微泡
胶质母细胞瘤
癌症研究
细胞毒性T细胞
免疫疗法
细胞凋亡
程序性细胞死亡
内生
免疫原性细胞死亡
细胞
外体
细胞外小泡
化学
细胞毒性
肿瘤微环境
生物
医学
化疗
细胞存活
癌症免疫疗法
转录组
免疫系统
细胞外
药品
树突状细胞
肿瘤细胞
细胞生物学
小RNA
双重角色
细胞培养
作者
Shiyu Wang,Dongya Zhang,Meng Zheng,Yan Zou,Bingyang Shi
出处
期刊:Nano Letters
[American Chemical Society]
日期:2025-11-24
标识
DOI:10.1021/acs.nanolett.5c04780
摘要
Despite significant therapeutic advances with chemotherapy and immunotherapy in some solid tumors, clinical outcomes for glioblastoma multiform (GBM) remain suboptimal. Owing to their high yield, easy accessibility and cost-effectiveness, plant-derived extracellular vehicles (EVs) have become attractive platforms for biomedical uses. Our study shows that fully natural ginger-derived exosomes (GEXO) effectively inhibited GBM progression through dual mechanisms: (a) direct activation of apoptotic pathways in GBM cells, and (b) induction of immunogenic cell death (ICD) that transforms dead tumor cells into endogenous vaccines. Mechanistically, GEXO demonstrated superior blood-brain barrier (BBB) penetration through clathrin-, caveolin- and macropinocytosis-mediated transcytosis, followed by tumor-specific accumulation via exocytosis. Transcriptomic analysis revealed that GEXO promoted an immunogenic shift in dying GBM cells, enhancing dendritic cell maturation and cytotoxic T-cell responses. In orthotopic GL261 and CT2A models, GEXO significantly prolonged survival without observable toxicity. The natural GEXO platform represents a promising, biosafe strategy with clinical potential for refractory GBM.
科研通智能强力驱动
Strongly Powered by AbleSci AI