可控一体式仿生中空纳米支架,启动热蛋白沉积介导的抗骨肉瘤靶向治疗和骨缺损修复

IF 8.2 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY
Qiming Ma, Shenglin Xu, Qian Wang, Yukang Que, Peng He, Rui Yang, Hao Wang, Ziheng Wu, Longze Xiao, Xingshi Yuan, Xingxing Li, Tangbing Xu, Yong Hu
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引用次数: 0

摘要

热蛋白沉积具有在肿瘤微环境中重振免疫系统的潜力,因而备受关注。然而,目前使用热蛋白沉积诱导剂的方法存在局限性。它们主要依赖单一药物,缺乏精确的靶向性,并可能破坏错综复杂的骨形成微环境,阻碍肿瘤诱导的骨缺损的局部修复。因此,亟需一种既能有效触发热蛋白沉积,又能促进骨再生的治疗策略。本研究介绍了一种旨在解决这些局限性的一体化构建物。它结合了细胞伪装外壳和自增效活性氧(ROS)生成聚合物。该结构包含一个嵌入光敏剂 IR780 的二氧化锰(HMnO2)空心内核,并用 M1 巨噬细胞的细胞膜进行伪装。M1 巨噬细胞膜赋予该构建体隐形特性,使其能够有选择性地聚集在肿瘤部位。在激光照射下,IR780 作为外源触发器产生 ROS,同时将光能转化为热能。此外,HMnO2 的中空结构可作为 IR780 的有效载体。此外,HMnO2 释放出的 Mn4+ 离子会消耗肿瘤内的谷胱甘肽(GSH),进一步扩大 ROS 的产生。这种协同级联反应最终会在激光激活时,通过 Caspase-3 介导的 gasdermin E(GSDME)裂解,诱导热昏迷。同时,HMnO2 在肿瘤微环境(TME)中对 GSH 的消耗导致 Mn2+ 离子的生成。这些 Mn2+ 离子建立了一种支持性环境,可促进骨髓间充质干细胞(BMSCs)转化为成熟的骨细胞。这反过来又促进了大鼠股骨骨缺损的修复。我们的研究结果有力地表明,骨肉瘤的治疗策略可能是热核素沉积,这为骨肉瘤患者的靶向治疗和组织再生提供了一种稳健而多用途的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Controllable All-in-One Biomimetic Hollow Nanoscaffold Initiating Pyroptosis-Mediated Antiosteosarcoma Targeted Therapy and Bone Defect Repair
Pyroptosis has gained attention for its potential to reinvigorate the immune system within the tumor microenvironment. However, current approaches employing pyroptosis inducers suffer from limitations. They primarily rely on single agents, lack precise targeting, and potentially disrupt the intricate bone formation microenvironment, hindering local repair of tumor-induced bone defects. Therefore, a therapeutic strategy is urgently needed that can effectively trigger pyroptosis while simultaneously promoting bone regeneration. This research introduces an all-in-one construct designed to address these limitations. It combines a cell-camouflaged shell with an autosynergistic reactive oxygen species (ROS) generating polymer. This construct incorporates a hollow core of manganese dioxide (HMnO2) embedded with the photosensitizer IR780 and disguised by the cell membrane of an M1 macrophage. The M1 macrophage membrane grants the construct stealth-like properties, enabling it to accumulate selectively at the tumor site. Upon laser irradiation, IR780 acts as an exogenous trigger for ROS generation while simultaneously converting the light energy into heat. Additionally, the hollow structure of HMnO2 serves as an efficient carrier for IR780. Furthermore, Mn4+ ions released from HMnO2 deplete glutathione (GSH) within the tumor, further amplifying ROS production. This synergistic cascade ultimately culminates in pyroptosis induction through caspase-3-mediated cleavage of gasdermin E (GSDME) upon laser activation. Meanwhile, the depletion of GSH by HMnO2 within the tumor microenvironment (TME) leads to the generation of Mn2+ ions. These Mn2+ ions establish a supportive milieu, which promotes the transformation of bone marrow mesenchymal stem cells (BMSCs) into mature bone cells. This, in turn, promotes the repair of bone defects in rat femurs. Our findings strongly indicate that pyroptosis may be a strategy for osteosarcoma treatment, which presents a robust and versatile approach for targeted therapy and tissue regeneration in this patient population.
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来源期刊
ACS Applied Materials & Interfaces
ACS Applied Materials & Interfaces 工程技术-材料科学:综合
CiteScore
16.00
自引率
6.30%
发文量
4978
审稿时长
1.8 months
期刊介绍: ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.
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