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Cross-regulations among NRFs and KEAP1 and effects of their silencing on arsenic-induced antioxidant response and cytotoxicity ors human keratinocytes.

BACKGROUND: Nuclear factor E2-related factors (NRFs), including NRF2 and NRF1, play critical roles in mediating the cellular adaptive response to oxidative stress. Human exposure to inorganic arsenic, a potent oxidative stressor, causes various dermal disorders, including hyperkeratosis and skin cancer.

OBJECTIVE: We investigated the cross-regulations among NRF2, NRF1, and KEAP1, a cullin-3 adapter protein that allows NRF2 to be ubiquinated and degraded by the proteasome complex, in arsenic-induced antioxidant responses.

RESULTS: In human keratinocyte HaCaT cells, selective knockdown (KD) of NRF2 by lentiviral short hairpin RNAs (shRNAs) significantly reduced the expression of many antioxidant enzymes and sensitized the cells to acute cytotoxicity of inorganic arsenite (iA[s.sup.3+]). In contrast, silencing KEAP1 led to a dramatic resistance to iA[s.sup.3+]-induced apoptosis. Pretreatment of HaCaT cells with NRF2 activators, such as tert-butylhydroquinone, protects the cells against acute iA[s.sup.3+] toxicity in an NRF2-dependent fashion. Consistent with the negative regulatory role of KEAP 1 in NRF2 activation, KEAP1-KD cells exhibited enhanced transcriptional activity of NRF2 under nonstressed conditions. However, deficiency in KEAP1 did not facilitate induction of NRF2-target genes by iA[s.sup.3+]. In addition, NRF2 silencing reduced the expression of KEAP1 at transcription and protein levels but increased the protein expression of NRF1 under the iA[s.sup.3+]-exposed condition. In contrast, silencing KEAP1 augmented protein accumulation of NRF2 under basal and iA[s.sup.3+]-exposed conditions, whereas the iA[s.sup.3+]-induced protein accumulation of NRF1 was attenuated in KEAP1-KD cells.

CONCLUSIONS: Our studies suggest that NRF2, KEAP1, and NRF1 are coordinately involved in the regulation of the cellular adaptive response to lA[s.sup.3+]-induced oxidative stress

KEY WORDS: antioxidant response, arsenic, cytotoxicity, KEAP1, keratinocyte, NRF1, NRF2. Environ Health Perspect 120:583-589 (2012). http://dx.doi.org/10.1289/ehp.1104580 [Online 3 January 2012]

Arsenic (As) is a natural element that is ubiquitous in the environment in both organic and inorganic forms. Human exposure to inorganic arsenic (iAs), the more toxic form, occurs in environmental and occupational settings, as well as through medicinal arsenical use (Abernathy et al. 1999; Aposhian and Aposhian 2006). The skin is one of the most sensitive organs to chronic iAs toxicity. Arsenic-induced nonmalignant skin lesions, including hyperkeratosis and dyspigmentation, are some of the most common and earliest signs of chronic iAs exposure (Pi et al. 2000; Yoshida et al. 2004). Skin cancers associated with human iAs exposure include squamous cell carcinoma, basal cell carcinoma, intraepi-dermal carcinoma, and Bowen's disease (carcinoma in situ) (Alain et al. 1993; International Agency for Research on Cancer 2004; Schwartz 1996; Wong et al. 1998). Although As is a well-established human skin toxicant, the underlying molecular mechanism(s) is still unclear. Accumulating evidence reveals that oxidative stress occurs in response to inorganic arsenite (iA[s.sup.3+]) exposure (Pi et al. 2002, 2003b; Zhao et al. 2011), which may account for the dermal toxicity induced by iA[s.sup.3+], including hyperkeratosis and carcinogenesis.

