm1>3.0.co;2-copenalex-snapshot
Protrusive activity quantitatively determines the rate and direction of cell locomotion
inferredcites →https://doi.org/10.1007/978-0-387-21606-5openalex-snapshot
The Elements of Statistical Learning
inferredcites →https://doi.org/10.1007/978-0-387-84858-7openalex-snapshot
The Elements of Statistical Learning: Data Mining, Inference, and Prediction
inferredcites →https://doi.org/10.1016/0012-1606(92)90246-dopenalex-snapshot
Motile behavior and protrusive activity of migratory mesoderm cells from the Xenopus gastrula
inferredcites →https://doi.org/10.1016/0014-4827(55)90055-0openalex-snapshot
Mitosis in cultures of newt tissues
inferredcites →https://doi.org/10.1016/j.cell.2004.07.019openalex-snapshot
Lamellipodial Versus Filopodial Mode of the Actin Nanomachinery
inferredcites →https://doi.org/10.1016/j.cell.2006.09.044openalex-snapshot
Force Sensing by Mechanical Extension of the Src Family Kinase Substrate p130Cas
inferredcites →https://doi.org/10.1016/j.cell.2006.12.021openalex-snapshot
Trekking across the Brain: The Journey of Neuronal Migration
inferredcites →https://doi.org/10.1016/j.cell.2006.12.039openalex-snapshot
Lamellipodial Actin Mechanically Links Myosin Activity with Adhesion-Site Formation
inferredcites →https://doi.org/10.1016/j.cell.2007.03.037openalex-snapshot
Opposing Effects of PKCθ and WASp on Symmetry Breaking and Relocation of the Immunological Synapse
inferredcites →https://doi.org/10.1016/j.cub.2004.08.047openalex-snapshot
Animal Development: Crowd Control
inferredcites →https://doi.org/10.1016/j.cub.2007.02.058openalex-snapshot
The Universal Dynamics of Cell Spreading
inferredcites →https://doi.org/10.1016/j.tins.2006.10.001openalex-snapshot
Neurons in motion: same principles for different shapes?
inferredcites →https://doi.org/10.1016/s0006-3495(04)74246-0openalex-snapshot
Nanometer Analysis of Cell Spreading on Matrix-Coated Surfaces Reveals Two Distinct Cell States and STEPs
inferredcites →https://doi.org/10.1016/s0014-4827(54)80090-5openalex-snapshot
Mitosis in cultures of newt tissues
inferredcites →https://doi.org/10.1016/s0092-8674(02)00731-6openalex-snapshot
Antagonism between Ena/VASP Proteins and Actin Filament Capping Regulates Fibroblast Motility
inferredcites →https://doi.org/10.1016/s0092-8674(03)00315-5openalex-snapshot
Switch-of-Function Mutants Based on Morphology Classification of Ras Superfamily Small GTPases
inferredcites →https://doi.org/10.1016/s0092-8674(04)00058-3openalex-snapshot
Periodic Lamellipodial Contractions Correlate with Rearward Actin Waves
inferredcites →https://doi.org/10.1016/s0092-8674(04)00456-8openalex-snapshot
RNA and RNA Binding Proteins Participate in Early Stages of Cell Spreading through Spreading Initiation Centers
inferredcites →https://doi.org/10.1016/s1471-4906(01)01872-5openalex-snapshot
Environmental control of immunological synapse formation and duration
inferredcites →https://doi.org/10.1016/s1535-6108(03)00162-4openalex-snapshot
ERK-MAPK signaling coordinately regulates activity of Rac1 and RhoA for tumor cell motility
inferredcites →https://doi.org/10.1038/13040openalex-snapshot
VASP dynamics during lamellipodia protrusion
inferredcites →https://doi.org/10.1038/317314a0openalex-snapshot
Computational vision and regularization theory
inferredcites →https://doi.org/10.1038/35070009openalex-snapshot
Membrane blebbing during apoptosis results from caspase-mediated activation of ROCK I
inferredcites →https://doi.org/10.1038/35070019openalex-snapshot
Caspase-3-mediated cleavage of ROCK I induces MLC phosphorylation and apoptotic membrane blebbing
inferredcites →https://doi.org/10.1038/352126a0openalex-snapshot
Actin microfilament dynamics in locomoting cells
