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Cooperative effects of Rho and mechanical stretch on stress fiber organization

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What this work says

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

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Rho GTPases control migration and polarization of adhesion molecules and cytoskeletal ERM components in T lymphocytes

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Buckling of actin stress fibers: A new wrinkle in the cytoskeletal tapestry

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Involvement of rho p21 in Cyclic Strain-Induced Tyrosine Phosphorylation of Focal Adhesion Kinase (pp125FAK), Morphological Changes and Migration of Endothelial Cells

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Strain Reorganizes Focal Adhesions and Cytoskeleton in Cultured Airway Smooth Muscle Cells

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Dynamic Reorientation of Cultured Cells and Stress Fibers under Mechanical Stress from Periodic Stretching

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Control of actin dynamics in cell motility

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Substrate Deformation Determines Actin Cytoskeleton Reorganization: A Mathematical Modeling and Experimental Study

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Response of cultured endothelial cells to mechanical stimulation

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The small GTP-binding protein rho regulates the assembly of focal adhesions and actin stress fibers in response to growth factors

inferredcites →https://doi.org/10.1016/0092-8674(94)90259-3openalex-snapshot

The small GTP-binding protein Rho regulates a phosphatidylinositol 4-phosphate 5-kinase in mammalian cells

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Mechanisms of force generation and transmission by myofibroblasts

inferredcites →https://doi.org/10.1016/s0006-3495(02)75280-6openalex-snapshot

Mechanics of F-Actin Characterized with Microfabricated Cantilevers

inferredcites →https://doi.org/10.1016/s0167-4889(97)00100-6openalex-snapshot

Profilins as regulators of actin dynamics

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Cell alignment is induced by cyclic changes in cell length: studies of cells grown in cyclically stretched substrates

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Forces on adhesive contacts affect cell function

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Cooperation between mDia1 and ROCK in Rho-induced actin reorganization

inferredcites →https://doi.org/10.1038/294691a0openalex-snapshot

Are stress fibres contractile?

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Calcium sensitization of smooth muscle mediated by a Rho-associated protein kinase in hypertension

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Pp125FAK is required for stretch dependent morphological response of endothelial cells

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Direct measurement of stiffness of single actin filaments with and without tropomyosin by in vitro nanomanipulation.

inferredcites →https://doi.org/10.1074/jbc.272.48.30455openalex-snapshot

Fluid Shear Stress Activation of Focal Adhesion Kinase

inferredcites →https://doi.org/10.1074/jbc.m107026200openalex-snapshot

mDia-interacting Protein Acts Downstream of Rho-mDia and Modifies Src Activation and Stress Fiber Formation

inferredcites →https://doi.org/10.1083/jcb.102.1.200openalex-snapshot

The molecular organization of myosin in stress fibers of cultured cells.

inferredcites →https://doi.org/10.1083/jcb.133.6.1403openalex-snapshot

Rho-stimulated contractility drives the formation of stress fibers and focal adhesions.

inferredcites →https://doi.org/10.1091/mbc.02-06-0092openalex-snapshot

The Diaphanous-related Formin mDia1 Controls Serum Response Factor Activity through its Effects on Actin Polymerization

inferredcites →https://doi.org/10.1114/1.1317528openalex-snapshot

Contractility Affects Stress Fiber Remodeling and Reorientation of Endothelial Cells Subjected to Cyclic Mechanical Stretching

inferredcites →https://doi.org/10.1114/1.226openalex-snapshot

Measurement of Orientation and Distribution of Cellular Alignment and Cytoskeletal Organization

inferredcites →https://doi.org/10.1114/1.88openalex-snapshot

A Strain Device Imposing Dynamic and Uniform Equi-Biaxial Strain to Cultured Cells

inferredcites →https://doi.org/10.1126/science.275.5304.1308openalex-snapshot

Formation of Actin Stress Fibers and Focal Adhesions Enhanced by Rho-Kinase

inferredcites →https://doi.org/10.1146/annurev.bioeng.6.040803.140040openalex-snapshot

Mechanotransduction at Cell-Matrix and Cell-Cell Contacts

inferredcites →https://doi.org/10.1146/annurev.cb.04.110188.002415openalex-snapshot

Focal Adhesions: Transmembrane Junctions Between the Extracellular Matrix and the Cytoskeleton

inferredcites →https://doi.org/10.1152/ajpcell.00269.2001openalex-snapshot

Cell prestress. I. Stiffness and prestress are closely associated in adherent contractile cells

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Is cytoskeletal tension a major determinant of cell deformability in adherent endothelial cells?

