dc.contributor.author
Le Roux, Anabel-Lise
dc.contributor.author
Venturini, Valeria
dc.contributor.author
Gómez González, Manuel
dc.contributor.author
Beedle, Amy E. M.
dc.contributor.author
Quiroga, Xarxa
dc.contributor.author
Menino, Xavier
dc.contributor.author
Trepat Guixer, Xavier
dc.contributor.author
Roca-Cusachs Soulere, Pere
dc.date.accessioned
2026-04-14T18:54:55Z
dc.date.available
2026-04-14T18:54:55Z
dc.date.issued
2026-04-13T08:01:14Z
dc.date.issued
2026-04-13T08:01:14Z
dc.date.issued
2025-06-13
dc.date.issued
2026-04-13T08:01:14Z
dc.identifier
https://hdl.handle.net/2445/228853
dc.identifier.uri
https://hdl.handle.net/2445/228853
dc.description.abstract
Cells are continuously exposed to mechanical forces in physiological and pathological situations, including a variety of tensile and compressive stresses. There is very active research exploring how cells and tissues respond and adapt to such stresses and how these responses integrate with mechanochemical signaling. This has generated a need for sophisticated tools compatible with standard cell culture protocols and microscopy methods, reproducing physiological stresses in in-vitro studies. This study presents the design, function, and characterization of a stretching device compatible with high-resolution optical and fluorescence microscopy. Numerous stretching devices, either pneumatic- or motor-based, have been developed and used in the field. We present one of these systems in detail, including design guidelines, a variety of applications, and all the tools to fabricate a similar setup. The system is based on a deformable polydimethylsiloxane (PDMS) membrane, stretched equibiaxially upon vacuum application, rendering a homogeneous, reproducible, and controlled sample strain. It provides a variety of tensile stresses, from punctual and immediate stretch to repeated stretch-release cycles of controlled amplitude and frequency. Substrate coating with adhesion proteins allows seeding cells bearing fluorescent reporters in the stretching device and performing live-imaging of these cells upon stretch using high magnification fluorescence microscopes. Compressive stresses can also be applied by letting the sample adapt to stretch and subsequently releasing it or by seeding the sample on a pre-stretched substrate before stretch release. Additional topographical patterning of the PDMS substrate enables imaging of the same sample in different microscopy modes (such as fluorescence and electron microscopy). Polyacrylamide gels can also be attached to the PDMS membrane, resulting in the stretching of cells seeded on substrates of different stiffnesses. Overall, by applying controlled tensile stresses on live samples, this stretching device, coupled with high-quality fluorescence microscopy, can address a large variety of questions in mechanobiology.
dc.format
application/pdf
dc.relation
Reproducció del document publicat a: https://doi.org/10.3791/67520
dc.relation
JoVE. Journal of Visualized Experiments, 2025, vol. 220
dc.relation
https://doi.org/10.3791/67520
dc.rights
info:eu-repo/semantics/openAccess
dc.subject
Estrès (Fisiologia)
dc.subject
Stress (Physiology)
dc.title
Equibiaxial Stretching Device for High Magnification Live-Cell Confocal Fluorescence Microscopy
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion