细胞生物学
免疫系统
体内
血管生成
材料科学
肽
神经干细胞
自愈水凝胶
小胶质细胞
炎症
癌症研究
体外
内皮干细胞
再生(生物学)
新生血管
化学
透明质酸
中枢神经系统
细胞凋亡
生物物理学
细胞
肿瘤微环境
冲程(发动机)
平衡
脂质体
细胞外基质
作者
Lin Gan,Tongtong Xu,Dandan Zheng,Ning Zhu,Sijia Li,Shiyu Deng,Qianyuan Lian,Jixian Wang,Wanlu Li,Zhijun Zhang,Guo‐Yuan Yang,Wenguo Cui,Yaohui Tang,Huitong Ruan
标识
DOI:10.1002/adfm.202519806
摘要
ABSTRACT The vascular hyperinflammatory microenvironment significantly influences the regeneration and repair of central nervous system (CNS) following injury. Training immune behavior of immune cells under stress conditions is crucial for maintaining vascular microenvironment homeostasis and restoring vascular function. In this study, we engineer a novel hyperinflammatory regulatory peptide (mND13) by rational grafting of a DJ‐1‐derived peptide with an MMP‐2 responsive peptide motif. This modified peptide is further conjugated onto hyaluronic acid methacrylate (HAMA) microspheres via photo‐click chemistry and microfluidic technology, generating mND13@HAMA microspheres. This platform induces microglia immuno‐training, inhibits their pro‐inflammatory polarization, thus orchestrating neurovascular niche remodeling and promoting neural recovery through immune‐vascular crosstalk. Both in vitro and in vivo investigations show that these immune‐functionalized peptide microspheres mND13@HAMA drastically decrease endothelial cell apoptosis and the expression of pro‐inflammatory molecules like iNOS, CD86 and IL‐1β in microglia. To further enhance post‐stroke angiogenesis, we co‐deliver VEGF liposomes with mND13@HAMA, which is proven to promote vascular sprouting and growth while inhibiting vascular apoptosis. This combined system markedly reduces brain atrophy volume in stroke mouse, improves neurobehavioral functions, and enhances angiogenesis. In conclusion, this immunomodulatory microsphere, capable of training immune cell behavior, holds significant therapeutic value for treating stroke along with other CNS injuries.
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