胶质瘤干细胞膜包裹的磁响应仿生纳米系统有效靶向和消除恶性胶质瘤。

IF 9.8 Q1 ENGINEERING, BIOMEDICAL Biomaterials research Pub Date : 2024-12-27 eCollection Date: 2024-01-01 DOI:10.34133/bmr.0123
Song Deng, Dekang Nie, Yue Huang, Yu Yang, Qianqian Liu, Zesheng Sun, Qiaoji Jiang, Yuejuan Ling, Ya Wen, Jiahua Qu, Jialiang Lin, Yi Wang, Rongqin Huang, Jinlong Shi
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引用次数: 0

摘要

多形性胶质母细胞瘤(GBM)是最具挑战性的恶性脑肿瘤之一,因此开发新的治疗策略非常必要。胶质瘤干细胞(GSCs)对GBM的耐药、耐辐射和肿瘤复发有显著影响。靶向GSCs的纳米材料治疗GBM的潜力亟待探索。设计了一种磁响应仿生纳米系统(FDPM),该系统包被胶质瘤干细胞膜(CMs),用于靶向根除GSCs及其相关肿瘤细胞。鉴定的纳米体通过各种方法进行了广泛的表征。在体外和体内进行了纳米材料的应用试验。在体外和体内对纳米系统的肿瘤抑制作用进行了评价。FDPM可以在磁引导下进行人工定向,同时继承CM的多种生物功能。经静脉注射后,FDPM被磁吸引到肿瘤部位,在CM的帮助下穿过血脑屏障。其同源靶向能力来源于CM上的活性蛋白,使其能够特异性靶向GSCs及相关肿瘤细胞。包裹在纳米颗粒内的阿霉素(DOX)随后摧毁了这些肿瘤细胞。FDPM具有良好的生物相容性和肿瘤靶向性,可有效靶向由GSCs引发的恶性胶质瘤。FDPM能显著减少肿瘤细胞,抑制肿瘤生长,显著延长胶质瘤裸鼠的存活时间。这些发现表明FDPM是一种很有前景的靶向GSCs和相关肿瘤细胞的纳米平台,可以提高胶质瘤的治疗效果。
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A Magnetic-Responsive Biomimetic Nanosystem Coated with Glioma Stem Cell Membranes Effectively Targets and Eliminates Malignant Gliomas.

Glioblastoma multiforme (GBM) is among the most challenging malignant brain tumors, making the development of new treatment strategies highly necessary. Glioma stem cells (GSCs) markedly contribute to drug resistance, radiation resistance, and tumor recurrence in GBM. The therapeutic potential of nanomaterials targeting GSCs in GBM urgently needs to be explored. A magnetic-responsive biomimetic nanosystem (FDPM), coated with glioma stem cell membranes (CMs), was designed for the targeted eradication of GSCs as well as their associated tumor cells. Identified nanobodies were extensively characterized with various assays. The application tests on nanomaterials were conducted in vitro and in vivo. The tumor-suppressive effects of the nanosystem were evaluated in vitro and in vivo. FDPM can be artificially directed under magnetic guidance while inheriting various biological functions from CM. Upon intravenous injection, FDPM was drawn to the tumor site by magnetic attraction, where it could cross the blood-brain barrier aided by CM. Its homologous targeting ability originates from active proteins on CM, enabling it to specifically target GSCs and related tumor cells. The encapsulated doxorubicin (DOX) within the nanoparticle then destroyed these tumor cells. FDPM demonstrated excellent biocompatibility and tumor-targeting efficiency, effectively targeting malignant gliomas initiated by GSCs. FDPM significantly reduced tumor cells, inhibited tumor growth, and notably extended the survival of glioma-bearing nude mice. The findings position FDPM as a promising nanoplatform to target GSCs and related tumor cells for improving the therapeutic effect of glioma.

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