自愈水凝胶
生物粘附
脚手架
生物材料
细胞粘附
化学
组织工程
三维细胞培养
焦点粘着
粘附
共焦显微镜
纳米技术
生物物理学
多酚
胶粘剂
生物医学工程
细胞
材料科学
细胞生物学
生物化学
药物输送
高分子化学
有机化学
抗氧化剂
医学
图层(电子)
生物
作者
Di Wu,Jiangtao Zhou,Yang Shen,Cristina Lupo,Qiyao Sun,Tonghui Jin,Shana J. Sturla,Hongshan Liang,Raffaele Mezzenga
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2022-12-22
卷期号:24 (1): 471-480
被引量:9
标识
DOI:10.1021/acs.biomac.2c01311
摘要
Rationally designing microstructures of soft hydrogels for specific biological functionalization is a challenge in tissue engineering applications. A novel and affordable soft hydrogel scaffold is constructed here by incorporating polyphenol modules with lysozyme amyloid fibrils (Lys AFs) via non-covalent self-assembly. Embedded polyphenols not only trigger hydrogel formation but also determine gel behavior by regulating the polyphenol gallol density and complex ratio. The feasibility of using a polyphenol–Lys AF hydrogel as a biocompatible cell scaffold, which is conducive to cell proliferation and spreading, is also shown. Notably, introducing polyphenols imparts the corresponding hydrogels a superior cell bioadhesive efficiency without further biofunctional decoration and thus may be successfully employed in both healthy and cancer cell lines. Confocal laser scanning microscopy also reveals that the highly expressed integrin-mediated focal adhesions form due to stimulation of the polyphenol–AF composite hydrogel, direct cell adhesion, proliferation, and spreading. Overall, this work constitutes a significant step forward in creating highly adhesive tissue culture platforms for in vitro culture of different cell types and may greatly expand prospects for future biomaterial design and development.
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