上睑下垂
细胞生物学
免疫系统
化学
内质网
程序性细胞死亡
活性氧
免疫原性细胞死亡
线粒体
癌症研究
线粒体DNA
细胞凋亡
硫氧还蛋白还原酶
DNA损伤
免疫
生物
肿瘤微环境
自噬
T细胞
免疫疗法
细胞
硫氧还蛋白
细胞毒性
转染
作者
Lin Lv,Jing Shi,Zhenfan Wen,Ying Sun,Zhaoran Wang,Qiong Chen,Wukun Liu
摘要
ABSTRACT Targeting mitochondrial DNA (mtDNA) to induce a highly inflammatory form of cell death, such as pyroptosis, represents a promising yet underexplored therapeutic strategy. In this study, we report a novel cationic Au(III) Schiff base complex ( Au9 ) that selectively accumulates in mitochondria, targets mtDNA, and induces mtDNA damage. Additionally, Au9 inhibits thioredoxin reductase (TrxR) activity, elevates reactive oxygen species (ROS) levels, and triggers endoplasmic reticulum stress (ERS). These combined effects activate the caspase‐3/gasdermin E (GSDME) pathway, leading to pyroptosis. This process is accompanied by the release of damage‐associated molecular patterns (DAMPs), significantly enhancing immunogenic cell death (ICD). Further investigations indicate that Au9 effectively modulates the tumor immune microenvironment by promoting dendritic cells (DCs) maturation and CD4 + /CD8 + T cells activation while reducing the proportion of immunosuppressive regulatory T cells (Tregs). This study provides the first evidence that Au(III) complexes can induce pyroptosis by targeting mtDNA and synergistically enhance antitumor immune responses, offering innovative strategies for developing novel metal‐based immunotherapeutic agents.
科研通智能强力驱动
Strongly Powered by AbleSci AI