上睑下垂
光敏剂
光动力疗法
活性氧
化学
炎症体
癌症研究
癌细胞
细胞凋亡
细胞生物学
癌症
炎症
生物
生物化学
程序性细胞死亡
免疫学
遗传学
有机化学
作者
Min Gao,Qiuting Sun,Huiru Zhang,Mengyu Liu,Rui Peng,Weiji Qin,Qian Wang,Tianhao Yang,Man Zhou,Xiaoyan He,Gengyun Sun
标识
DOI:10.1002/adhm.202401616
摘要
Noninflammatory apoptosis is transformed into inflammatory pyroptosis by activating caspase-3 to lyse gasdermin E (GSDME), and this process can be used as an effective therapeutic strategy. Thus, a selective and powerful inducer of activated caspase-3 plays a vital role in pyroptosis-based cancer therapy. Herein, a human cell membrane vesicle-based nanoplatform (HCNP) is designed for photodynamic therapy (PDT). HCNP is modified with vesicular stomatitis virus G-protein (VSVG) to anchor nano-photosensitizers on the tumor cell membrane. Photosensitizers are bonded to HCNP by clicking chemical reaction as pyroptosis inducers. The results show that HCNP effectively disrupts the mitochondrial function of cells by generating reactive oxygen species (ROS) upon laser irradiation; concomitantly, GSDME is cleaved by activated caspase-3 and promotes pyroptosis of lung cancer cells. Here an effective intervention strategy is proposed to induce pyroptosis based on light-activated PDT.
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