Nuclear factor erythroid-derived factor 2 related factor 2 (NRF2), which belongs to the cap 'n' collar (CNC) subfamily of basic-region leucine zipper (bZIP) transcription factors, is a central regulator in the cellular adaptive antioxidant response to oxidative stress (Villeneuve et al. 2010; Zhang 2010). The CNC subfamily also includes NRF1 (NFE2L1/LCRF1/TCF11), NRF3 (NFE2L3), and the nuclear factor-erythroid 2 p45 subunit, as well as more distantly related factors such as BTB and CNC homology 1 (BACH1) and BACH2 protein. Under non-stressed conditions, NRF1 is targeted to the endoplasmic reticulum (Biswas and Chan 2010), whereas NRF2 is primarily in the cytoplasm. When cells are under oxidative stress, NRF2 and/or NRF1 dimerize with small Maf or other bZIP proteins in the nucleoplasm, and the heterodimer binds to the cis-acting element(s) called antioxidant response elements (AREs) in the promoters of target genes, leading to their transcriptional activation (Biswas and Chan 2010; Maher and Yamamoto 2010). Kelch-like ECH-associated protein 1 (KEAP1), a cytoplasmic protein, serves as a substrate-adaptor molecule for cullin-3 based ubiquitin E3 ligase (Kobayashi et al. 2004; Zhang 2010). Under nonstressed conditions, KEAP1 binds to NRF2 and represses the activity of NRF2 by promoting its ubiquitination and proteasome-dependent degradation (Kobayashi et al. 2004; Villeneuve et al. 2010). When cells are exposed to electrophiles or oxidants, modification of the sulthydryl groups in KEAP1 occurs, liberating NRF2 from KEAP1-mediated degradation, and NRF2 accumulates in the nucleus (Dinkova-Kostova et at 2002; Motohashi and Yamamoto 2004). Fibroblasts derived from Ntfl-mutant mouse embryos and human keratinocytes with NR17.1 knockdown (KD) showed reduced glutathione (GSH) levels and higher sensitivity to the toxic effects of oxidants, including iAs.[sup.3+] -(Kwong et al. 1999; Zhao et al. 2011), suggesting a critical role for NRF1 in cellular oxidative defense. Although previous studies have suggested that N RF I interacts with KEAP1 (Biswas and Chan 2010; Zhao et al. 2011), the biological significance of this interaction is still poorly characterized. In particular, the cross-regulations among NRF2, KEAP I, and NRF 1 under oxidative stress conditions have not been fully investigated.

Previous studies (Aono et al. 2003), including our own (Pi et al. 2003b), suggested that NRF2 is a key player in the cellular adaptive response to iA[sup.3+] -induced oxidative stress, whereas constitutive NRF2 activation may be involved in arsenic carcinogenesis (Pi et al. 2008a). Our recent studies also demonstrated that long isoforms of NRF1 contribute to iAs3t-induced antioxidant response in human keratinocytes and protect the cells from acute arsenic cytotoxicity (Zhao et al. 2011). In the present study, the roles of NRF2 and KEAPI in iA[sup.3+]-induced cytotoxicity and apoptosis, as well as the cross-regulations among NRF2, KEAPI, and NRF1 in response to acute iA[sup.3+] exposure, were studied by using human keratinocyte HaCaT cells with selective knockdown of IV R172 and KEAPI by lentiviral delivery of short hairpin RNAs (shRNAs). We demonstrated that cross-talk among NRF2, KEAPI, and NRF1 is an important part of iA[sup.3+]-induced antioxidant response and contributes to the coordinate regulation of antioxidant and detoxification enzyme expression, thus protecting cells from arsenic-induced apoptosis and cytotoxicity. Together with our previous findings (Zhao et al. 2011), we propose a comprehensive regulatory mechanism for iA[sup.3+]-induced adaptive antioxidant response in target cells of arsenic exposure, which may help advance our understanding of the mechanisms by which arsenic causes skin disorders.

