Department of Respiratory and Critical Care Medicine, The First Affiliated Hospital of Anhui Medical University, Hefei, 230022, China.
School of Life Sciences, Anhui Medical University, Hefei, 230032, China.
Adv Healthc Mater. 2024 Oct;13(26):e2401616. doi: 10.1002/adhm.202401616. Epub 2024 Jun 28.
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.
非炎症性细胞凋亡通过激活半胱氨酸蛋白酶-3(caspase-3)裂解 Gasdermin E(GSDME)转化为炎症性细胞焦亡,该过程可作为一种有效的治疗策略。因此,选择性和有效的激活 caspase-3 诱导剂在基于细胞焦亡的癌症治疗中发挥着重要作用。本文设计了一种基于细胞膜囊泡的纳米平台(HCNP)用于光动力疗法(PDT)。HCNP 通过修饰水疱性口炎病毒 G 蛋白(VSVG)将纳米光敏剂锚定于肿瘤细胞膜上。通过点击化学反应将光敏剂键合到 HCNP 上,作为细胞焦亡的诱导剂。结果表明,HCNP 通过激光照射产生活性氧(ROS)有效破坏细胞的线粒体功能;同时,激活的 caspase-3 裂解 GSDME 并促进肺癌细胞的细胞焦亡。本文提出了一种基于光激活 PDT 的有效干预策略来诱导细胞焦亡。