自愈水凝胶
细胞外基质
材料科学
透明质酸
组织修复
生物物理学
降级(电信)
脚手架
伤口愈合
组织工程
生物医学工程
细胞外
基质(化学分析)
纳米技术
基底膜
细胞包封
再生(生物学)
膜
组织重塑
微观结构
自愈
化学工程
生物相容性
作者
Zhiyuan Chen,Tuba Marjan,Xinyue Lu,Nicole E. Mertens,Keira Vesy,Dean E. Stornello,James F. Markworth,Taimoor H. Qazi
摘要
Granular hydrogels have attracted widespread interest for wound healing applications, yet their static design, in which microstructure and void space remain fixed, contrasts with the dynamic nature of tissue repair where processes like provisional extracellular matrix (pECM) assembly, cell organization, and nascent tissue formation evolve over time. Here, this disparity is addressed by designing dynamic granular hydrogels that are modularly assembled using microgels with pre-programmed and precise degradation rates ranging from a few days to several weeks. Microgel degradation is controlled via modulation of hydrolytic susceptibility of hyaluronic acid polymers. The biological significance of timed pore expansion in dynamic granular hydrogels is investigated in a mouse muscle crush injury model. While slow-degrading hydrogels support a distinct spatial assembly of cell-instructive interstitial matrix and basement membrane proteins in the expanded pore space, this pECM remodeling is adversely altered in non-degrading or fast-degrading hydrogels. Slow-degrading dynamic granular hydrogels also show long-term therapeutic benefits on muscle wound healing, evidenced by reduced fibrosis, enhanced myogenesis, and improved functional force recovery. Collectively, these striking results demonstrate the profound significance of incorporating dynamicity through controlled microgel degradation in advanced granular biomaterials to improve tissue repair outcomes.
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