Materials and Methods

Reagents and cell culture. Sodium arsenite and tert-burylhydroquinone (tBH.Q) were obtained from Sigma (St. Louis, MO, USA). The HaCaT cell is a spontaneously immortalized human epithelial cell line developed by Boukamp et al. (1988). The cells were cultured in Dulbecco's modified Eagle's medium supplemented with 10% fetal bovine serum (FBS), 100 U penicillin/mt., and 100 pg streptomycin/mL, as described previously (Pi et al. 2003b). Cultures were maintained at 37 [degrees] C in a humidified 5% C[O.sub.2] atmosphere. Culture media, FBS, and supplements were purchased from Invitrogen (Carlsbad, CA, USA).

Lentiviral-based shRNA transduction. MISSION shRNA lentiviral particles were obtained from Sigma. Transduction of HaCaT cells with lentiviral-based shRNAs targeting NRF2 (SHVRS-NM_006164), KEAPI (SHVRS-NM 012289) or scrambled non-target negative control (SHC002V) was performed as described previously (Zhao et al.2011). Cells were maintained in medium containing 1.0 pg/mL puromycin.

Quantitative real-time reverse-transcriptase polymerase chain (RT-PCR) reaction analysis. Total RNA was isolated with TRIzol (Invitrogen) and then subjected to cleanup by using the RNase-Free DNase Set and the RNeasy Mini kit (Qiagen, Valencia, CA, USA). Quantitative real-time RT-PCR was performed as described previously (Zhao et al. 2011). Primers [sequences are shown in Supplemental Material, Table 1 (http://dx.doi.org/10.1289/ehp.1104580)] were designed by using Primer Express 4 (Applied Biosyscems, Carlsbad, CA, USA) and synthesized by MWG Biotech Inc. (High Point, NC, USA). Real-time fluorescence detection was carried out by using an Applied Biosystems 79001HT Fast Real-Time PCR System (Applied Biosystems).

Western blot analysis. Protein isolation from whole-cell lysates and Western blotting were performed as detailed previously (Pi et al.2003b; Zhao et al. 2011). Antibodies for NRF2 (sc-13032; 1:500), KEAP1 (sc-15246; 1:500), NRF1 (sc-13031; 1:500), and heme oxyge-nase 1 (HMOX-1; sc-136902; 1:500) were purchased from Santa Cruz Biotechnology Inc. (Santa Cruz, CA, USA). Antibody for NAD(P)H:quinone oxidoreductase 1 (NQ01; 39-3700; 1:1,000) was purchased from Invitrogen. Antibodies for [beta]-ACTIN (A1978; 1:2,000) and glutamate-cysteine ligase, cata-lytic subunit (GCLC; RB-1697; 1:800) were from Sigma and Lab Vision (Fremont, CA, USA), respectively.

Measurement of intracellular GSH. Cells were sonicated in cold phosphate-buffered saline immediately after collection, followed by centrifugation at 12,000 x g for 5 min. The resulting supernatants were used for measurement of total GSH by using the BIOXYTECH GSH/GSSG-412 kit (OxisResearch, Portland, OR, USA) (Fu et al. 2010).

Acute cytotoxicity assay. A minimum of Ave replicates of 10,000 cells per well were plated in 96-well plates and allowed to adhere to the plate for 24 hr, at which time the media were removed and replaced with fresh media containing arsenic compounds. Cells were then incubated for an additional 24 hr, and cell viability was determined by using the Non-Radioactive Cell-Proliferation Assay Kit (Promega, Madison, WI, USA) as detailed previously (Zhao et al. 2011). Measurements were expressed as percentage change from untreated control (vehicle) of appropriate cells. The concentrations that were lethal to 50% of cells (L[C.sub.50]) were determined from analysis of the log-linear phase of the curves.