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Involvement of SA channels in orienting response of cultured endothelial cells to cyclic stretch

inferredcites →https://doi.org/10.1152/ajplung.00336.2002openalex-snapshot

Magnitude-dependent regulation of pulmonary endothelial cell barrier function by cyclic stretch

inferredcites →https://doi.org/10.1161/01.hyp.31.1.162openalex-snapshot

Effects of Mechanical Forces on Signal Transduction and Gene Expression in Endothelial Cells

inferredcites →https://doi.org/10.1165/rcmb.4754openalex-snapshot

Mechanical Stress Increases RhoA Activation in Airway Smooth Muscle Cells

inferredcites →https://doi.org/10.1242/jcs.112.9.1365openalex-snapshot

Activation of pp60src is critical for stretch-induced orienting response in fibroblasts

inferredcites →https://doi.org/10.1242/jcs.112.9.1375openalex-snapshot

NH4+-induced down-regulation of the Saccharomyces cerevisiae Gap1p permease involves its ubiquitination with lysine-63-linked chains

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Contractile to extensile transitions and mechanical adaptability enabled by activity in cytoskeletal structures

inferred← citeshttps://doi.org/10.1016/j.ceb.2016.04.011openalex-snapshot

Forces and mechanotransduction in 3D vascular biology

inferred← citeshttps://doi.org/10.1016/j.cellsig.2006.02.008openalex-snapshot

Regulation of stretch-induced JNK activation by stress fiber orientation

inferred← citeshttps://doi.org/10.1016/j.colsurfb.2014.10.031openalex-snapshot

Development of a complex bone tissue culture system based on cellulose nanowhisker mechanical strain

inferred← citeshttps://doi.org/10.1016/j.cossms.2011.04.001openalex-snapshot

Mechanical consequences of cellular force generation

inferred← citeshttps://doi.org/10.1016/j.devcel.2017.08.024openalex-snapshot

Tension Creates an Endoreplication Wavefront that Leads Regeneration of Epicardial Tissue

inferred← citeshttps://doi.org/10.1016/j.eml.2017.12.002openalex-snapshot

Techniques to stimulate and interrogate cell–cell adhesion mechanics

inferred← citeshttps://doi.org/10.1016/j.ijsolstr.2007.06.017openalex-snapshot

Substrate stretching and reorganization of stress fibers as a finite elasticity problem

inferred← citeshttps://doi.org/10.1016/j.ijsolstr.2017.08.023openalex-snapshot

A feedback-loop extended stress fiber growth model with focal adhesion formation

inferred← citeshttps://doi.org/10.1016/j.isci.2026.116279openalex-snapshot

A continuous-discrete model of cell contraction incorporating actin and intermediate filaments

inferred← citeshttps://doi.org/10.1016/j.jbbm.2007.07.005openalex-snapshot

A method to fabricate mesoscopic freestanding polydimethylsiloxane membranes used to probe the rheology of an epithelial sheet

inferred← citeshttps://doi.org/10.1016/j.jbiomech.2006.04.011openalex-snapshot

Molecular basis of the effects of mechanical stretch on vascular smooth muscle cells

inferred← citeshttps://doi.org/10.1016/j.jbiomech.2008.10.014openalex-snapshot

Probing cell structure by controlling the mechanical environment with cell–substrate interactions

inferred← citeshttps://doi.org/10.1016/j.jbiomech.2009.09.012openalex-snapshot

Exogenous and endogenous force regulation of endothelial cell behavior

inferred← citeshttps://doi.org/10.1016/j.jbiomech.2010.05.019openalex-snapshot

Stabilizing to disruptive transition of focal adhesion response to mechanical forces

inferred← citeshttps://doi.org/10.1016/j.jbiomech.2011.06.033openalex-snapshot

Effects of stress fiber contractility on uniaxial stretch guiding mitosis orientation and stress fiber alignment

