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锌、镉和镍会增加 NF-κB 的激活和 THP-1 单核细胞细胞因子的释放。

Zinc, cadmium and nickel increase the activation of NF-κB and the release of cytokines from THP-1 monocytic cells.

机构信息

REQUIMTE, Departamento de Ciências Químicas, Faculdade de Farmácia, Universidade do Porto, Rua Aníbal Cunha, 164, 4099-030 Porto, Portugal.

出版信息

Metallomics. 2011 Nov;3(11):1238-43. doi: 10.1039/c1mt00050k. Epub 2011 Aug 15.

Abstract

The sustained activation of the transcription factor nuclear factor κB (NF-κB) by metal-activated signalling pathways can lead to chronic inflammatory processes and related diseases, including carcinogenesis. The aim of the present work was to clarify the effect of zinc, nickel and cadmium on NF-κB activation in the THP-1 human monocytic leukemia cell line. The production of the NF-κB downstream pro-inflammatory mediators tumor necrosis factor (TNF)-α and interleukin (IL)-1β, IL-6 and IL-8 was also evaluated due to their important roles in the pathogenesis of chronic inflammatory and autoimmune diseases and, ultimately, in the development of cancer. The results obtained demonstrated that zinc, nickel and cadmium significantly activate NF-κB, and the release of the chemokine IL-8. Cadmium also induced the release of TNF-α and IL-6 in THP-1 monocytic cells, which may indicate some potential to induce deleterious effects through this pathway.

摘要

金属激活信号通路对转录因子核因子 κB(NF-κB)的持续激活可导致慢性炎症过程和相关疾病,包括癌症发生。本工作旨在阐明锌、镍和镉对 THP-1 人单核白血病细胞系中 NF-κB 激活的影响。由于肿瘤坏死因子(TNF)-α和白细胞介素(IL)-1β、IL-6 和 IL-8 等下游促炎介质在慢性炎症和自身免疫性疾病发病机制中的重要作用,最终在癌症发展中发挥作用,因此还评估了它们的产生。结果表明,锌、镍和镉可显著激活 NF-κB,并释放趋化因子 IL-8。镉还诱导 THP-1 单核细胞中 TNF-α和 IL-6 的释放,这可能表明通过该途径诱导有害作用的一些潜力。

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