Determination of apoptosis by flow cytometry. Cells were seeded in six-well plates and cultured to approximately 80% confluence. Twenty hours after iAs3+ exposure, the cells, including floating and attached cells, were harvested for apoptosis analysis. Detection of phosphatidylserine on the outer leaflet of apoptotic cells was performed using TAGS Annexin V-FITC (fluorescein isothiocynate) Apoptosis Detection Kit (Trevigen, Gaithersburg, MD, USA) as detailed previously (Pi et al. 2005). For each sample, 10,000 cells were examined by flow cytometry (FACS Vantage; Becton Dickinson, San Jose, CA, USA). Percentage of apoptotic cells (annexin V positive) was determined by statistical analysis of the various dot plots with the BD FACS Diva, version 6.1.2 (BD Biosciences, Bedford, MA, USA).

Statistical analyses. All statistical analyses were performed using Graphpad Prism 4 (GraphPad Software, San Diego, CA, USA), with p < 0.05 taken as significant. Data are expressed as mean SE. Statistical analyses to evaluate the effect of shRNAs on the gene expression of NRF2 and KEAPI and intracellular GSH levels were carried out by using one-way analysis of variance (ANOVA) with Tukey's or Dunnett's multiple comparison test. Statistical analyses to evaluate the time-and concentration-dependent effect of iA[s.sup.3+] exposure on gene expression and cell viability were performed by using two-way ANOVA with Bonferroni post hoc testing.

Results

Stable knockdown of NRF2 and KEAP 1 in HaCaT cells. To study the role of NRF2-mediated antioxidant response in iA[s.sup.3+]-induced cytotoxicity, we performed lentiviral shRNA-mediated knockdown of NRF2 and KEAP1 in HaCaT cells. As shown in Figure 1, five shRNAs were used to target each of the two genes. One construct (sh-NRF2-1) markedly silenced NRF2 expression compared with the scrambled nontarget negative control (SCR), whereas the other four NRF2 constructs had moderate silencing effects (Figure IA). The effectiveness of knockdown by sh-NRF2-1 (NRF2-KD) was further confirmed by notably diminished protein accumulation of NRF2 when induced by tBHQ, a potent NRF2 activator (Pi et al. 2007). Our previous data indicated that two phosphorylated forms of human NRF2 near 95-120 kDa accumulate in the nucleus after chemically induced oxidative stress, including acute iA[s.sup.3+] exposure (Pi et al. 2007). In the present study, both of the NRF2 bands were diminished by lentiviral shRNA-mediated knockdown, confirming that the silencing is effective and providing additional support for our previous findings (Pi et al. 2007). In addition, the protein expression of ARE-dependent genes NQ01 and GCLC was attenuated, indicating that the transcrip-tional activity of NRF2 was suppressed in the NRF2-KD cells (Figure 1 B).

Similarly, HaCaT cells transduced with construct sh-KEAP1-1 (KEAP1-KD) showed the most efficient knockdown of KEAPI expression (Figure 1C, D). Supporting the silencing effect of KEAPI, enhanced expression of NQ01 and GCLC was observed in KEAPI-KD cells with or without tBHQ treat-ment (Figure 1D). Based on the Ensembl database, the human KEAPI has two splice variant transcripts coding for the same protein of 624 amino acids with a predicted molecular weight (MW) of 69.7 kDa. However, our immunoblots (Figure 1 D) using an antibody developed against a peptide mapped near the Nterminus of human KEAP1 revealed two bands with apparent MW between 68 arid 75 kDa KEAP1-KD dramatically diminished both bands, suggesting that both represent endogenous human KEAP 1. Clearly, additional research is required to characterize the two isoforms of KEAP1.

The key enzymes that regulate de novo GSH synthesis, including GCLC, glutamate-cysteine ligase, modifier subunit (GCLM), and glutathione synthetase, are well-documented ARE-dependent genes. Thus, intracellular GSH is an important indicator for the transcriptional activity of NRF2. As shown in Figure 1E, the intracellular GSH level in NRF2-KD cells was significantly decreased, whereas KEAP1-KD cells exhibited a modest but statistically sig-nificant increase in the GSH level compared with that of SCR cells, confirming the silencing effect of NRF2 and KEAP1.

