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Crosslinking substrate regulates frictional properties of tissue-engineered cartilage and chondrocyte response to loading

Abstract:
Hydrogels are frequently used in regenerative medicine due to their hydrated, tissue-compatible nature, and tuneable mechanics. While many strategies enable bulk mechanical modulation, little attention is given to tuning surface tribology, and its impact on cellular behavior under mechanical stimuli. Here, we demonstrate that photocrosslinking hydrogels on hydrophobic substrates leads to significant, long-lasting reductions in surface friction, ideal for cartilage tissue regeneration. Gelatin methacryloyl and hyaluronic acid methacrylate hydrogels photocrosslinked on polytetrafluoroethylene possess more hydrated, lubricious surfaces, with lower friction coefficients and crosslinking densities than those crosslinked on glass. This facilitated self-lubrication via water exudation, limiting shear during biaxial stimulation. When subject to intermittent biaxial loading mimicking joint movement, low-friction chondrocyte-laden neo-tissues formed superior hyaline cartilage, confirming the benefits of reduced friction on tissue development. Finally, in situ photocrosslinking enabled precise hydrogel formation in a full-thickness cartilage defect, highlighting the clinical potential and emphasizing the importance of crosslinking substrate in regenerative medicine.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1038/s43246-025-00781-8

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Role:
Author
ORCID:
0000-0002-7036-4067
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Role:
Author
ORCID:
0000-0002-9844-5774
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Role:
Author
ORCID:
0000-0002-9312-7275


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Funder identifier:
https://ror.org/019w4f821
Grant:
660757
Programme:
Horizon 2020 Research and Innovation Programme
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Funder identifier:
https://ror.org/029chgv08
Grant:
098411/Z/12/Z
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Funder identifier:
https://ror.org/05mmh0f86
Programme:
Future Fellowship


Publisher:
Springer Nature
Journal:
Communications Materials More from this journal
Volume:
6
Issue:
1
Article number:
55
Place of publication:
England
Publication date:
2025-03-27
Acceptance date:
2025-03-14
DOI:
EISSN:
2662-4443
Pmid:
40162094


Language:
English
Pubs id:
2102330
Local pid:
pubs:2102330
Deposit date:
2025-05-15
ARK identifier:

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