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PMID: 14567983 Published · ppublish English Journal Article

Transcription factor Nrf2 activation by inorganic arsenic in cultured keratinocytes: involvement of hydrogen peroxide.

Experimental cell research ·Vol. 290 ·No. 2 ·2003-11-01 ·Pages 234-45

Pi J, Qu W, Reece JM, Kumagai Y, Waalkes MP

Abstract

Inorganic arsenic is a well-documented human carcinogen that targets the skin. The induction of oxidative stress, as shown with arsenic, may have a bearing on the carcinogenic mechanism of this metalloid. The transcription factor Nrf2 is a key player in the regulation of genes encoding for many antioxidative response enzymes. Thus, the effect of inorganic arsenic (as sodium arsenite) on Nrf2 expression and localization was studied in HaCaT cells, an immortalized human keratinocyte cell line. We found, for the first time, that arsenic enhanced cellular expression of Nrf2 at the transcriptional and protein levels and activated expression of Nrf2-related genes in these cells. In addition, arsenic exposure caused nuclear accumulation of Nrf2 in association with downstream activation of Nrf2-mediated oxidative response genes. Arsenic simultaneously increased the expression of Keap1, a regulator of Nrf2 activity. The coordinated induction of Keap1 expression and nuclear Nrf2 accumulation induced by arsenic suggests that Keap1 is important to arsenic-induced Nrf2 activation. Furthermore, when cells were pretreated with scavengers of hydrogen peroxide (H(2)O(2)) such as catalase-polyethylene glycol (PEG-CAT) or Tiron, arsenic-induced nuclear Nrf2 accumulation was suppressed, whereas CuDIPSH, a cell-permeable superoxide dismutase (SOD) mimic compound that produces H(2)O(2) from superoxide (*O(2)(-)), enhanced Nrf2 nuclear accumulation. These results indicate that H(2)O(2), rather than *O(2)(-), is the mediator of nuclear Nrf2 accumulation. Additional study showed that arsenic causes increased cellular H(2)O(2) production and that H(2)O(2) itself has the ability to increase Nrf2 expression at both the transcription and protein levels in HaCaT cells. Taken together, these data clearly show that arsenic increases Nrf2 expression and activity at multiple levels and that H(2)O(2) is one of the mediators of this process.

MeSH Terms
Arsenites/pharmacology Carrier Proteins/genetics,metabolism Cells, Cultured DNA Primers/chemistry DNA-Binding Proteins/genetics,metabolism Free Radical Scavengers/pharmacology Gene Expression Regulation Humans Hydrogen Peroxide/metabolism Keratinocytes/cytology,drug effects,metabolism Leucine Zippers NAD(P)H Dehydrogenase (Quinone)/metabolism NF-E2-Related Factor 2 Oxidation-Reduction Oxidative Stress RNA, Messenger/metabolism Receptors, G-Protein-Coupled/metabolism Reverse Transcriptase Polymerase Chain Reaction Sodium Compounds/pharmacology Superoxides/metabolism Trans-Activators/genetics,metabolism
Chemicals
Arsenites Carrier Proteins DNA Primers DNA-Binding Proteins Free Radical Scavengers NF-E2-Related Factor 2 NFE2L2 protein, human RNA, Messenger Receptors, G-Protein-Coupled Sodium Compounds Trans-Activators Superoxides sodium arsenite Hydrogen Peroxide NAD(P)H Dehydrogenase (Quinone) NQO1 protein, human
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Pi Jingbo
Inorganic Carcinogenesis Section, Laboratory of Comparative Carcinogenesis, NCI at NIEHS, National Institutes of Health, Research Triangle Park, NC 27709, USA.
Qu Wei
Reece Jeffrey M
Kumagai Yoshito
Waalkes Michael P
Article Info
Journal
Experimental cell research
Abbr.
Exp Cell Res
ISSN
0014-4827
Published
2003-11-01
Pages
234-45
Language
English
Region
United States
NLM ID
0373226
Subset
IM
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