Antimicrobial peptides loaded collagen nanosheets with enhanced antibacterial activity, corneal wound healing and M1 macrophage polarization in bacterial keratitis

抗菌剂 角膜炎 巨噬细胞极化 抗菌肽 巨噬细胞 促炎细胞因子 材料科学 体内 抗生素耐药性 抗生素 微生物学 化学 医学 炎症 免疫学 生物 体外 生物化学 生物技术 皮肤病科
作者
Haixiang Huang,Yanyan Xie,Jing Zhong,Zhenyuan Fu,Peimin Wu,Xiaohong Chen,Zhiqiang Xiao,Jin Yuan,Xuetao Shi,Dan Liang
出处
期刊:Composites Part B-engineering [Elsevier BV]
卷期号:275: 111283-111283 被引量:14
标识
DOI:10.1016/j.compositesb.2024.111283
摘要

Bacterial keratitis is one of the leading causes of blindness in the world. Frequent administration of antibiotic eye drops is the first-line treatment, which has difficulties in achieving favorable outcomes in some cases due to the emerging antibiotic resistance and low bioavailability. Antimicrobial peptides have been shown to overcome antibiotic resistance through diverse bactericidal mechanisms including antibiofilm effects, enabling them to be a promising strategy to combat resistance. Here, we report a novel antibacterial strategy with collagen nanosheets (CN) loaded with the cationic antimicrobial short peptide Tet213 (Tet213-CN). In this study, we demonstrated that Tet213-CN possessed excellent properties with good adherence, high oxygen permeability, transparency, biocompatibility, and showed no ocular irritation. In vitro and in vivo assays demonstrated that Tet213-CN had enhanced antibacterial and corneal epithelial healing effects. Furthermore, we observed that Tet213-CN treatment facilitated innate immune defense by promoting M1 macrophage polarization, increasing intracellular ROS generation and proinflammatory cytokine secretion, and enhancing phagocytosis of bacteria via the TLR2/MyD88/NF-κB signaling pathway. Most impressively, Tet213-CN achieved considerable outcomes in Pseudomonas aeruginosa keratitis models with a one-time application. Overall, Tet213-CN may serve as an ideal strategy in the management of bacterial keratitis, and shed new light onto the treatment against antibiotic-resistant bacteria. In addition, these results provide a conceptual framework for a novel macrophage-based strategy in the treatment of corneal infection diseases.
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