Issue 29, 2024

Enhancing cell adhesion in synthetic hydrogels via physical confinement of peptide-functionalized polymer clusters

Abstract

Artificially synthesized poly(ethylene glycol) (PEG)-based hydrogels are extensively utilized as biomaterials for tissue scaffolds and cell culture matrices due to their non-protein adsorbing properties. Although these hydrogels are inherently non-cell-adhesive, advancements in modifying polymer networks with functional peptides have led to PEG hydrogels with diverse functionalities, such as cell adhesion and angiogenesis. However, traditional methods of incorporating additives into hydrogel networks often result in the capping of crosslinking points with heterogeneous substances, potentially impairing mechanical properties and obscuring the causal relationships of biological functions. This study introduces polymer additives designed to resist prolonged elution from hydrogels, providing a novel approach to facilitate cell culture on non-adhesive surfaces. By clustering tetra-branched PEG to form ultra-high molecular weight hyper-branched structures and functionalizing their termini with cell-adhesive peptides, we successfully entrapped these clusters within the hydrogel matrix without compromising mechanical strength. This method has enabled successful cell culture on inherently non-adhesive PEG hydrogel surfaces at high peptide densities, a feat challenging to achieve with conventional means. The approach proposed in this study not only paves the way for new possibilities with polymer additives but also serves as a new design paradigm for cell culturing on non-cell-adhesive hydrogels.

Graphical abstract: Enhancing cell adhesion in synthetic hydrogels via physical confinement of peptide-functionalized polymer clusters

Supplementary files

Article information

Article type
Paper
Submitted
08 apr 2024
Accepted
20 jún 2024
First published
24 jún 2024

J. Mater. Chem. B, 2024,12, 7103-7112

Enhancing cell adhesion in synthetic hydrogels via physical confinement of peptide-functionalized polymer clusters

S. Ishikawa, H. Kamata and T. Sakai, J. Mater. Chem. B, 2024, 12, 7103 DOI: 10.1039/D4TB00761A

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