inferredcites →https://doi.org/10.1038/msb4100007openalex-snapshot
From systems biology to synthetic biology
inferredcites →https://doi.org/10.1038/nature01598openalex-snapshot
The cytoskeleton, cellular motility and the reductionist agenda
inferredcites →https://doi.org/10.1038/nature03550openalex-snapshot
Non-equilibration of hydrostatic pressure in blebbing cells
inferredcites →https://doi.org/10.1038/nature04186openalex-snapshot
VEGFR1-positive haematopoietic bone marrow progenitors initiate the pre-metastatic niche
inferredcites →https://doi.org/10.1038/ncb1019openalex-snapshot
Differing modes of tumour cell invasion have distinct requirements for Rho/ROCK signalling and extracellular proteolysis
inferredcites →https://doi.org/10.1038/ncb1367openalex-snapshot
Myosin II functions in actin-bundle turnover in neuronal growth cones
inferredcites →https://doi.org/10.1038/ncb1765openalex-snapshot
Talin depletion reveals independence of initial cell spreading from integrin activation and traction
inferredcites →https://doi.org/10.1038/nri1647openalex-snapshot
Tuning immune responses: diversity and adaptation of the immunological synapse
inferredcites →https://doi.org/10.1038/sj.cdd.4401236openalex-snapshot
Apoptotic and necrotic blebs in epithelial cells display similar neck diameters but different kinase dependency
inferredcites →https://doi.org/10.1038/sj.onc.1204119openalex-snapshot
Glial tumor cell adhesion is mediated by binding of the FNIII domain of receptor protein tyrosine phosphatase β (RPTPβ) to tenascin C
inferredcites →https://doi.org/10.1056/nejm199909023411006openalex-snapshot
Cutaneous Wound Healing
inferredcites →https://doi.org/10.1073/pnas.0408482102openalex-snapshot
Force mapping in epithelial cell migration
inferredcites →https://doi.org/10.1083/jcb.140.3.627openalex-snapshot
Apoptotic Membrane Blebbing Is Regulated by Myosin Light Chain Phosphorylation
inferredcites →https://doi.org/10.1083/jcb.200204153openalex-snapshot
The relationship between force and focal complex development
inferredcites →https://doi.org/10.1083/jcb.200211061openalex-snapshot
RPTP-α acts as a transducer of mechanical force on αv/β3-integrin–cytoskeleton linkages
inferredcites →https://doi.org/10.1083/jcb.200306172openalex-snapshot
Distinct roles of MLCK and ROCK in the regulation of membrane protrusions and focal adhesion dynamics during cell migration of fibroblasts
inferredcites →https://doi.org/10.1091/mbc.9.7.1863openalex-snapshot
Activation of Rac and Cdc42 by Integrins Mediates Cell Spreading
inferredcites →https://doi.org/10.1098/rstb.1982.0122openalex-snapshot
Spreading and locomotion of tissue cells: factors controlling the distribution of pseudopodia
inferredcites →https://doi.org/10.1103/physreve.74.041903openalex-snapshot
1∕f ruffle oscillations in plasma membranes of amphibian epithelial cells under normal and inverted gravitational orientations
inferredcites →https://doi.org/10.1103/physrevlett.93.108105openalex-snapshot
Dynamic Phase Transitions in Cell Spreading
inferredcites →https://doi.org/10.1103/physrevlett.94.158102openalex-snapshot
Kinetics of Cell Spreading
inferredcites →https://doi.org/10.1103/physrevlett.96.098103openalex-snapshot
Neuronal Growth: A Bistable Stochastic Process
inferredcites →https://doi.org/10.1103/physrevlett.97.038102openalex-snapshot
Lateral Membrane Waves Constitute a Universal Dynamic Pattern of Motile Cells
inferredcites →https://doi.org/10.1103/physrevlett.98.168103openalex-snapshot
Membrane Waves Driven by Actin and Myosin
inferredcites →https://doi.org/10.1111/j.1365-2818.1983.tb04158.xopenalex-snapshot
Total internal reflection fluorescent microscopy
inferredcites →https://doi.org/10.1111/j.1440-169x.1977.00103.xopenalex-snapshot
