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AMPK 介导滞留在线粒体或溶酶体中的氧化铁纳米颗粒的神经毒性。

AMPK mediates the neurotoxicity of iron oxide nanoparticles retained in mitochondria or lysosomes.

机构信息

CAS Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety, Multidisciplinary Research Division, Institute of High Energy Physics, Chinese Academy of Sciences (CAS), Beijing 100049, China.

出版信息

Metallomics. 2019 Jul 17;11(7):1200-1206. doi: 10.1039/c9mt00103d.

Abstract

Environmental factors may play a critical role in the etiology and pathogenesis of Parkinson's disease (PD). However, the association of PD with specific chemical species remains largely unknown. Here we prepared three kinds of iron oxide nanoparticles and examined their cytotoxicity in a cellular model of PD. We found that lysosome-targeted nanoparticles showed significant cytotoxicity in SH-SY5Y cells. Inhibition of AMPK could aggravate the neurotoxicity of lysosome-targeted nanoparticles as well as mitochondrion-targeted nanoparticles. Alteration of mitochondrial membrane potentials was found to be in agreement with the neurotoxicity of iron nanoparticles. These results suggested an important role of AMPK in regulating iron nanoparticle-associated neurotoxicity.

摘要

环境因素可能在帕金森病 (PD) 的病因和发病机制中起关键作用。然而,PD 与特定化学物质的关联在很大程度上仍然未知。在这里,我们制备了三种氧化铁纳米颗粒,并在 PD 的细胞模型中检查了它们的细胞毒性。我们发现溶酶体靶向纳米颗粒在 SH-SY5Y 细胞中表现出显著的细胞毒性。AMPK 的抑制作用可加重溶酶体靶向纳米颗粒和线粒体靶向纳米颗粒的神经毒性。发现线粒体膜电位的改变与铁纳米颗粒的神经毒性一致。这些结果表明 AMPK 在调节铁纳米颗粒相关的神经毒性中起重要作用。

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