Nrf2-mediated adaptive response to cadmium-induced toxicity involves protein kinase C delta in human 1321N1 astrocytoma cells

被引:20
作者
Lawal, Akeem O. [1 ]
Ellis, Elizabeth M. [1 ]
机构
[1] Univ Strathclyde, Strathclyde Inst Pharm & Biomed Sci, Glasgow G1 1XW, Lanark, Scotland
关键词
Cadmium; Nrf2; Keap1; Antioxidants; Cytosolic; Nuclear; PKC delta; PKC; SOD1; GSTA1; NQO1; Rottlerin; Transcription; HEME OXYGENASE-1 GENE; OXIDATIVE STRESS; TRANSCRIPTION FACTOR; INTRACELLULAR CALCIUM; ACTIVATION; NRF2; ELEMENT; MECHANISMS; PATHWAY; PHOSPHORYLATION;
D O I
10.1016/j.etap.2011.03.010
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Cadmium (Cd) is a toxic heavy metal, and exposure to Cd causes a range of changes within the cell. At high concentrations, Cd causes damage to cells via a range of mechanisms. At low concentrations, Cd can stimulate expression of genes that are part of an adaptive response. In this study, we have used the astrocytoma cell line 1321N1 as a model to investigate the induction of protective enzymes in response to Cd. We have shown that expression of NAD(P)H:quinone oxidoreductase and haem oxygenase enzymes are induced as the protein level by -fold and -fold, and in response to 5 and 10 mu M Cd. Levels of NQ01 and HO1 mRNA are also increased by -fold and -fold following 24h exposure to 5 and 10 mu M cadmium. An increase in the nuclear accumulation of the transcription factor Nrf2 was also observed following Cd treatment. Through the use of the protein kinase C inhibitor bisindolylmaleimide (VIII) acetate we have demonstrated the involvement PKC in the Nrf2-mediated response of 1321N1 cells to 5-10 mu M Cd. We have also shown through the used of 10 mu M rottlerin that PKC delta is the isoform responsible for mediating this response. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:54 / 62
页数:9
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