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Biofunctionalized aligned microgels provide 3D cell guidance to mimic complex tissue matrices

Authors :
Christopher Licht
Tamás Haraszti
David B. Gehlen
Jens Köhler
Jonas C. Rose
Laura De Laporte
Source :
Biomaterials, Biomaterials 163, 128-141 (2018). doi:10.1016/j.biomaterials.2018.02.001
Publication Year :
2017

Abstract

Natural healing is based on highly orchestrated processes, in which the extracellular matrix plays a key role. To resemble the native cell environment, we introduce an artificial extracellular matrix (aECM) with the capability to template hierarchical and anisotropic structures in situ, allowing a minimally-invasive application via injection. Synthetic, magnetically responsive, rod-shaped microgels are locally aligned and fixed by a biocompatible surrounding hydrogel, creating a hybrid anisotropic hydrogel (Anisogel), of which the physical, mechanical, and chemical properties can be tailored. The microgels are rendered cell-adhesive with GRGDS and incorporated either inside a cell-adhesive fibrin or bioinert poly(ethylene glycol) hydrogel to strongly interact with fibroblasts. GRGDS-modified microgels inside a fibrin-based Anisogel enhance fibroblast alignment and lead to a reduction in fibronectin production, indicating successful replacement of structural proteins. In addition, YAP-translocation to the nucleus increases with the concentration of microgels, indicating cellular sensing of the overall anisotropic mechanical properties of the Anisogel. For bioinert surrounding PEG hydrogels, GRGDS-microgels are required to support cell proliferation and fibronectin production. In contrast to fibroblasts, primary nerve growth is not significantly affected by the biomodification of the microgels. In conclusion, this approach opens new opportunities towards advanced and complex aECMs for tissue regeneration.

Details

ISSN :
18785905
Volume :
163
Database :
OpenAIRE
Journal :
Biomaterials
Accession number :
edsair.doi.dedup.....9e4d9d2bb7f42c8aa4dc2a4899dce0b8
Full Text :
https://doi.org/10.1016/j.biomaterials.2018.02.001