MOTILITY AND LOCOMOTION OF EMBRYONIC CELLS OF THE MEDAKA, ORYZIAS LATIPES, DURING EARLY DEVELOPMENT
inferredcites →https://doi.org/10.1126/science.280.5369.1614openalex-snapshot
Inhibition of Cell Migration, Spreading, and Focal Adhesions by Tumor Suppressor PTEN
inferredcites →https://doi.org/10.1146/annurev.cellbio.21.122303.120306openalex-snapshot
THE GREAT ESCAPE: When Cancer Cells Hijack the Genes for Chemotaxis and Motility
inferredcites →https://doi.org/10.1152/japplphysiol.01181.2004openalex-snapshot
Force sensing and generation in cell phases: analyses of complex functions
inferredcites →https://doi.org/10.1158/0008-5472.can-06-3714openalex-snapshot
Coordinated Regulation of Pathways for Enhanced Cell Motility and Chemotaxis Is Conserved in Rat and Mouse Mammary Tumors
inferredcites →https://doi.org/10.1242/dev.02728openalex-snapshot
Extrinsic and intrinsic mechanisms directing epithelial cell sheet replacement during Drosophila metamorphosis
inferredcites →https://doi.org/10.1242/jcs.00795openalex-snapshot
Regulation of mechanical interactions between fibroblasts and the substratum by stretch-activated Ca2+ entry
inferredcites →https://doi.org/10.1242/jcs.02835openalex-snapshot
The small GTPase R-Ras regulates organization of actin and drives membrane protrusions through the activity of PLCϵ
inferredcites →https://doi.org/10.1242/jcs.03152openalex-snapshot
Dissection of amoeboid movement into two mechanically distinct modes
inferredcites →https://doi.org/10.1242/jcs.03260openalex-snapshot
The small GTPase R-Ras regulates organization of actin and drives membrane protrusions through the activity of PLCϵ
inferredcites →https://doi.org/10.1242/jcs.19.1.169openalex-snapshot
Circus movement in dissociated embryonic cells of a teleost,Oryzias latipes
inferredcites →https://doi.org/10.1242/jcs.61.1.365openalex-snapshot
Kinetic analysis of cell spreading: I. Theory and modelling of curves
inferredcites →https://doi.org/10.1242/jcs.96.1.171openalex-snapshot
Spreading of trypsinized cells: Cytoskeletal dynamics and energy requirements
inferredcites →https://doi.org/10.1371/journal.pbio.0050233openalex-snapshot
Emergence of Large-Scale Cell Morphology and Movement from Local Actin Filament Growth Dynamics
inferredcites →https://doi.org/10.1529/biophysj.105.070383openalex-snapshot
Morphodynamic Profiling of Protrusion Phenotypes
inferredcites →https://doi.org/10.1529/biophysj.106.084806openalex-snapshot
Nonmuscle Myosin IIA-Dependent Force Inhibits Cell Spreading and Drives F-Actin Flow

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.4452019openalex-extracted
inferred← citeshttps://doi.org/10.1002/advs.202207368openalex-snapshot
Actin Filaments Couple the Protrusive Tips to the Nucleus through the I‐BAR Domain Protein IRSp53 during the Migration of Cells on 1D Fibers
inferred← citeshttps://doi.org/10.1002/bies.201600123openalex-snapshot
Integrin and cadherin clusters: A robust way to organize adhesions for cell mechanics
inferred← citeshttps://doi.org/10.1002/cm.21017openalex-snapshot
A review of models of fluctuating protrusion and retraction patterns at the leading edge of motile cells
inferred← citeshttps://doi.org/10.1002/cm.21895openalex-snapshot
Evaluation of lamin A/C mechanotransduction under different surface topography in LMNA related muscular dystrophy
inferred← citeshttps://doi.org/10.1002/wsbm.1386openalex-snapshot
Systems biology of cellular membranes: a convergence with biophysics
inferred← citeshttps://doi.org/10.1007/8415_2010_22openalex-snapshot
Forces During Cell Adhesion and Spreading: Implications for Cellular Homeostasis
inferred← citeshttps://doi.org/10.1007/s10237-015-0673-1openalex-snapshot
Modeling universal dynamics of cell spreading on elastic substrates
