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Cold Atmospheric Plasma Induces ATP-Dependent Endocytosis of Nanoparticles and Synergistic U373MG Cancer Cell Death

机译:寒冷的大气血浆诱导纳米颗粒的ATP依赖性内吞作用和协同的U373MG癌细胞死亡

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摘要

Gold nanoparticles (AuNP) have potential as both diagnostic and therapeutic vehicles. However, selective targeting and uptake in cancer cells remains challenging. Cold atmospheric plasma (CAP) can be combined with AuNP to achieve synergistic anti-cancer cytotoxicity. To explore synergistic mechanisms, we demonstrate both rate of AuNP uptake and total amount accumulated in U373MG Glioblastoma multiforme (GBM) cells are significantly increased when exposed to 75 kV CAP generated by dielectric barrier discharge. No significant changes in the physical parameters of AuNP were caused by CAP but active transport mechanisms were stimulated in cells. Unlike many other biological effects of CAP, long-lived reactive species were not involved, and plasma-activated liquids did not replicate the effect. Chemical effects induced by direct and indirect exposure to CAP appears the dominant mediator of enhanced uptake. Transient physical alterations of membrane integrity played a minor role. 3D-reconstruction of deconvoluted confocal images confirmed AuNP accumulation in lysosomes and other acidic vesicles, which will be useful for future drug delivery and diagnostic strategies. Toxicity of AuNP significantly increased by 25-fold when combined with CAP. Our data indicate that direct exposure to CAP activates AuNP-dependent cytotoxicity by increasing AuNP endocytosis and trafficking to lysosomes in U373MG cells.
机译:金纳米颗粒(AuNP)具有作为诊断和治疗载体的潜力。然而,癌细胞的选择性靶向和摄取仍然具有挑战性。可以将冷大气血浆(CAP)与AuNP结合使用,以达到协同的抗癌细胞毒性作用。为了探索协同机制,我们证明了当暴露于由介质阻挡放电产生的75 kV CAP时,U373MG多形胶质母细胞瘤(GBM)细胞中AuNP的摄取速率和累积的总量均显着增加。 CAP没有引起AuNP的物理参数的显着变化,但是激活了细胞中的主动转运机制。与CAP的许多其他生物学效应不同,没有涉及长寿命的反应性物质,并且血浆活化的液体不能复制这种效应。直接和间接暴露于CAP诱导的化学作用似乎是摄取增加的主要介质。膜完整性的暂时性物理改变起着较小的作用。去卷积共聚焦图像的3D重建证实了溶酶体和其他酸性囊泡中的AuNP积累,这将对将来的药物递送和诊断策略有用。当与CAP联合使用时,AuNP的毒性显着增加了25倍。我们的数据表明,直接暴露于CAP通过增加AuNP内吞作用和向U373MG细胞中的溶酶体的运输来激活AuNP依赖性细胞毒性。

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