Suppr超能文献

纳米碱性离子激发的中性粒细胞胞外陷阱消融眼药水促进眼表恢复。

Nano-alkaline ion-excited NETs ablative eye drops promote ocular surface recovery.

作者信息

Zhang Jun, Zhang Lichen, Sun Zhuo, Li Ziang, Zou Xi, Sun Shanshan, Zhu Lin, Xi Kun, Liu Zhinan, Deng Guohua

机构信息

Department of Ophthalmology, Changzhou Third Peopls's Hospital, Changzhou Clinical College of Xuzhou Medical University, 300 Lanlin North road, Changzhou, Jiangsu 213000, China.

Department of Orthopedic Surgery, Orthopedic Institute, The First Affiliated Hospital of Soochow University, 708 Renmin Road, SuZhou, Jiangsu 215000, China.

出版信息

J Control Release. 2025 Feb 10;378:864-879. doi: 10.1016/j.jconrel.2024.12.071. Epub 2024 Dec 31.

Abstract

Neutrophil extracellular traps (NETs) promote neovascularization during the acute phase after ocular chemical injury, while the local inflammatory acidic environment delays post-injury repair. Currently, the mechanism of NETs promoting neovascularization has not been fully elucidated, and there is a lack of therapeutic strategies to effectively improve the local microenvironment for corneal repair. In this study, we validated the NETs-M2-angiogenic pathway after injury. Using transcriptomics sequencing and liquid-phase microarray assays, the intrinsic immune cascade mechanism of NETs inducing macrophage M2 polarization and releasing VEGF via PI3K/AKT was identified. Based on this pathology and the physiological need to improve the local inflammatory acidic environment and promote corneal repair, we organically integrated the alkaline ion-rich bioglass with the highly transmissive and highly adhesive filipin protein, and constructed NETs ablative gel eye drops (DMS) that can release DNase I and alkaline ions in a sustained manner. The eye drops restricted the inflammatory interaction of NETs with macrophages from the source, adhered to the corneal surface and continuously released alkaline ions to improve the local acidic inflammatory environment, providing a favorable immune microenvironment for corneal recovery. We established a cell co-culture system and a corneal alkali burn model to further validate the role of DMS in modulating the intrinsic immune cascade of neovascularization for corneal repair and the related mechanisms. In conclusion, based on the biological mechanism of NETs-M2-VEGF after corneal chemical injury, the present study designed eye drops for dual regulation of intrinsic immunity and the inflammatory acid environment, which not only further supplemented and improved the pathophysiological mechanism of corneal neovascularization after chemical injury, but also provided a new way of thinking about corneal regeneration after injury.

摘要

中性粒细胞胞外陷阱(NETs)在眼部化学伤急性期促进新生血管形成,而局部炎症酸性环境会延迟伤后修复。目前,NETs促进新生血管形成的机制尚未完全阐明,且缺乏有效改善角膜修复局部微环境的治疗策略。在本研究中,我们验证了损伤后NETs-M2-血管生成途径。通过转录组学测序和液相微阵列分析,确定了NETs通过PI3K/AKT诱导巨噬细胞M2极化并释放VEGF的固有免疫级联机制。基于这一病理情况以及改善局部炎症酸性环境和促进角膜修复的生理需求,我们将富碱性离子生物玻璃与高透射性和高黏附性的制霉菌素蛋白有机整合,构建了能持续释放脱氧核糖核酸酶I和碱性离子的NETs消融凝胶滴眼液(DMS)。该滴眼液从源头上限制了NETs与巨噬细胞的炎症相互作用,黏附于角膜表面并持续释放碱性离子以改善局部酸性炎症环境,为角膜恢复提供了有利的免疫微环境。我们建立了细胞共培养系统和角膜碱烧伤模型以进一步验证DMS在调节角膜修复新生血管形成固有免疫级联反应中的作用及相关机制。总之,基于角膜化学伤后NETs-M2-VEGF的生物学机制,本研究设计了用于双重调节固有免疫和炎症酸性环境的滴眼液,不仅进一步补充和完善了化学伤后角膜新生血管形成的病理生理机制,也为伤后角膜再生提供了新的思路。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验