inferred← citeshttps://doi.org/10.1016/j.jbiomech.2011.10.003openalex-snapshot

An improved texture correlation algorithm to measure substrate–cytoskeletal network strain transfer under large compressive strain

inferred← citeshttps://doi.org/10.1016/j.jbiomech.2011.11.012openalex-snapshot

Dependence of cyclic stretch-induced stress fiber reorientation on stretch waveform

inferred← citeshttps://doi.org/10.1016/j.jbiomech.2013.09.002openalex-snapshot

Tendon extracellular matrix damage detection and quantification using automated edge detection analysis

inferred← citeshttps://doi.org/10.1016/j.jbiomech.2015.10.014openalex-snapshot

The many ways adherent cells respond to applied stretch

inferred← citeshttps://doi.org/10.1016/j.jbiomech.2020.109770openalex-snapshot

As the endothelial cell reorients, its tensile forces stabilize

inferred← citeshttps://doi.org/10.1016/j.jbiomech.2020.109920openalex-snapshot

Role of biomechanics in vascularization of tissue-engineered bones

inferred← citeshttps://doi.org/10.1016/j.jconrel.2021.09.021openalex-snapshot

Mechanical stretching of cells and lipid nanoparticles for nucleic acid delivery

inferred← citeshttps://doi.org/10.1016/j.jiec.2021.04.036openalex-snapshot

Uniaxial stretching device for studying maturity-dependent morphological response of epithelial cell monolayers to tensile strain

inferred← citeshttps://doi.org/10.1016/j.jmbbm.2017.06.006openalex-snapshot

Free energy analysis of cell spreading

inferred← citeshttps://doi.org/10.1016/j.jmbbm.2017.09.018openalex-snapshot

Adaptive responses of murine osteoblasts subjected to coupled mechanical stimuli

inferred← citeshttps://doi.org/10.1016/j.jmbbm.2020.104024openalex-snapshot

Influence of multi-axial dynamic constraint on cell alignment and contractility in engineered tissues

inferred← citeshttps://doi.org/10.1016/j.jmbbm.2026.107564openalex-snapshot

Rotating strain field: Development of a novel mechanical stimulation device and orthogonal alignment of MC3T3-E1 cells in response to anisotropic stimulation

inferred← citeshttps://doi.org/10.1016/j.jmps.2013.08.019openalex-snapshot

Potential-based and non-potential-based cohesive zone formulations under mixed-mode separation and over-closure–Part II: Finite element applications

inferred← citeshttps://doi.org/10.1016/j.jmps.2014.05.016openalex-snapshot

Some basic questions on mechanosensing in cell–substrate interaction

inferred← citeshttps://doi.org/10.1016/j.jmps.2014.07.001openalex-snapshot

On strain and stress in living cells

inferred← citeshttps://doi.org/10.1016/j.jtbi.2008.11.024openalex-snapshot

A kinematic model of stretch-induced stress fiber turnover and reorientation

inferred← citeshttps://doi.org/10.1016/j.jtbi.2009.09.010openalex-snapshot

A multi-scale, discrete-cell simulation of organogenesis: Application to the effects of strain stimulus on collective cell behavior during ameloblast migration

inferred← citeshttps://doi.org/10.1016/j.jtbi.2010.02.020openalex-snapshot

A kinematic model coupling stress fiber dynamics with JNK activation in response to matrix stretching

inferred← citeshttps://doi.org/10.1016/j.jtbi.2023.111564openalex-snapshot

Cell orientation under stretch: A review of experimental findings and mathematical modelling

inferred← citeshttps://doi.org/10.1016/j.matdes.2026.116944openalex-snapshot

A biopolymer-reinforced collagen hydrogel mimicking the 3D mechanical microenvironment promotes osteogenic differentiation via mechanotransduction

inferred← citeshttps://doi.org/10.1016/j.mattod.2025.07.009openalex-snapshot

Advancements in multimodal approaches for enhanced wound healing: From chemical to physical strategies

inferred← citeshttps://doi.org/10.1016/j.mbm.2026.100191openalex-snapshot

Viscous drag-induced self-regeneration of laser-dissected actin stress fibers: A potential mechanism for mechanical memory

inferred← citeshttps://doi.org/10.1016/j.mbs.2013.05.007openalex-snapshot

Regulatory volume decrease of rat kidney principal cells after successive hypo-osmotic shocks

