透明质酸
内皮
细胞凋亡
渗透(HVAC)
炎症
癌症研究
中性粒细胞胞外陷阱
医学
肺
药理学
肺损伤
化学
脂质体
细胞生物学
内体
免疫学
粒细胞
阿霉素
炎症反应
纳米囊
中性粒细胞
内皮干细胞
免疫疗法
毒品携带者
促炎细胞因子
病理
作者
Jiaxin Li,Yu Hu,Shuang Chen,Yunxia Ye,Yuqian Tang,Wenjing Bai,Nyuk Ling,Haoyuan Luo,Ziyan Dong,Li Min,Ziyi Mo,Sijin Wang,Man Li,Rong Guo,Qin He
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-09-12
卷期号:19 (37): 33372-33386
标识
DOI:10.1021/acsnano.5c09856
摘要
Polymorphonuclear neutrophils (PMNs) are pivotal in acute lung injury (ALI) due to their uncontrollable infiltration and intense inflammatory response. Therefore, we proposed a "cut-off and clean-up" strategy to manipulate PMNs for ALI treatment. To "cut off PMN supply", we consider occupying their binding sites on inflamed endothelium by targeting P-selectin. To precisely "clean up PMNs", we consider specifically inducing their apoptosis and minimizing damage to endothelium and pulmonary parenchyma. Thus, we constructed S-DE/GD, consisting of liposomes containing 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine (DOPE), sulfated hyaluronic acid (SHA) surface modification, and encapsulating glucose-modified doxorubicin (GD). For circulating PMNs, SHA with high P-selectin affinity can inhibit their infiltration. For infiltrated PMNs, the cleanup process involves two steps. First, GD escapes from endosomes utilizing DOPE and is then exocytosed into the lungs through the unidirectional transport of glucose. Subsequently, extruded GD is selectively taken up by infiltrated PMNs overexpressing glucose transporter-1. In ALI mouse model, S-DE/GD demonstrated significant therapeutic efficacy, indicating its potential as a promising strategy for ALI treatment.
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