上睑下垂
程序性细胞死亡
免疫系统
细胞凋亡
细胞生物学
免疫疗法
癌症免疫疗法
癌细胞
细胞
化学
癌症
生物
癌症研究
免疫学
生物化学
遗传学
作者
Pan Zheng,Binbin Ding,Guo‐Qing Zhu,Man Wang,Chunxia Li,Jun Lin
标识
DOI:10.1016/j.cej.2022.137967
摘要
Damage-associated molecular patterns (DAMPs) generated by dying tumor cells can react with host immune systems to activate autonomous immune responses. However, there are still huge challenges in achieving precise release of DAMPs for controllable cancer immunotherapy. As we all know, apoptosis is a process by which cells automatically end their lives determined by genes, and generally does not cause the strong release of DAMPs and immune responses. However, pyroptosis, as an emerging unique pathway of programmed cell death, can trigger a strong inflammatory response by generating large amount of DAMPs. Based on this, we prepared ZnO2 as the donator of H2O2 to trigger pyroptosis and apoptosis by using high concentration of ZnO2 (HZnO2) and low concentration of ZnO2 (LZnO2) respectively, and further compared the different immune activation effects between these two cell death pathways. For the first time, we found HZnO2 can induce pyroptosis effectively and its immune activation effect is better than that of apoptosis induced by LZnO2. Therefore, this nanoplatform provides a new pyroptosis inducer and a new insight for understanding the relationship between cell death pathway and immune responses.
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