inferred← citeshttps://doi.org/10.1016/j.mechmat.2026.105803openalex-snapshot

A self-consistent mechanobiological theory for active cells in fibrous extracellular matrix

inferred← citeshttps://doi.org/10.1016/j.mtbio.2024.101152openalex-snapshot

Impact of uniaxial cyclic stretching on matrix-associated endothelial cell responses

inferred← citeshttps://doi.org/10.1016/j.plrev.2017.06.016openalex-snapshot

Cellular mechanosensing of the biophysical microenvironment: A review of mathematical models of biophysical regulation of cell responses

inferred← citeshttps://doi.org/10.1016/j.progpolymsci.2016.09.004openalex-snapshot

Dynamically tunable cell culture platforms for tissue engineering and mechanobiology

inferred← citeshttps://doi.org/10.1016/j.snb.2021.129656openalex-snapshot

Stretchable electrical cell-substrate impedance sensor platform for monitoring cell monolayers under strain

inferred← citeshttps://doi.org/10.1016/j.yexcr.2012.05.006openalex-snapshot

CLP36 and RIL recruit α-actinin-1 to stress fibers and differentially regulate stress fiber dynamics in F2408 fibroblasts

inferred← citeshttps://doi.org/10.1016/j.yexcr.2015.07.016openalex-snapshot

The Rho-mDia1 signaling pathway is required for cyclic strain-induced cytoskeletal rearrangement of human periodontal ligament cells

inferred← citeshttps://doi.org/10.1016/j.yexcr.2016.12.002openalex-snapshot

Biomechanics of cell reorientation in a three-dimensional matrix under compression

inferred← citeshttps://doi.org/10.1016/j.yjmcc.2010.02.016openalex-snapshot

Mechanical stress-induced sarcomere assembly for cardiac muscle growth in length and width

inferred← citeshttps://doi.org/10.1016/s0091-679x(10)98007-2openalex-snapshot

Theoretical Concepts and Models of Cellular Mechanosensing

inferred← citeshttps://doi.org/10.1016/s0894-9166(11)60008-6openalex-snapshot

Cell and molecular biomechanics: perspectives and challenges

inferred← citeshttps://doi.org/10.1017/jfm.2013.156openalex-snapshot

Flow of a viscous nematic fluid around a sphere

inferred← citeshttps://doi.org/10.1017/s143192761100002xopenalex-snapshot

A Simplified Implementation of Edge Detection in MATLAB is Faster and More Sensitive than Fast Fourier Transform for Actin Fiber Alignment Quantification

inferred← citeshttps://doi.org/10.1017/s1431927617000666openalex-snapshot

Quantification of Cardiomyocyte Alignment from Three-Dimensional (3D) Confocal Microscopy of Engineered Tissue

inferred← citeshttps://doi.org/10.1021/acs.biomac.8b00992openalex-snapshot

Poly(N-isopropylacrylamide)-Grafted Polydimethylsiloxane Substrate for Controlling Cell Adhesion and Detachment by Dual Stimulation of Temperature and Mechanical Stress

inferred← citeshttps://doi.org/10.1021/acsabm.0c00448openalex-snapshot

Matrix Stiffness Regulates Chemosensitivity, Stemness Characteristics, and Autophagy in Breast Cancer Cells

inferred← citeshttps://doi.org/10.1021/acsami.0c21186openalex-snapshot

Critical Frequency and Critical Stretching Rate for Reorientation of Cells on a Cyclically Stretched Polymer in a Microfluidic Chip

inferred← citeshttps://doi.org/10.1021/acsami.7b04622openalex-snapshot

Parallel Compression Is a Fast Low-Cost Assay for the High-Throughput Screening of Mechanosensory Cytoskeletal Proteins in Cells

inferred← citeshttps://doi.org/10.1021/acsbiomaterials.1c00951openalex-snapshot

Endothelial Cell Migration Regulated by Surface Topography of Poly(ε-caprolactone) Nanofibers

inferred← citeshttps://doi.org/10.1021/acsbiomaterials.8b00628openalex-snapshot

Vascular Endothelial Cell Behavior in Complex Mechanical Microenvironments

inferred← citeshttps://doi.org/10.1021/acsnano.7b01744openalex-snapshot

Gold Nanoparticles Induced Endothelial Leakiness Depends on Particle Size and Endothelial Cell Origin