inferred← citeshttps://doi.org/10.1007/s12195-009-0057-7openalex-snapshot
Cell–Matrix De-Adhesion Dynamics Reflect Contractile Mechanics
inferred← citeshttps://doi.org/10.1016/b978-0-12-394308-8.00007-8openalex-snapshot
Role of Major Sperm Protein (MSP) in the Protrusion and Retraction of Ascaris Sperm
inferred← citeshttps://doi.org/10.1016/b978-0-12-397897-4.00002-4openalex-snapshot
Multiscale Modeling of Cell Shape from the Actin Cytoskeleton
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2016.05.013openalex-snapshot
Symmetry breaking in spreading RAT2 fibroblasts requires the MAPK/ERK pathway scaffold RACK1 that integrates FAK, p190A-RhoGAP and ERK2 signaling
inferred← citeshttps://doi.org/10.1016/j.bbrc.2013.12.058openalex-snapshot
Cell adhesion and invasion inhibitory effect of an ovarian cancer targeting peptide selected via phage display in vivo
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2017.08.033openalex-snapshot
Mechanically dynamic PDMS substrates to investigate changing cell environments
inferred← citeshttps://doi.org/10.1016/j.bpj.2010.01.059openalex-snapshot
Mechanisms Controlling Cell Size and Shape during Isotropic Cell Spreading
inferred← citeshttps://doi.org/10.1016/j.bpj.2010.07.031openalex-snapshot
Cell Blebbing and Membrane Area Homeostasis in Spreading and Retracting Cells
inferred← citeshttps://doi.org/10.1016/j.bpj.2010.12.3732openalex-snapshot
Signaling Network Triggers and Membrane Physical Properties Control the Actin Cytoskeleton-Driven Isotropic Phase of Cell Spreading
inferred← citeshttps://doi.org/10.1016/j.bpj.2012.03.005openalex-snapshot
Excitable Actin Dynamics in Lamellipodial Protrusion and Retraction
inferred← citeshttps://doi.org/10.1016/j.bpj.2012.09.016openalex-snapshot
Mathematical Modeling of the Impact of Actin and Keratin Filaments on Keratinocyte Cell Spreading
inferred← citeshttps://doi.org/10.1016/j.bpj.2014.04.051openalex-snapshot
Tensional Homeostasis in Single Fibroblasts
inferred← citeshttps://doi.org/10.1016/j.bpj.2014.10.049openalex-snapshot
Dynamics of Cell Area and Force during Spreading
inferred← citeshttps://doi.org/10.1016/j.bpj.2016.11.009openalex-snapshot
Frustrated Phagocytic Spreading of J774A-1 Macrophages Ends in Myosin II-Dependent Contraction
inferred← citeshttps://doi.org/10.1016/j.bpj.2022.10.016openalex-snapshot
Mechanisms of frustrated phagocytic spreading of human neutrophils on antibody-coated surfaces
inferred← citeshttps://doi.org/10.1016/j.ceb.2009.01.020openalex-snapshot
Force propagation across cells: mechanical coherence of dynamic cytoskeletons
inferred← citeshttps://doi.org/10.1016/j.ceb.2012.08.012openalex-snapshot
Traveling waves in actin dynamics and cell motility
inferred← citeshttps://doi.org/10.1016/j.ceb.2015.09.001openalex-snapshot
The mechanisms of spatial and temporal patterning of cell-edge dynamics
inferred← citeshttps://doi.org/10.1016/j.cell.2011.06.010openalex-snapshot
Life at the Leading Edge
inferred← citeshttps://doi.org/10.1016/j.cell.2013.08.026openalex-snapshot
Decoding Information in Cell Shape
inferred← citeshttps://doi.org/10.1016/j.cellsig.2010.07.011openalex-snapshot
PI3-kinase p110α mediates β1 integrin-induced Akt activation and membrane protrusion during cell attachment and initial spreading
inferred← citeshttps://doi.org/10.1016/j.cjac.2021.10.007openalex-snapshot
Activity tracking isolation of Gelsemium elegans alkaloids and evaluation of their antihuman gastric cancer activity in vivo
inferred← citeshttps://doi.org/10.1016/j.cub.2009.06.053openalex-snapshot
The Shape of Motile Cells
inferred← citeshttps://doi.org/10.1016/j.cub.2009.07.063openalex-snapshot
Domain-Driven Morphogenesis of Cellular Membranes
