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研究不同表面涂层量子点在体外引起氧化应激和影响巨噬细胞信号转导的潜力。

An investigation into the potential for different surface-coated quantum dots to cause oxidative stress and affect macrophage cell signalling in vitro.

机构信息

Centre for Nano Safety, School of Life Sciences, Edinburgh Napier University, Edinburgh, UK.

出版信息

Nanotoxicology. 2010 Jun;4(2):139-49. doi: 10.3109/17435390903276925.

Abstract

The aim of this study was to investigate the ability of a series of different surface-coated quantum dots (QDs) to cause oxidative stress and affect cell signalling in J774.A1 macrophages. Organic QDs caused a significant (p < 0.001) decrease in glutathione (GSH) levels over 24 h, while COOH and NH(2) (PEG) QDs induced a significant decrease (p < 0.05) in GSH at 6 and 24 h only. J774.A1 cytosolic Ca(2+) concentration significantly increased (p < 0.01) 30 min after treatment with all QDs. Trolox was, however, able to prevent the COOH and NH(2) (PEG) QD-induced Ca(2+) signal, but not the organic QD induced effect. All QDs tested were observed to have a relatively low ability to stimulate increased expression of the pro-inflammatory cytokine tumour necrosis factor-alpha (TNF-alpha). In conclusion, QDs differ in their interactions with macrophages according to their specific surface properties.

摘要

本研究旨在探究一系列不同表面涂层量子点(QD)引发氧化应激和影响 J774.A1 巨噬细胞信号转导的能力。有机 QD 在 24 小时内显著降低了(p < 0.001)谷胱甘肽(GSH)水平,而 COOH 和 NH(2)(PEG)QD 仅在 6 和 24 小时降低了 GSH(p < 0.05)。与所有 QD 处理后 30 分钟,J774.A1 细胞质 Ca(2+)浓度显著增加(p < 0.01)。然而,Trolox 能够防止 COOH 和 NH(2)(PEG)QD 诱导的 Ca(2+)信号,但不能阻止有机 QD 诱导的效应。所测试的所有 QD 都被观察到具有相对较低的刺激促炎细胞因子肿瘤坏死因子-α(TNF-α)表达增加的能力。总之,根据其特定的表面特性,QD 与巨噬细胞的相互作用存在差异。

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