Protease-degradable electrospun fibrous hydrogels

• Published in: Nature communications Vol. 6; no. 1; p. 6639
• Main Authors: Wade, Ryan J., Bassin, Ethan J., Rodell, Christopher B., Burdick, Jason A.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 23.03.2015; Nature Publishing Group
• Subjects: 59; 631/61/2049; 631/61/54/990; 639/301/923/1027; Absorbable Implants; Animals; Humanities and Social Sciences; Hydrogels - chemical synthesis; Hydrogels - metabolism; In Vitro Techniques; Male; Mice; multidisciplinary; Nanofibers; Peptide Hydrolases - metabolism; Science; Science (multidisciplinary); Tissue Scaffolds
• ISSN: 2041-1723; 2041-1723
• DOI: 10.1038/ncomms7639

Electrospun nanofibres are promising in biomedical applications to replicate features of the natural extracellular matrix (ECM). However, nearly all electrospun scaffolds are either non-degradable or degrade hydrolytically, whereas natural ECM degrades proteolytically, often through matrix metalloproteinases. Here we synthesize reactive macromers that contain protease-cleavable and fluorescent peptides and are able to form both isotropic hydrogels and electrospun fibrous hydrogels through a photoinitiated polymerization. These biomimetic scaffolds are susceptible to protease-mediated cleavage in vitro in a protease dose-dependent manner and in vivo in a subcutaneous mouse model using transdermal fluorescent imaging to monitor degradation. Importantly, materials containing an alternate and non-protease-cleavable peptide sequence are stable in both in vitro and in vivo settings. To illustrate the specificity in degradation, scaffolds with mixed fibre populations support selective fibre degradation based on individual fibre degradability. Overall, this represents a novel biomimetic approach to generate protease-sensitive fibrous scaffolds for biomedical applications. Electrospinning is a useful method of biomaterial fabrication, but a lack of bioactivity in the final construct can limit their application as mimics for biological matrices. Here, the authors fabricate a degradable electrospun scaffold as an in vitro and in vivo mimic of the extracellular matrix.