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镉诱导的人细胞基因表达改变。

Cadmium-induced alterations of gene expression in human cells.

机构信息

Human Engineering and Risk Management Research Group, National Institute of Occupational Safety and Health, 6-21-1 Nagao, Tama-ku, Kawasaki 214-8585, Japan.

出版信息

Environ Toxicol Pharmacol. 2009 Jul;28(1):61-9. doi: 10.1016/j.etap.2009.02.007. Epub 2009 Feb 27.

Abstract

We have reported the changes in gene expression in human HeLa cells exposed to a low concentration (5μM) of Cd. In the present study, cells exposed to a higher concentration of Cd were analyzed using a DNA microarray with 9182 human cDNA probes, in an attempt to obtain a comprehensive view on the biological effects of Cd. After a 6h exposure to 50μM Cd, 48 genes were up-regulated 2.5-fold or greater and 14 genes were down-regulated to 40% or less. Marked up-regulation of genes coding for metallothioneins, anti-oxidant proteins, and heat shock proteins was observed. Cd appeared to repress cell proliferation by modulating genes involved in multiple pathways. Cd also affected a number of genes related to apoptosis. Interestingly, it appeared that a series of genes were regulated to accelerate the intrinsic pathway of apoptosis, while others were directed to suppress the extrinsic pathway. Of these, rapid and transient induction of the TR3 gene was noted as a possible key process in Cd-induced apoptosis. Effects on several genes that may reflect mechanistic backgrounds of Cd toxicity were also observed. The present study disclosed a complex pleiotypic response of human cells to Cd, which was composed of a variety of changes in gene expression directed to defense, growth arrest, recovery from damage, apoptosis and so on.

摘要

我们曾报道过人类 HeLa 细胞在低浓度(5μM)Cd 暴露下的基因表达变化。在本研究中,我们使用含有 9182 个人类 cDNA 探针的 DNA 微阵列分析了暴露于更高浓度 Cd 的细胞,试图全面了解 Cd 的生物学效应。在 50μM Cd 暴露 6 小时后,有 48 个基因的表达上调 2.5 倍或更高,有 14 个基因的表达下调至 40%或更低。观察到编码金属硫蛋白、抗氧化蛋白和热休克蛋白的基因明显上调。Cd 通过调节参与多种途径的基因似乎抑制了细胞增殖。Cd 还影响了许多与细胞凋亡相关的基因。有趣的是,似乎一系列基因被调节以加速细胞凋亡的内在途径,而其他基因则被导向抑制细胞凋亡的外在途径。在这些基因中,TR3 基因的快速和短暂诱导被认为是 Cd 诱导细胞凋亡的可能关键过程。还观察到了对一些可能反映 Cd 毒性机制背景的基因的影响。本研究揭示了人类细胞对 Cd 的复杂多效性反应,其中包括一系列旨在防御、生长停滞、损伤恢复、细胞凋亡等的基因表达变化。

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