inferred← citeshttps://doi.org/10.1016/j.cub.2016.11.011openalex-snapshot
Adhesion-Dependent Wave Generation in Crawling Cells
inferred← citeshttps://doi.org/10.1016/j.devcel.2013.11.003openalex-snapshot
FHOD1 Is Needed for Directed Forces and Adhesion Maturation during Cell Spreading and Migration
inferred← citeshttps://doi.org/10.1016/j.jmps.2023.105390openalex-snapshot
A computational model for early cell spreading, migration, and competing taxis
inferred← citeshttps://doi.org/10.1016/j.mehy.2021.110640openalex-snapshot
B cell receptor (BCR) guided mechanotransduction: Critical hypothesis to instruct SARS-CoV-2 specific B cells to trigger proximal signalling and antibody reshaping
inferred← citeshttps://doi.org/10.1016/j.snb.2018.10.023openalex-snapshot
Plasmonic Al nanopyramid array sensor for monitoring the attaching and spreading of cells
inferred← citeshttps://doi.org/10.1017/cbo9781139195874.008openalex-snapshot
Toward a Modular Analysis of Cell Mechanosensing and Mechanotransduction
inferred← citeshttps://doi.org/10.1021/acs.jproteome.7b00034openalex-snapshot
Expanding the Interactome of TES by Exploiting TES Modules with Different Subcellular Localizations
inferred← citeshttps://doi.org/10.1021/acsnano.5b05498openalex-snapshot
Determining the Time Window for Dynamic Nanowire Cell Penetration Processes
inferred← citeshttps://doi.org/10.1021/la302219vopenalex-snapshot
Titanium Dioxide Nanoparticles Disturb the Fibronectin-Mediated Adhesion and Spreading of Pre-osteoblastic Cells
inferred← citeshttps://doi.org/10.1021/nl104378fopenalex-snapshot
Nanolithographic Control of the Spatial Organization of Cellular Adhesion Receptors at the Single-Molecule Level
inferred← citeshttps://doi.org/10.1038/emboj.2011.466openalex-snapshot
A novel GRK2/HDAC6 interaction modulates cell spreading and motility
inferred← citeshttps://doi.org/10.1038/nmat2563openalex-snapshot
Material properties of the cell dictate stress-induced spreading and differentiation in embryonic stem cells
inferred← citeshttps://doi.org/10.1038/nphys1613openalex-snapshot
Optimal matrix rigidity for stress-fibre polarization in stem cells
inferred← citeshttps://doi.org/10.1038/nrm3903openalex-snapshot
Appreciating force and shape — the rise of mechanotransduction in cell biology
inferred← citeshttps://doi.org/10.1038/s41467-020-18825-7openalex-snapshot
Complementary mesoscale dynamics of spectrin and acto-myosin shape membrane territories during mechanoresponse
inferred← citeshttps://doi.org/10.1038/s41467-021-22482-9openalex-snapshot
EpCAM promotes endosomal modulation of the cortical RhoA zone for epithelial organization
inferred← citeshttps://doi.org/10.1038/s41598-023-37776-9openalex-snapshot
Growth factors and mechano-regulated reciprocal crosstalk with extracellular matrix tune the keratocyte–fibroblast/myofibroblast transition
inferred← citeshttps://doi.org/10.1038/s42005-018-0075-7openalex-snapshot
Rotating lamellipodium waves in polarizing cells
inferred← citeshttps://doi.org/10.1039/c0lc00487aopenalex-snapshot
A microfluidic system with optical laser tweezers to study mechanotransduction and focal adhesion recruitment
inferred← citeshttps://doi.org/10.1039/c1sm05191aopenalex-snapshot
Control of initial endothelial spreading by topographic activation of focal adhesion kinase
inferred← citeshttps://doi.org/10.1039/c2ib00158fopenalex-snapshot
Numerically bridging lamellipodial and filopodial activity during cell spreading reveals a potentially novel trigger of focal adhesion maturation
inferred← citeshttps://doi.org/10.1039/c4sm00780hopenalex-snapshot
Active mechanics and dynamics of cell spreading on elastic substrates
inferred← citeshttps://doi.org/10.1039/c5sm01706hopenalex-snapshot
Distinct impacts of substrate elasticity and ligand affinity on traction force evolution
