线粒体
线粒体DNA
细胞器
化学
细胞生物学
DNA损伤
纳米材料
氧化应激
免疫系统
免疫
癌症研究
生物
DNA
生物化学
纳米技术
材料科学
基因
免疫学
作者
Hao Tian,Wenxi Li,Guohao Wang,Ye Tian,Jie Yan,Xinying Yu,Ziliang Yan,Yuzhao Feng,Yunlu Dai
标识
DOI:10.1002/anie.202411498
摘要
New generation of nanomaterials with organelle‐level precision provide significant promise for targeted attacks on mitochondria, exhibiting remarkable therapeutic potency. Here, we report a novel amphiphilic phenolic polymer (PF) for the mitochondria‐targeted photodynamic therapy (PDT), which can trigger excessive mitochondrial DNA (mtDNA) damages by the synergistic action of oxidative stress and furan‐mediated DNA cross‐linking. Moreover, the phenolic units on PF enable further self‐assembly with Mn2+ via metal‐phenolic coordination to form metal‐phenolic nanomaterial (PFM). We focus on the synergistic activation of the cGAS‐STING pathway by Mn2+ and tumor‐derived mtDNA in tumor‐associated macrophages (TAMs), and subsequently repolarizing M2‐like TAMs to M1 phenotype. We highlight that PFM facilitates the cGAS‐STING‐dependent immunity at the organelle level for potent antitumor efficacy.
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