Suppr超能文献

仿生纳米光敏剂激活 Caspase-3/GSDME 通路诱导肺癌细胞发生细胞焦亡。

Bioinspired Nano-Photosensitizer-Activated Caspase-3/GSDME Pathway Induces Pyroptosis in Lung Cancer Cells.

机构信息

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.

出版信息

Adv Healthc Mater. 2024 Oct;13(26):e2401616. doi: 10.1002/adhm.202401616. Epub 2024 Jun 28.

Abstract

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.

摘要

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。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验