inferred← citeshttps://doi.org/10.1039/c6ib00030dopenalex-snapshot
Local extracellular matrix alignment directs cellular protrusion dynamics and migration through Rac1 and FAK
inferred← citeshttps://doi.org/10.1039/d0sm01911aopenalex-snapshot
Transient mechanical interactions between cells and viscoelastic extracellular matrix
inferred← citeshttps://doi.org/10.1073/pnas.1105845108openalex-snapshot
Temporary increase in plasma membrane tension coordinates the activation of exocytosis and contraction during cell spreading
inferred← citeshttps://doi.org/10.1073/pnas.1220723110openalex-snapshot
Integrin-dependent force transmission to the extracellular matrix by α-actinin triggers adhesion maturation
inferred← citeshttps://doi.org/10.1073/pnas.1411785111openalex-snapshot
Three-dimensional cell body shape dictates the onset of traction force generation and growth of focal adhesions
inferred← citeshttps://doi.org/10.1073/pnas.2011785117openalex-snapshot
Stick–slip model for actin-driven cell protrusions, cell polarization, and crawling
inferred← citeshttps://doi.org/10.1074/jbc.m110.144873openalex-snapshot
Mammalian Tropomodulins Nucleate Actin Polymerization via Their Actin Monomer Binding and Filament Pointed End-capping Activities*
inferred← citeshttps://doi.org/10.1074/jbc.m112.431825openalex-snapshot
ELMO Recruits Actin Cross-linking Family 7 (ACF7) at the Cell Membrane for Microtubule Capture and Stabilization of Cellular Protrusions
inferred← citeshttps://doi.org/10.1074/mcp.m111.015099openalex-snapshot
Cells Lacking β-Actin are Genetically Reprogrammed and Maintain Conditional Migratory Capacity*
inferred← citeshttps://doi.org/10.1080/19336918.2019.1568140openalex-snapshot
Hyaluronan-CD44 interactions mediate contractility and migration in periodontal ligament cells
inferred← citeshttps://doi.org/10.1083/jcb.201205169openalex-snapshot
Cdc42 promotes transendothelial migration of cancer cells through β1 integrin
inferred← citeshttps://doi.org/10.1083/jcb.201611117openalex-snapshot
Membrane tension controls adhesion positioning at the leading edge of cells
inferred← citeshttps://doi.org/10.1088/0953-8984/22/19/194106openalex-snapshot
Adhesion patterns in early cell spreading
inferred← citeshttps://doi.org/10.1088/0953-8984/22/19/194110openalex-snapshot
Cell shape, spreading symmetry, and the polarization of stress-fibers in cells
inferred← citeshttps://doi.org/10.1088/1367-2630/14/11/115002openalex-snapshot
Membrane waves driven by forces from actin filaments
inferred← citeshttps://doi.org/10.1088/1478-3975/6/2/025010openalex-snapshot
Excitable waves at the margin of the contact area between a cell and a substrate
inferred← citeshttps://doi.org/10.1091/mbc.e09-03-0240openalex-snapshot
Dephosphorylation of Major Sperm Protein (MSP) Fiber Protein 3 by Protein Phosphatase 2A during Cell Body Retraction in the MSP-based Amoeboid Motility ofAscarisSperm
inferred← citeshttps://doi.org/10.1091/mbc.e10-08-0661openalex-snapshot
Filamin depletion blocks endoplasmic spreading and destabilizes force-bearing adhesions
inferred← citeshttps://doi.org/10.1091/mbc.e16-02-0107openalex-snapshot
α-Actinin links extracellular matrix rigidity-sensing contractile units with periodic cell-edge retractions
inferred← citeshttps://doi.org/10.1093/protein/gzw031openalex-snapshot
The integrin–talin complex under force
inferred← citeshttps://doi.org/10.1096/fj.202402159ropenalex-snapshot
c‐Abl Kinase Targets Tight Junction Protein ZO ‐2 in Regulation of Cell Migration and Morphology
inferred← citeshttps://doi.org/10.1098/rsif.2017.0287openalex-snapshot
Effects of dynamic matrix remodelling on en masse migration of fibroblasts on collagen matrices
