PLoS ONE · 2009 · 367 citations · 53 references
Tissue EngineeringEngineeringCell AdhesionCytoskeletonMechanotransductionBiomedical EngineeringCellular PhysiologyMost Tissue CellsCell-substrate InteractionsBiomechanicsSparse CulturesMatrix BiologyBiophysicsMechanobiologyNonlinear ElasticityCommunicate Local PositionCell BiomechanicsNon-linear ElasticityFunctional Tissue EngineeringCell EngineeringCell BiologyCell MigrationCell MotilityMedicineExtracellular Matrix
Most tissue cells grown in sparse cultures on linearly elastic substrates typically display a small, round phenotype on soft substrates and become increasingly spread as the modulus of the substrate increases until their spread area reaches a maximum value. As cell density increases, individual cells retain the same stiffness-dependent differences unless they are very close or in molecular contact. On nonlinear strain-stiffening fibrin gels, the same cell types become maximally spread even when the low strain elastic modulus would predict a round morphology, and cells are influenced by the presence of neighbors hundreds of microns away. Time lapse microscopy reveals that fibroblasts and human mesenchymal stem cells on fibrin deform the substrate by several microns up to five cell lengths away from their plasma membrane through a force limited mechanism. Atomic force microscopy and rheology confirm that these strains locally and globally stiffen the gel, depending on cell density, and this effect leads to long distance cell-cell communication and alignment. Thus cells are acutely responsive to the nonlinear elasticity of their substrates and can manipulate this rheological property to induce patterning.
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Matrix Elasticity Directs Stem Cell Lineage Specification
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Tensional homeostasis and the malignant phenotype
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Cell Movement Is Guided by the Rigidity of the Substrate
Chun‐Min Lo, Hong-Bei Wang, Micah Dembo et al. · Biophysical Journal · 2000 · 3.3K citations · Full text
Pattern Formation, Intracellular Transport, Cell Movement Is +12