粒体自噬
线粒体
活性氧
声动力疗法
化学
细胞生物学
癌症免疫疗法
免疫原性细胞死亡
免疫检查点
癌症研究
程序性细胞死亡
免疫系统
生物物理学
免疫疗法
细胞凋亡
生物
生物化学
免疫学
自噬
作者
Liping Zuo,Weidong Nie,Songmao Yu,Wan-Ru Zhuang,Chao Liang,Sucheng Li,Danshu Shi,Guanghao Wu,Xin Sui,Yongheng Li,Hai‐Yan Xie
出处
期刊:Nano Letters
[American Chemical Society]
日期:2023-03-29
卷期号:23 (7): 3005-3013
被引量:10
标识
DOI:10.1021/acs.nanolett.3c00383
摘要
Mitochondria are crucial for both sonodynamic therapy and antitumor immunity. However, how to accurately damage mitochondria and meanwhile prevent the mitophagy and immune checkpoint inhibition is still a great challenge. Herein, hexyl 5-aminolevulinate hydrochloride (HAL) and 3-methyladenine (3MA) are loaded into the tumor cell-derived microparticle (X-MP), which can direct the target delivery of the prepared HAL/3MA@X-MP to the tumor cells. HAL induces the confined biosynthesis and accumulation of sonosensitizer PpIX in mitochondria, leading to the localized generation of reactive oxygen species (ROS) upon ultrasound irradiation and, thus, the efficient mitochondrial damage. Meanwhile, 3MA not only inhibits mitophagy but also down-regulates the PD-L1 expression, promoting the immunogenic cell death (ICD) while blocking the immune checkpoint recognition. The smart synergism of precise mitochondrial damage, mitophagy inhibition and antitumor immunity results in potent therapeutic efficacy without obvious side effects.
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