Literature DB >> 14567983

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

Jingbo Pi1, Wei Qu, Jeffrey M Reece, Yoshito Kumagai, Michael P Waalkes.   

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.

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Year:  2003        PMID: 14567983     DOI: 10.1016/s0014-4827(03)00341-0

Source DB:  PubMed          Journal:  Exp Cell Res        ISSN: 0014-4827            Impact factor:   3.905


  81 in total

1.  Nuclear factor erythroid-derived factor 2-related factor 2 regulates transcription of CCAAT/enhancer-binding protein β during adipogenesis.

Authors:  Yongyong Hou; Peng Xue; Yushi Bai; Dianxin Liu; Courtney G Woods; Kathy Yarborough; Jingqi Fu; Qiang Zhang; Guifan Sun; Sheila Collins; Jefferson Y Chan; Masayuki Yamamoto; Melvin E Andersen; Jingbo Pi
Journal:  Free Radic Biol Med       Date:  2011-10-28       Impact factor: 7.376

2.  Inflammatory macrophages induce Nrf2 transcription factor-dependent proteasome activity in colonic NCM460 cells and thereby confer anti-apoptotic protection.

Authors:  Susanne Sebens; Iris Bauer; Claudia Geismann; Evelin Grage-Griebenow; Stefan Ehlers; Marie-Luise Kruse; Alexander Arlt; Heiner Schäfer
Journal:  J Biol Chem       Date:  2011-10-11       Impact factor: 5.157

3.  Coordinated regulation of Nrf2 and histone H3 serine 10 phosphorylation in arsenite-activated transcription of the human heme oxygenase-1 gene.

Authors:  Paul D Ray; Bo-Wen Huang; Yoshiaki Tsuji
Journal:  Biochim Biophys Acta       Date:  2015-08-18

4.  Expression of Nrf2 and its downstream gene targets in hibernating 13-lined ground squirrels, Spermophilus tridecemlineatus.

Authors:  Pier Morin; Zhouli Ni; David C McMullen; Kenneth B Storey
Journal:  Mol Cell Biochem       Date:  2008-03-10       Impact factor: 3.396

5.  Hormesis and adaptive cellular control systems.

Authors:  Qiang Zhang; Jingbo Pi; Courtney G Woods; Annie M Jarabek; Harvey J Clewell; Melvin E Andersen
Journal:  Dose Response       Date:  2008-03-19       Impact factor: 2.658

6.  Arsenic transformation predisposes human skin keratinocytes to UV-induced DNA damage yet enhances their survival apparently by diminishing oxidant response.

Authors:  Yang Sun; Chikara Kojima; Colin Chignell; Ronald Mason; Michael P Waalkes
Journal:  Toxicol Appl Pharmacol       Date:  2011-07-21       Impact factor: 4.219

7.  Sporadic activation of an oxidative stress-dependent NRF2-p53 signaling network in breast epithelial spheroids and premalignancies.

Authors:  Elizabeth J Pereira; Joseph S Burns; Christina Y Lee; Taylor Marohl; Delia Calderon; Lixin Wang; Kristen A Atkins; Chun-Chao Wang; Kevin A Janes
Journal:  Sci Signal       Date:  2020-04-14       Impact factor: 8.192

8.  Enhanced glutathione biosynthetic capacity promotes resistance to As3+-induced apoptosis.

Authors:  James A Thompson; Christopher C Franklin
Journal:  Toxicol Lett       Date:  2009-12-16       Impact factor: 4.372

9.  Arsenic inhibits autophagic flux, activating the Nrf2-Keap1 pathway in a p62-dependent manner.

Authors:  Alexandria Lau; Yi Zheng; Shasha Tao; Huihui Wang; Samantha A Whitman; Eileen White; Donna D Zhang
Journal:  Mol Cell Biol       Date:  2013-04-15       Impact factor: 4.272

10.  Low-level arsenic impairs glucose-stimulated insulin secretion in pancreatic beta cells: involvement of cellular adaptive response to oxidative stress.

Authors:  Jingqi Fu; Courtney G Woods; Einav Yehuda-Shnaidman; Qiang Zhang; Victoria Wong; Sheila Collins; Guifan Sun; Melvin E Andersen; Jingbo Pi
Journal:  Environ Health Perspect       Date:  2010-01-25       Impact factor: 9.031

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