Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry and Sichuan Province, Sichuan Engineering Laboratory for Plant-Sourced Drug and Sichuan Research Center for Drug Precision Industrial Technology, West China School of Pharmacy, Sichuan University, Chengdu, 610041, China.
Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry and Sichuan Province, Sichuan Engineering Laboratory for Plant-Sourced Drug and Sichuan Research Center for Drug Precision Industrial Technology, West China School of Pharmacy, Sichuan University, Chengdu, 610041, China.
Biomaterials. 2023 Oct;301:122293. doi: 10.1016/j.biomaterials.2023.122293. Epub 2023 Aug 24.
Inducing pyroptosis in cancer cells can result in a strong anti-tumor immune response. Our preliminary study indicates that pyroptosis can be temporarily strengthened by disrupting mitochondria, but ultimately diminished by defensive mitophagy. Here, this study reports a nano-system camouflaged with hybrid membranes consisting of homologous cell membrane and corresponding mitochondrial membrane, which is used to deliver a drug complex Ca@GOx consisting of calcium phosphate and glucose oxidase. By taking advantage of the homing effects of cell membrane and the orientated fusion mechanism of subcellular membrane, the nano-system is able to deliver Ca@GOx to mitochondria, induce mitochondrial Ca overload and generate significant levels of ROS, thus leading to pyroptosis. However, it's found that this system exhibits limited anti-tumor effects in vivo due to the compensatory activation of mitophagy serving as negative feedback to pyroptosis. To address this issue, mitophagy-inhibiting chloroquine is loaded into nanoparticles to intensify pyroptosis. As a result, the combination significantly promotes tumor infiltration of CD8T cells and improves anti-tumor effects. Together, this study establishes a rational combination of targeted mitochondria disruption and mitophagy blockage for effective pyroptosis-based therapy.
诱导癌细胞发生细胞焦亡会引发强烈的抗肿瘤免疫反应。我们的初步研究表明,通过破坏线粒体可以暂时增强细胞焦亡,但最终会被防御性的线粒体自噬所削弱。在这里,本研究报告了一种纳米系统,该系统伪装在由同源细胞膜和相应的线粒体膜组成的混合膜中,用于递送由磷酸钙和葡萄糖氧化酶组成的药物复合物 Ca@GOx。利用细胞膜的归巢效应和亚细胞膜的定向融合机制,该纳米系统能够将 Ca@GOx 递送到线粒体,诱导线粒体钙超载并产生大量的 ROS,从而导致细胞焦亡。然而,研究发现,由于线粒体自噬作为细胞焦亡的负反馈而被代偿性激活,该系统在体内表现出有限的抗肿瘤作用。为了解决这个问题,将抑制线粒体自噬的氯喹装载到纳米颗粒中以增强细胞焦亡。结果表明,这种联合治疗显著促进了 CD8T 细胞浸润肿瘤,并提高了抗肿瘤效果。总之,本研究为基于细胞焦亡的有效治疗建立了靶向线粒体破坏和线粒体自噬阻断的合理联合策略。