用双功能肽装饰的透明质酸支架通过抗菌和消炎促进伤口愈合

IF 5.5 2区 化学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Yingzi Wang, Mingda Zhao, Yaping Zou, Xiaojuan Wang, Min Zhang, Yong Sun
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引用次数: 0

摘要

细菌的入侵和炎症阻碍了感染伤口的愈合。在这里,我们设计了一种透明质酸基支架(HAG-g-C),通过与没食子酸修饰的明胶交联来提供蛋白质微环境,并用天然抗菌肽 cathelicidin-BF (CBF) 进行装饰,以清除细菌感染并逆转炎症环境。在体外,HAG-g-C 对金黄色葡萄球菌和大肠杆菌有抗菌作用。同时,它还能促使巨噬细胞的表型从 M1 转为 M2,加速组织重塑。在金黄色葡萄球菌感染的全皮肤缺损小鼠模型中,HAG-g-C能抑制伤口初期的感染过程,并在第12天调节M1巨噬细胞向M2表型转化。此外,HAG-g-C 还能诱导胶原蛋白沉积,减少 TNF-α 的表达,从而显著加快感染伤口的重建。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hyaluronan Scaffold Decorated with Bifunctional Peptide Promotes Wound Healing via Antibacterial and Anti-Inflammatory.

The invasion of bacteria and inflammation impeded infected wounds heal. Here, a hyaluronan-based scaffold (HAG-g-C) was designed by cross-linking with gallic acid-modified gelatin to provide a protein microenvironment and decorated with cathelicidin-BF (CBF), a natural antimicrobial peptide, to remove bacterial infections and reverse the inflammatory environment. In vitro, HAG-g-C presented an antibacterial effect on Staphylococcus aureus and Escherichia coli. Meanwhile, it could drive the phenotypic switch of macrophage from M1 to M2 to accelerate tissue remodeling. In a mouse model of S. aureus-infected total skin defects, HAG-g-C inhibited the process of infection at the beginning of the wound and then regulated the M1 macrophage transformed to M2 phenotype on day 12. In addition, HAG-g-C induced collagen deposition, and reduced the expression of TNF-α, thereby significantly accelerating the reconstruction of infected wounds.

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来源期刊
Biomacromolecules
Biomacromolecules 化学-高分子科学
CiteScore
10.60
自引率
4.80%
发文量
417
审稿时长
1.6 months
期刊介绍: Biomacromolecules is a leading forum for the dissemination of cutting-edge research at the interface of polymer science and biology. Submissions to Biomacromolecules should contain strong elements of innovation in terms of macromolecular design, synthesis and characterization, or in the application of polymer materials to biology and medicine. Topics covered by Biomacromolecules include, but are not exclusively limited to: sustainable polymers, polymers based on natural and renewable resources, degradable polymers, polymer conjugates, polymeric drugs, polymers in biocatalysis, biomacromolecular assembly, biomimetic polymers, polymer-biomineral hybrids, biomimetic-polymer processing, polymer recycling, bioactive polymer surfaces, original polymer design for biomedical applications such as immunotherapy, drug delivery, gene delivery, antimicrobial applications, diagnostic imaging and biosensing, polymers in tissue engineering and regenerative medicine, polymeric scaffolds and hydrogels for cell culture and delivery.
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