inferred← citeshttps://doi.org/10.1098/rsta.2010.0069openalex-snapshot
Cytoskeleton reorganization of spreading cells on micro-patterned islands: a functional model
inferred← citeshttps://doi.org/10.1101/2020.04.14.041335openalex-snapshot
Spatio-temporal mapping of mechanical force generated by macrophages during FcγR-dependent phagocytosis reveals adaptation to target stiffness
inferred← citeshttps://doi.org/10.1101/2022.05.20.492840openalex-snapshot
Actin filaments couple the protrusive tips to the nucleus through the I-BAR domain protein IRSp53 for migration of elongated cells on 1D fibers
inferred← citeshttps://doi.org/10.1101/2022.09.28.509519openalex-snapshot
A full computational model of cell motility: Early spreading, cell migration and competing taxis
inferred← citeshttps://doi.org/10.1101/2023.05.31.543156openalex-snapshot
Cell motility modes are selected by the interplay of mechanosensitive adhesion and membrane tension
inferred← citeshttps://doi.org/10.1101/2023.12.19.572346openalex-snapshot
Excitable Rho dynamics drive cell contractions by sequentially inducing ERM protein-mediated actin-membrane attachment and actomyosin contractility
inferred← citeshttps://doi.org/10.1103/physreve.84.061907openalex-snapshot
Mechanochemical model of cell migration on substrates of varying stiffness
inferred← citeshttps://doi.org/10.1103/prxlife.1.023007openalex-snapshot
Interplay Between Mechanosensitive Adhesions and Membrane Tension Regulates Cell Motility
inferred← citeshttps://doi.org/10.1109/cdc.2013.6760022openalex-snapshot
Regularization-based identification for level set equations
inferred← citeshttps://doi.org/10.1109/icacci.2017.8126203openalex-snapshot
Automated image segmentation for detecting cell spreading for metastasizing assessments of cancer development
inferred← citeshttps://doi.org/10.1126/sciadv.adn6858openalex-snapshot
Excitable Rho dynamics control cell shape and motility by sequentially activating ERM proteins and actomyosin contractility
inferred← citeshttps://doi.org/10.1134/s1990519x13010136openalex-snapshot
Microtubules suppress blebbing and stimulate lamella extension in spreading fibroblasts
inferred← citeshttps://doi.org/10.1140/epjp/s13360-021-01433-9openalex-snapshot
Modelling cellular spreading and emergence of motility in the presence of curved membrane proteins and active cytoskeleton forces
inferred← citeshttps://doi.org/10.1146/annurev-cellbio-100818-125227openalex-snapshot
A Tale of Two States: Normal and Transformed, With and Without Rigidity Sensing
inferred← citeshttps://doi.org/10.11606/t.46.2012.tde-10052013-130119openalex-snapshot
Caracterização funcional das isoformas de splicing do gene ADAM23
inferred← citeshttps://doi.org/10.1242/bio.038968openalex-snapshot
Dynamic microtubules drive fibroblast spreading
inferred← citeshttps://doi.org/10.1242/jcs.042127openalex-snapshot
The mechanical integrin cycle
inferred← citeshttps://doi.org/10.1242/jcs.052704openalex-snapshot
Actin machinery and mechanosensitivity in invadopodia, podosomes and focal adhesions
inferred← citeshttps://doi.org/10.1242/jcs.058297openalex-snapshot
Cytoskeletal coherence requires myosin-IIA contractility
inferred← citeshttps://doi.org/10.1247/csf.12020openalex-snapshot
Image Analysis Tools to Quantify Cell Shape and Protein Dynamics near the Leading Edge
inferred← citeshttps://doi.org/10.1371/journal.pcbi.1004076openalex-snapshot
Model-based Traction Force Microscopy Reveals Differential Tension in Cellular Actin Bundles
inferred← citeshttps://doi.org/10.1371/journal.pcbi.1006321openalex-snapshot
Profiling cellular morphodynamics by spatiotemporal spectrum decomposition
inferred← citeshttps://doi.org/10.1371/journal.pcbi.1009937openalex-snapshot
