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Lookup NU author(s): Dr Gema Dura, Dr Maria Crespo Cuadrado, Dr Helen WallerORCiD, Dr Daniel PetersORCiD, Dr Ana Ferreira-DuarteORCiD, Professor Jeremy LakeyORCiD, Dr David Fulton
This is the authors' accepted manuscript of an article that has been published in its final definitive form by Royal Society of Chemistry, 2021.
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Demand continues to grow for biomimetic materials able to create well-defined environments for modulating the behaviour of living cells in culture. Here, we describe hydrogels based upon the polymeric bacterial fimbriae protein capsular antigen fragment 1 (Caf1) that presents tunable biological properties for enhanced tissue cell culture applications. We demonstrate how Caf1 hydrogels can regulate cellular functions such as spreading, proliferation and matrix deposition of human dermal fibroblast cells (hDFBs). Caf1 hydrogels exploring a range of mechanical properties were prepared using copolymers featuring controlled compositions of inert wild-type Caf1 subunits and a mutant subunit displaying the RGDS peptide motif. The hydrogels showed excellent cytocompatibility with hDFBs and the ability to modulate both cell morphology and matrix deposition. Interestingly, Caf1 hydrogels displaying faster stress relaxation were demonstrated to show the highest metabolic activities of growing cells in comparison with other Caf1 hydrogel formulations. The stiffest Caf1 hydrogel impacted cellular morphology, inducing alignment of the cells. This work is significant as it clearly indicates that Caf1-based hydrogels offer tuneable biochemical and mechanical substrates conditions suitable for cell culture applications.
Author(s): Dura G, Crespo-Cuadrado M, Waller H, Peters DT, Ferreira AM, Lakey JH, Fulton DA
Publication type: Article
Publication status: Published
Journal: Biomaterials Science
Year: 2021
Volume: 9
Issue: 7
Pages: 2542-2552
Online publication date: 05/02/2021
Acceptance date: 03/02/2021
Date deposited: 22/04/2021
ISSN (electronic): 2047-4849
Publisher: Royal Society of Chemistry
URL: https://doi.org/10.1039/D0BM01966F
DOI: 10.1039/D0BM01966F
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