inferred← citeshttps://doi.org/10.1021/ma401773wopenalex-snapshot

Geometric and Edge Effects on Swelling-Induced Ordered Structure Formation in Polyelectrolyte Hydrogels

inferred← citeshttps://doi.org/10.1038/nature10316openalex-snapshot

Dynamic molecular processes mediate cellular mechanotransduction

inferred← citeshttps://doi.org/10.1038/ncb2693openalex-snapshot

F- and G-actin homeostasis regulates mechanosensitive actin nucleation by formins

inferred← citeshttps://doi.org/10.1038/ncb2917openalex-snapshot

Interplay of RhoA and mechanical forces in collective cell migration driven by leader cells

inferred← citeshttps://doi.org/10.1038/ncomms1668openalex-snapshot

Spatial coordination between cell and nuclear shape within micropatterned endothelial cells

inferred← citeshttps://doi.org/10.1038/ncomms4938openalex-snapshot

Cell reorientation under cyclic stretching

inferred← citeshttps://doi.org/10.1038/ncomms7333openalex-snapshot

Cyclic stretching of soft substrates induces spreading and growth

inferred← citeshttps://doi.org/10.1038/nmat3814openalex-snapshot

Epithelial bridges maintain tissue integrity during collective cell migration

inferred← citeshttps://doi.org/10.1038/nprot.2006.203openalex-snapshot

Micropatterned cell cultures on elastic membranes as an in vitro model of myocardium

inferred← citeshttps://doi.org/10.1038/nrm.2017.101openalex-snapshot

Regulation of genome organization and gene expression by nuclear mechanotransduction

inferred← citeshttps://doi.org/10.1038/nrm3112openalex-snapshot

Balancing forces: architectural control of mechanotransduction

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/s41467-021-24383-3openalex-snapshot

The force loading rate drives cell mechanosensing through both reinforcement and cytoskeletal softening

inferred← citeshttps://doi.org/10.1038/s41467-023-40015-4openalex-snapshot

Engineering tumoral vascular leakiness with gold nanoparticles

inferred← citeshttps://doi.org/10.1038/s41598-021-93987-yopenalex-snapshot

Cyclic stretching-induced epithelial cell reorientation is driven by microtubule-modulated transverse extension during the relaxation phase

inferred← citeshttps://doi.org/10.1038/s41598-023-35675-7openalex-snapshot

Myosin and $$\upalpha$$-actinin regulation of stress fiber contractility under tensile stress

inferred← citeshttps://doi.org/10.1038/s44222-025-00338-xopenalex-snapshot

Bioengineering structural anisotropy in living tissues

inferred← citeshttps://doi.org/10.1038/srep06160openalex-snapshot

Tissue-specific mechanical and geometrical control of cell viability and actin cytoskeleton alignment

inferred← citeshttps://doi.org/10.1038/srep08752openalex-snapshot

Competition between cap and basal actin fiber orientation in cells subjected to contact guidance and cyclic strain

inferred← citeshttps://doi.org/10.1038/srep11620openalex-snapshot

Hypertrophic scar contracture is mediated by the TRPC3 mechanical force transducer via NFkB activation

inferred← citeshttps://doi.org/10.1038/srep35058openalex-snapshot

Regulation of actin catch-slip bonds with a RhoA-formin module

inferred← citeshttps://doi.org/10.1039/9781839165375-00184openalex-snapshot

Engineered Substrates with Dynamically Tunable Topography

inferred← citeshttps://doi.org/10.1039/b703376aopenalex-snapshot

Cell morphology and migration linked to substrate rigidity

inferred← citeshttps://doi.org/10.1039/b806442copenalex-snapshot

Tensegrity-guided self assembly: from molecules to living cells

inferred← citeshttps://doi.org/10.1039/b920644bopenalex-snapshot

A stretching device for imaging real-time molecular dynamics of live cells adhering to elastic membranes on inverted microscopes during the entire process of the stretch

inferred← citeshttps://doi.org/10.1039/c2fd00130fopenalex-snapshot

Cell friction

showing the first 200 of 403

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