Integrative experimental/computational approach establishes active cellular protrusion as the primary driving force of phagocytic spreading by immune cells
inferred← citeshttps://doi.org/10.1371/journal.pone.0011631openalex-snapshot
Multi-Environment Model Estimation for Motility Analysis of Caenorhabditis elegans
inferred← citeshttps://doi.org/10.1371/journal.pone.0023807openalex-snapshot
High Refractive Index Silicone Gels for Simultaneous Total Internal Reflection Fluorescence and Traction Force Microscopy of Adherent Cells
inferred← citeshttps://doi.org/10.1371/journal.pone.0025534openalex-snapshot
Measurements of Elastic Moduli of Silicone Gel Substrates with a Microfluidic Device
inferred← citeshttps://doi.org/10.1371/journal.pone.0107097openalex-snapshot
Maturation of Filopodia Shaft Adhesions Is Upregulated by Local Cycles of Lamellipodia Advancements and Retractions
inferred← citeshttps://doi.org/10.1371/journal.pone.0117937openalex-snapshot
Compressive Stress Induces Dephosphorylation of the Myosin Regulatory Light Chain via RhoA Phosphorylation by the Adenylyl Cyclase/Protein Kinase A Signaling Pathway
inferred← citeshttps://doi.org/10.1371/journal.pone.0125746openalex-snapshot
Cell Blebbing upon Addition of Cryoprotectants: A Self-Protection Mechanism
inferred← citeshttps://doi.org/10.17513/mjpfi.12524openalex-snapshot
SPREADING MECHANISMS OF CATTLE MESHENYMAL STEM CELL
inferred← citeshttps://doi.org/10.2174/1566524014666140128113952openalex-snapshot
Computational Methods for Analysis of Dynamic Events in Cell Migration
inferred← citeshttps://doi.org/10.2217/rme.11.99openalex-snapshot
Mechanical Control of Stem Cell Differentiation
inferred← citeshttps://doi.org/10.25560/6361openalex-snapshot
High-Resolution Imaging of Natural Killer Cell Immunological Synapses
inferred← citeshttps://doi.org/10.32657/10356/67023openalex-snapshot
The development of crosslinked keratin-alginate sponges as novel biomaterials
inferred← citeshttps://doi.org/10.3389/fcell.2018.00004openalex-snapshot
Dancing Styles of Collective Cell Migration: Image-Based Computational Analysis of JRAB/MICAL-L2
inferred← citeshttps://doi.org/10.3390/biom10081089openalex-snapshot
Quantitative Phase Imaging of Spreading Fibroblasts Identifies the Role of Focal Adhesion Kinase in the Stabilization of the Cell Rear
inferred← citeshttps://doi.org/10.3390/ijms22168594openalex-snapshot
Keratin-Alginate Sponges Support Healing of Partial-Thickness Burns
inferred← citeshttps://doi.org/10.3390/nano14231891openalex-snapshot
Elongated Particles Show a Preferential Uptake in Invasive Cancer Cells
inferred← citeshttps://doi.org/10.3929/ethz-a-007619561openalex-snapshot
Numerical homogenization of subcellular cytoskeletal processes to reveal novel mechanisms of Rho/Rac dependent adhesion
inferred← citeshttps://doi.org/10.4108/eai.3-12-2015.2262451openalex-snapshot
Learning with amoeba aboard the BioBus
inferred← citeshttps://doi.org/10.48550/arxiv.1906.02559openalex-snapshot
Model of lamellipodium initiation during cell spreading
inferred← citeshttps://doi.org/10.53846/goediss-6418openalex-snapshot
Acto-myosin based mechano-sensitivity of cells - comparing human mesenchymal stem cells and differentiated cells
inferred← citeshttps://doi.org/10.5821/dissertation-2117-371540openalex-snapshot
Multiscale clutch models for cell mechanics
inferred← citeshttps://doi.org/10.70675/ef421d4fzf513z4db8z9492z9a251988e232openalex-snapshot
Physical modelling of cell and tissue mechanics applied to single cell spreading, cancerous budding and cell extrusion
inferred← citeshttps://doi.org/10.7916/d8r78n8ropenalex-snapshot
Endosomal membrane dynamics underlying cell spreading: A role for the small GTPase Arf6
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