粒体自噬
上睑下垂
线粒体
细胞生物学
材料科学
癌细胞
程序性细胞死亡
纳米技术
生物
细胞凋亡
自噬
生物化学
癌症
遗传学
作者
Yudi Deng,Fuya Jia,Peihang Jiang,Liqiang Chen,Liyun Xing,Xinran Shen,Lian Li,Yuan Huang
出处
期刊:Biomaterials
[Elsevier]
日期:2023-10-01
卷期号:301: 122293-122293
被引量:13
标识
DOI:10.1016/j.biomaterials.2023.122293
摘要
Inducing pyroptosis in cancer cells can result in a strong anti-tumor immune response. Our preliminary study indicates that pyroptosis can be temporarily strengthened by disrupting mitochondria, but ultimately diminished by defensive mitophagy. Here, this study reports a nano-system camouflaged with hybrid membranes consisting of homologous cell membrane and corresponding mitochondrial membrane, which is used to deliver a drug complex Ca@GOx consisting of calcium phosphate and glucose oxidase. By taking advantage of the homing effects of cell membrane and the orientated fusion mechanism of subcellular membrane, the nano-system is able to deliver Ca@GOx to mitochondria, induce mitochondrial Ca2+ overload and generate significant levels of ROS, thus leading to pyroptosis. However, it's found that this system exhibits limited anti-tumor effects in vivo due to the compensatory activation of mitophagy serving as negative feedback to pyroptosis. To address this issue, mitophagy-inhibiting chloroquine is loaded into nanoparticles to intensify pyroptosis. As a result, the combination significantly promotes tumor infiltration of CD8+T cells and improves anti-tumor effects. Together, this study establishes a rational combination of targeted mitochondria disruption and mitophagy blockage for effective pyroptosis-based therapy.
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