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Open AccessJournal ArticleDOI

Fibroblast Adaptation and Stiffness Matching to Soft Elastic Substrates

TLDR
Within a range of stiffness spanning that of soft tissues, fibroblasts tune their internal stiffness to match that of their substrate, and modulation of cellular stiffness by the rigidity of the environment may be a mechanism used to direct cell migration and wound repair.
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This article is published in Biophysical Journal.The article was published on 2007-12-15 and is currently open access. It has received 999 citations till now. The article focuses on the topics: Stiffness.

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Mechanotransduction: a major regulator of homeostasis and

TL;DR: This review describes mechanotransduction and the theories underlying how forces may be sensed, from the molecular to organism scale, and the major role it has on organism homeostasis.
Journal ArticleDOI

Nucleation of cadherin clusters on cell-cell interfaces

TL;DR: In this paper , the authors studied collective cadherin organization and interactions within cell-cell contact areas, and found the density at which a 'gas-liquid' phase transition occurs, when Cadherin monomers begin to aggregate into dense clusters.
Posted ContentDOI

Cell strain energy costs of active control of contractility

TL;DR: In this article , a theoretical model of active cell contractility was used to show that upregulation of contractility need not be energetically expensive, especially when combined with changes in adhesion and contractile distribution, and a feedback mechanism based on maintenance of strain energy would require an upregulation in contractile pressure on all but the softest substrates.
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Epithelial cells sense local stiffness via Piezo1 mediated cytoskeletal reorganization

TL;DR: In this article , the authors show that epithelial cells respond to substrate stiffening primarily via actin cytoskeleton organization, that requires activation of mechanosensitive Piezo1 channels.
References
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Journal ArticleDOI

Matrix elasticity directs stem cell lineage specification.

TL;DR: Naive mesenchymal stem cells are shown here to specify lineage and commit to phenotypes with extreme sensitivity to tissue-level elasticity, consistent with the elasticity-insensitive commitment of differentiated cell types.
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Tissue Cells Feel and Respond to the Stiffness of Their Substrate

TL;DR: An understanding of how tissue cells—including fibroblasts, myocytes, neurons, and other cell types—sense matrix stiffness is just emerging with quantitative studies of cells adhering to gels with which elasticity can be tuned to approximate that of tissues.
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Tensional homeostasis and the malignant phenotype.

TL;DR: It is found that tumors are rigid because they have a stiff stroma and elevated Rho-dependent cytoskeletal tension that drives focal adhesions, disrupts adherens junctions, perturbs tissue polarity, enhances growth, and hinders lumen formation.
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Cell Movement Is Guided by the Rigidity of the Substrate

TL;DR: It is discovered that changes in tissue rigidity and strain could play an important controlling role in a number of normal and pathological processes involving cell locomotion, including morphogenesis, the immune response, and wound healing.
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Cell locomotion and focal adhesions are regulated by substrate flexibility

TL;DR: The ability of cells to survey the mechanical properties of their surrounding environment is demonstrated and the possible involvement of both protein tyrosine phosphorylation and myosin-generated cortical forces in this process is suggested.
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