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时间分辨研究胺修饰聚苯乙烯纳米颗粒诱导的细胞死亡机制。

Time resolved study of cell death mechanisms induced by amine-modified polystyrene nanoparticles.

机构信息

Centre for BioNano Interactions and Conway Institute of Biomolecular and Biomedical Research, University College Dublin, Belfield, Dublin 4, Ireland.

出版信息

Nanoscale. 2013 Nov 21;5(22):10868-76. doi: 10.1039/c3nr03249c. Epub 2013 Oct 9.

Abstract

Positively charged polymers and nanoparticles (NPs) can be toxic to cells in various systems. Using human astrocytoma cells, we have previously shown that 50 nm amine-modified polystyrene NPs damage mitochondria and induce cell death by apoptosis. Here we provide comprehensive details of the cellular events occurring after exposure to the NPs in a time-resolved manner. We demonstrate that the accumulation of NPs in lysosomes plays a central role in the observed cell death, leading to swelling of the lysosomes and release of cathepsins into the cytosol, which ultimately propagates the damage to the mitochondria with subsequent activation of apoptosis. This is accompanied and sustained by other events, such as increasing ROS levels and autophagy. Using various inhibitors, we also show the interplay between apoptosis and autophagy as a response to NP accumulation in lysosomes.

摘要

带正电荷的聚合物和纳米粒子(NPs)在各种系统中都可能对细胞有毒。我们之前用人星形细胞瘤细胞证明,50nm 胺修饰的聚苯乙烯 NPs 通过凋亡诱导细胞死亡破坏线粒体。在这里,我们以时间分辨的方式提供暴露于 NPs 后细胞中发生的全面详细的事件。我们证明 NPs 在溶酶体中的积累在观察到的细胞死亡中起核心作用,导致溶酶体肿胀和组织蛋白酶释放到细胞质中,这最终导致线粒体损伤,随后激活凋亡。这伴随着其他事件的发生,例如 ROS 水平的增加和自噬。使用各种抑制剂,我们还显示了凋亡和自噬之间的相互作用,作为对溶酶体中 NP 积累的反应。

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