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Caco-2 和 MCF-7 细胞对银纳米颗粒的不同反应基于高度相似的作用机制。

Different responses of Caco-2 and MCF-7 cells to silver nanoparticles are based on highly similar mechanisms of action.

机构信息

a RIKILT - Wageningen University & Research Centre , Wageningen , The Netherlands and.

b University College Dublin , Dublin , Ireland.

出版信息

Nanotoxicology. 2016 Dec;10(10):1431-1441. doi: 10.1080/17435390.2016.1225132. Epub 2016 Sep 6.

Abstract

The mode of action of silver nanoparticles (AgNPs) is suggested to be exerted through both Ag and AgNP dependent mechanisms. Ingestion is one of the major NP exposure routes, and potential effects are often studied using Caco-2 cells, a well-established model for the gut epithelium. MCF-7 cells are epithelial breast cancer cells with extensive well-characterized toxicogenomics profiles. In the present study, we aimed to gain a deeper understanding of the cellular molecular responses in Caco-2 and MCF-7 cells after AgNP exposure in order to evaluate whether epithelial cells derived from different tissues demonstrated similar responses. These insights could possibly reduce the size of cell panels for NP hazard identification screening purposes. AgNPs of 20, 30, 60, and 110 nm, and AgNO were exposed for 6 h and 24 h. AgNPs were shown to be taken up and dissolve intracellularly. Compared with MCF-7 cells, Caco-2 cells showed a higher sensitivity to AgNPs, slower gene expression kinetics and absence of NP size-dependent responses. However, on a molecular level, no significant differences were observed between the two cell types. Transcriptomic analysis showed that Ag(NP) exposure caused (oxidative) stress responses, possibly leading to cell death in both cell lines. There was no indication for effects specifically induced by AgNPs. Responses to AgNPs appeared to be induced by silver ions released from the AgNPs. In conclusion, differences in mRNA responses to AgNPs between Caco-2 and MCF-7 cells were mainly related to timing and magnitude, but not to a different underlying mechanism.

摘要

银纳米粒子(AgNPs)的作用模式被认为是通过 Ag 和 AgNP 依赖的机制发挥的。摄入是 NP 暴露的主要途径之一,经常使用 Caco-2 细胞来研究潜在的影响,Caco-2 细胞是一种成熟的肠道上皮模型。MCF-7 细胞是上皮性乳腺癌细胞,具有广泛的、特征明确的毒理基因组学特征。在本研究中,我们旨在更深入地了解 Caco-2 和 MCF-7 细胞在 AgNP 暴露后的细胞分子反应,以评估来自不同组织的上皮细胞是否表现出相似的反应。这些见解可能会减少用于 NP 危害识别筛选目的的细胞面板的大小。我们用 20nm、30nm、60nm 和 110nm 的 AgNPs 以及 AgNO 进行了 6 小时和 24 小时的暴露实验。结果表明,AgNPs 被细胞摄取并在细胞内溶解。与 MCF-7 细胞相比,Caco-2 细胞对 AgNPs 更为敏感,基因表达动力学较慢,且不存在 NP 尺寸依赖性反应。然而,在分子水平上,两种细胞类型之间没有观察到显著差异。转录组分析表明,Ag(NP)暴露引起(氧化)应激反应,可能导致两种细胞系的细胞死亡。没有迹象表明 AgNPs 有特定的作用。AgNPs 的反应似乎是由 AgNPs 释放的银离子诱导的。总之,Caco-2 和 MCF-7 细胞对 AgNPs 的 mRNA 反应的差异主要与时间和幅度有关,而不是与不同的潜在机制有关。

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