程序性细胞死亡
纳米孔
细胞生物学
化学
等离子体
纳米技术
膜
生物物理学
材料科学
生物
生物化学
物理
细胞凋亡
量子力学
作者
Hao Li,Zihao Wang,Xiaocui Fang,Wenfeng Zeng,Yanlian Yang,Lingtao Jin,Xiuli Wei,Yan Qin,Chen Wang,Wei Liang
出处
期刊:iScience
[Cell Press]
日期:2022-05-30
卷期号:25 (6): 104481-104481
被引量:12
标识
DOI:10.1016/j.isci.2022.104481
摘要
Immunogenic cell death (ICD) in malignant cells can decrease tumor burden and activate antitumor immune response to obtain lasting antitumor immunity, leading to the elimination of distant metastases and prevention of recurrence. Here, we reveal that ppM1 peptide is capable of forming irreparable transmembrane pores on tumor cell membrane, leading to ICD which we name poroptosis. Poroptosis is directly dependent on cell membrane nanopores regardless of the upstream signaling of cell death. ppM1-induced poroptosis was characterized by the sustained release of intracellular LDH. This unique feature is distinct from other well-characterized types of acute necrosis induced by freezing-thawing (F/T) and detergents, which leads to the burst release of intracellular LDH. Our results suggested that steady transmembrane-nanopore-mediated subacute cell death played a vital role in subsequent activated immunity that transforms to an antitumor immune microenvironment. Selectively generating poroptosis in cancer cell could be a promise strategy for cancer therapy.
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