School of Chemistry and Chemical Engineering, Nanchang University, Nanchang 330031, China.
State Key Laboratory of Food Science and Resources, Nanchang University, Nanchang 330047, China.
ACS Nano. 2024 Oct 1;18(39):26666-26689. doi: 10.1021/acsnano.4c05773. Epub 2024 Sep 19.
The biomimetic nanoparticles (NPs) possessing abilities of tumor targeting and multimodal therapy show great potential for efficient combat of colon cancer. Herein, we developed a multifunctional biomimetic nanoplatform (FeO@PDA@CaCO-ICG@CM) based on CaCO-modified magnetic polydopamine (PDA) loaded with indocyanine green (ICG), which was encapsulated by a mouse lymphoma cell (EL4) membrane (CM) expressing functional proteins (i.e., lymphocyte function-associated antigen 1, LFA-1; transforming growth factor-β receptor, TGF-βR; programmed cell death protein 1, PD-1; and factor related apoptosis ligand, FasL). Under magnetic attraction and LFA-1/PD-1-mediated endocytosis, FeO@PDA@CaCO-ICG@CM efficiently targeted CT26 colon tumor cells. The released calcium ion (Ca) from the NPs triggered by acidic tumor microenvironment, the enhanced photothermal effect contributed by the combination of PDA and ICG, and FasL's direct killing effect together induced tumor cells apoptosis. Moreover, the apoptosis of CT26 cells induced immunogenic cell death (ICD) to promote the maturation of dendritic cells (DCs) to activate CD4/CD8 T cells, thereby fighting against tumor cells, which could further be boosted by programmed death-ligand 1 (PD-L1) blockage and transforming growth factor-β (TGF-β) scavenging by FeO@PDA@CaCO-ICG@CM. As a result, satisfactory therapeutic effect was observed for CT26 tumor bearing-mice treated with FeO@PDA@CaCO-ICG@CM under laser irradiation and magnetic attraction, which could eradicate primary tumors and restrain distant tumors through dual tumor targeting-assisted multimodal therapy and eliciting adaptive antitumor immune response, generating the immune memory for inhibiting tumor metastasis and recurrence. Taken together, the multifunctional biomimetic nanoplatform exhibits superior antitumor effects, providing an insightful strategy for the field of nanomaterial-based treatment of cancer.
具有肿瘤靶向和多模式治疗能力的仿生纳米粒子(NPs)在有效对抗结肠癌方面显示出巨大的潜力。在此,我们开发了一种基于 CaCO 修饰的磁性聚多巴胺(PDA)负载吲哚菁绿(ICG)的多功能仿生纳米平台(FeO@PDA@CaCO-ICG@CM),该平台被表达功能蛋白的小鼠淋巴瘤细胞(EL4)膜(CM)包裹,这些蛋白包括淋巴细胞功能相关抗原 1(LFA-1)、转化生长因子-β受体(TGF-βR)、程序性细胞死亡蛋白 1(PD-1)和 FasL。在磁场吸引力和 LFA-1/PD-1 介导的内吞作用下,FeO@PDA@CaCO-ICG@CM 能够有效地靶向 CT26 结肠肿瘤细胞。酸性肿瘤微环境触发 NPs 释放钙离子(Ca),PDA 和 ICG 的协同增强了光热效应,FasL 的直接杀伤作用共同诱导肿瘤细胞凋亡。此外,CT26 细胞的凋亡诱导免疫原性细胞死亡(ICD),促进树突状细胞(DCs)的成熟,激活 CD4/CD8 T 细胞,从而对抗肿瘤细胞,进一步通过程序性死亡配体 1(PD-L1)阻断和 FeO@PDA@CaCO-ICG@CM 对转化生长因子-β(TGF-β)的清除作用来增强。结果,在激光照射和磁场吸引力的作用下,用 FeO@PDA@CaCO-ICG@CM 处理 CT26 荷瘤小鼠表现出令人满意的治疗效果,该治疗能够通过双重肿瘤靶向辅助多模式治疗和引发适应性抗肿瘤免疫反应来根除原发肿瘤并抑制远处肿瘤,从而产生抑制肿瘤转移和复发的免疫记忆。综上所述,多功能仿生纳米平台表现出优异的抗肿瘤效果,为基于纳米材料的癌症治疗领域提供了一种有见地的策略。