nir触发的具有H2S和NO生成的可编程纳米马达,用于三级强化ICD级联肿瘤治疗

IF 10.2 1区 医学 Q1 ENGINEERING, BIOMEDICAL Materials Today Bio Pub Date : 2025-04-01 Epub Date: 2025-02-03 DOI:10.1016/j.mtbio.2025.101540
Jinlong Zhang , Quan Jing , Longlong Yuan , Xianhui Zhou , Duolong Di , Jinyao Li , Dong Pei , Zhongxiong Fan , Jun Hai
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引用次数: 0

摘要

气体疗法(GT)和/或光疗最近被用作激活免疫治疗的免疫原性细胞死亡(ICD)药物,然而有效激活足够的免疫反应仍然是这种单一治疗方式的巨大挑战。在这项研究中,一种近红外(NIR)触发的可编程纳米马达,具有硫化氢(H2S)和一氧化氮(NO)的生成,可以通过级联轻度光热、气体和活性氧(ROS)增强的免疫原性细胞死亡来实现肿瘤治疗。简而言之,合成了一种含有H2S和NO的气体信号分子供体NOSH,能够按需释放H2S和NO,然后将其装载到具有固有近红外吸收和表面修饰活性的中空介孔硫化铜纳米粒子(称为HCuSNPs)中,以获得可编程纳米马达(称为NOSH@PEG-HCuSNPs)。特别是NOSH@PEG-HCuSNPs可以有效实现NOSH和HCuSNPs的同时时空共递送,从而发挥GT和轻度光热疗法(mPTT)的协同作用。值得注意的是,GT通过破坏线粒体呼吸链,抑制ATP的产生,促进肿瘤细胞凋亡,有效增强mPTT的抗肿瘤反应。mPTT中的ROS和NOSH中的NO相互作用产生了大量的过氧亚硝酸盐阴离子(ONOO−)自由基。同时,利用H2S独特的保护机制,通过降低热休克蛋白90 (HSP 90)的过表达诱导肿瘤热消融,最大限度地减少对正常组织的不必要损伤。最后,mPTT、ONOO毒血症和H2S的级联效应显著增强了ICD。同时,免疫抑制肿瘤微环境被重新编程,有效抑制远处肿瘤组织,防止肿瘤转移和复发。综上所述,本研究为肿瘤治疗领域的创新提供了新的视角。
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NIR-triggered programmable nanomotor with H2S and NO generation for cascading oncotherapy by three-pronged reinforcing ICD
Gas therapy (GT) and/or phototherapy have been recently employed as immunogenic cell death (ICD) agents for activating immunotherapy, whereas the effective activation of sufficient immune responses remains an enormous challenge in such single therapeutic modality. In this study, a near-infrared (NIR)-triggered programmable nanomotor with hydrogen sulfide (H2S) and nitric oxide (NO) generation is well designed to achieve oncotherapy by cascading mild photothermal, gas, and reactive oxygen species (ROS)-reinforced immunogenic cell death. In brief, a gas signal molecule donor NOSH with H2S and NO capable of on-demand H2S and NO release was synthesized and then loaded into hollow mesoporous copper sulfide nanoparticles (termed as HCuSNPs) with an inherent NIR absorption and surface modification activity to obtain the programmable nanomotor (termed as NOSH@PEG-HCuSNPs). In particular, NOSH@PEG-HCuSNPs can effectively achieve the simultaneous spatiotemporal co-delivery of NOSH and HCuSNPs, thereby exerting the synergistic effects of GT and mild photothermal therapy (mPTT). It is worth noting that the anti-tumor response of mPTT is effectively enhanced by GT by disrupting the mitochondrial respiratory chain, inhibiting ATP production, and promoting tumor cell apoptosis. One by one, a large number of peroxynitrite anion (ONOO) radicals are generated by the interactions of ROS from mPTT and NO from NOSH. Meanwhile, the unique protective mechanism of H2S is utilized to induce tumor thermal ablation by reducing the overexpression of heat shock protein 90 (HSP 90) and minimize the unnecessary damage toward normal tissues. Finally, ICD is markedly augmented by the cascading effects of mPTT, ONOO⁻radicals, and H2S. Concurrently, the immunosuppressive tumor microenvironment is reprogrammed, effectively inhibiting distant tumor tissues and preventing metastasis and tumor recurrence. Taken together, this study provides a new perspective for innovation in the field of oncotherapy.
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来源期刊
CiteScore
8.30
自引率
4.90%
发文量
303
审稿时长
30 days
期刊介绍: Materials Today Bio is a multidisciplinary journal that specializes in the intersection between biology and materials science, chemistry, physics, engineering, and medicine. It covers various aspects such as the design and assembly of new structures, their interaction with biological systems, functionalization, bioimaging, therapies, and diagnostics in healthcare. The journal aims to showcase the most significant advancements and discoveries in this field. As part of the Materials Today family, Materials Today Bio provides rigorous peer review, quick decision-making, and high visibility for authors. It is indexed in Scopus, PubMed Central, Emerging Sources, Citation Index (ESCI), and Directory of Open Access Journals (DOAJ).
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