程序性细胞死亡
溶酶体
溶解循环
化学
脂质双层
脂质过氧化
自噬
药物输送
生物物理学
细胞生物学
活性氧
细胞凋亡
纳米技术
生物化学
抗氧化剂
生物
材料科学
膜
免疫学
酶
病毒
有机化学
作者
Jun Wu,Zhennan Zhao,Hongsheng Wu,Sihuang Lin,Lin Huang,Guanjie Chen,Yi Yang,Hong Wang,Huijie Yan,Shi Yonghui,Liubing Zhu,Guosheng Hu,Liling Zheng,Songying Ouyang
标识
DOI:10.1002/advs.202509208
摘要
Abstract Lipid nanoparticles (LNPs) are recognized as robust and versatile drug delivery platforms holding significant promise for personalized and precision medicine applications. However, their intrinsic biological effects, including dose‐limiting toxicity and acute inflammation, limit their widespread application. Elucidating the underlying mechanisms paradoxically enables dual‐path optimization: targeted mitigation strategies for adverse effects and deliberate amplification of adverse effects for repurposing (“waste‐to‐resource”). Here, cargo‐free lipid nanoparticles containing the ionizable phospholipid IP9 (ipLNP) are found to induce broad swelling (bubble) morphology and lytic cell death across multiple cell types. ipLNP‐induced cell death involves reactive oxygen species (ROS) increase, lipid peroxidation, and GSDME cleavage, but is only inhibited by vitamin E among the tested inhibitors. By exploring the effects of vitamin E, lysosome‐associated lytic cell death is found to be triggered by ipLNP and mediated by lysosome membrane destabilization. Moreover, ipLNP exhibits remarkable potential as novel Th1/Th17‐directing vaccine adjuvants and emerging cancer therapeutic agents, not merely as drug carriers.
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