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Introduction to cell–hydrogel mechanosensing

Open access
Ahearne, Mark·2014·Interface Focus

Abstract

The development of hydrogel-based biomaterials represents a promising approach to generating new strategies for tissue engineering and regenerative medicine. In order to develop more sophisticated cell-seeded hydrogel constructs, it is important to understand how cells mechanically interact with hydrogels. In this paper, we review the mechanisms by which cells remodel hydrogels, the influence that the hydrogel mechanical and structural properties have on cell behaviour and the role of mechanical stimulation in cell-seeded hydrogels. Cell-mediated remodelling of hydrogels is directed by several cellular processes, including adhesion, migration, contraction, degradation and extracellular matrix deposition. Variations in hydrogel stiffness, density, composition, orientation and viscoelastic characteristics all affect cell activity and phenotype. The application of mechanical force on cells encapsulated in hydrogels can also instigate changes in cell behaviour. By improving our understanding of cell–material mechano-interactions in hydrogels, this should enable a new generation of regenerative medical therapies to be developed.

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Crossref · 10.1098/rsfs.2013.0038

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Metadata

Authors
Ahearne, M.
Venue
Interface Focus
Published
2014-04-06
Volume
4
Issue
2
Pages
20130038-20130038
ISSN
  • 2042-8898 (ISSN-L)
  • 2042-8901
OpenAlex
W2169992315
Cited by
251
References
8
FWCI
5.18
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Introduction to cell–hydrogel mechanosensing. https://app.cochat.ai/papers/10.1098/rsfs.2013.0038
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Ahearne, M. (2014). Introduction to cell–hydrogel mechanosensing. Interface Focus. https://doi.org/10.1098/rsfs.2013.0038

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.