Shape-Morphing Photoresponsive Hydrogels Reveal Dynamic Topographical Conditioning of Fibroblasts

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Samenvatting

The extracellular environment defines a physical boundary condition with which cells interact. However, to date, cell response to geometrical environmental cues is largely studied in static settings, which fails to capture the spatiotemporally varying cues cells receive in native tissues. Here, a photoresponsive spiropyran-based hydrogel is presented as a dynamic, cell-compatible, and reconfigurable substrate. Local stimulation with blue light (455 nm) alters hydrogel swelling, resulting in on-demand reversible micrometer-scale changes in surface topography within 15 min, allowing investigation into cell response to controlled geometry actuations. At short term (1 h after actuation), fibroblasts respond to multiple rounds of recurring topographical changes by reorganizing their nucleus and focal adhesions (FA). FAs form primarily at the dynamic regions of the hydrogel; however, this propensity is abolished when the topography is reconfigured from grooves to pits, demonstrating that topographical changes dynamically condition fibroblasts. Further, this dynamic conditioning is found to be associated with long-term (72 h) maintenance of focal adhesions and epigenetic modifications. Overall, this study offers a new approach to dissect the dynamic interplay between cells and their microenvironment and shines a new light on the cell's ability to adapt to topographical changes through FA-based mechanotransduction.

Originele taal-2Engels
Artikelnummer2303136
Aantal pagina's13
TijdschriftAdvanced Science
Volume10
Nummer van het tijdschrift31
Vroegere onlinedatum23 sep. 2023
DOI's
StatusGepubliceerd - nov. 2023

Financiering

The research project has received financial support from the European Research Council (ERC) under the European Union's Horizon 2020 research and innovation program (CoEvolve, grant no. 851960 for N.A.K. and ForceMorph, grant no. 771168 for C.S.), the Dutch Research Council (OCENW.XS21.4.146 for I.J.), and the Gravitation Program “Materials Driven Regeneration”, funded by the Netherlands Organization for Scientific Research (024.003.013). The authors thank Erwin Dekkers and Patrick de Laat from Equipment and Prototype Center TU/e for their help in designing and manufacturing the illumination device. The authors acknowledge the support from ICMS microscopy facilities under Advanced Analysis focus area. Marc van Maris is acknowledged for his support with the optical profilometry. The authors thank members of the Soft Tissue Engineering and Mechanobiology group for insightful discussions.

FinanciersFinanciernummer
European Research Council
Nederlandse Organisatie voor Wetenschappelijk Onderzoek024.003.013, OCENW.XS21.4.146
Horizon 2020771168, 851960

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