Stable knockdown of NRF2 results in attenuated antioxidant induction in response to iAincluding acute exposure. To define the role of NRF2-mediated antioxidant response in cellular defense against iA[s.sup.3+] toxicity, NRF2-KD and SCR cells were acutely exposed to iAs3+, and the expression of NRF2 and the ARE-dependent genes HMOX-1, NQ01, GCLC, GCLM, and sulfiredoxin (SRX) was determined [Figure 2A, B; see also Supplemental Material, Figure 1A, B (http://dx.doi.org/10.1289/ehp.1104580)]. In SCR cells, iA[s.sup.3+] concentration-and time-dependently increased NRF2 and ARE-dependent gene expression at both mRNA (Figure 2A; see also Supplemental Material, Figure 1A) and protein (Figure 2B; see also Supplemental Material, Figure 1B) levels, confirming our previous findings that iA[s.sup.3+] is a potent NRF2 activator (Pi et al. 2003b, 2007). In contrast, NRF2-KD cells exhibited dramatically attenuated expression of NRF2 and ARE-dependent genes under both basal and iAincluding acute-exposed conditions (Figure 2A, B; see also Supplemental Material, Figure 1A, B).

Stable knockdown of KEAP 1 results in enhanced basal expression of ARE-dependent genes but weakens iAincluding acute-induced antioxidant response. Consistent with the inhibitory role of KEAP1 in regulating NRF2-ARE activity, KEAP1-KD cells exhibited enhanced expression of the ARE-dependent genes HMOX-1, NQ01, SRX1, GCLC, and GCLM under basal conditions [Figure 2C, D; see also Supplemental Material, Figure 1C, D http://dx.doi.org/10.1289/ehp.1104580)]. In apparent contrast to the enhanced basal expression, deficiency in KEAP1 diminished iA[s.sup.3+]-induced expression of HMOX-1 at mRNA and protein levels (Figure 2C, D; see also Supplemental Material, Figure 1C, D). In addition, no constant increase in iAincluding acute-induced expression of other ARE-dependent genes was observed in KEAP1-KD cells. These findings suggest that constitutive activation of NRF2 may weaken the induction of ARE-dependent genes, in particular HMOX-1, in response to acute iA[s.sup.3+] exposure. Note that acute exposure (6 hr) to high concentrations of iA[s.sup.3+] (20-40 i.tM) suppressed KEAP1 expression in SCR cells (Figure 2C, D), which might contribute to high-concentration iA[s.sup.3+]-induced NRF2 activation.

Cross-regulations among NRF2, KEAP 1, and NRF1 in iA[s.sup.3+] -induced antioxidant response in HaCaT cells. Although the manner in which NRF2 is regulated by KEAPI has been well documented, the effect of NRF2 deficiency on expression of KEAP I is not clear, in particular under oxidative stress conditions. As shown in Figure 3, lack of NRF2 resulted in attenuated gene and protein expression of KEAP1 under basal and iA[s.sup.3+]-exposed conditions, suggesting that the expression of KEAP1 is dependent on NRF2. Although deficiency of NRF2 did not increase the mRNA expression of NM (Figure 3A, C), NRF2-ICD cells exhibited increased protein accumulation of NRF 1 under high concentrations of iA[s.sup.3+] (2.5-20 [micro]M for 6 hr and 10 [micro]M for 6-24 hr), suggesting that NRF1 may compensate for the deficiency of NRF2 under iA[s.sup.3+]-exposed conditions to protect the cells from oxidative damage. In addition, an induction in NRF1 protein levels was observed in SCR cells but was short-lived compared with the sustained response observed in NRF2-KD cells (Figure 3D). In contrast, knockdown of KEAP1 augmented the protein accumulation of NRF2 under basal and iA[s.sup.3+]-exposed conditions (Figure 4). Conversely, KEAP1-KD cells exhibited reduced protein level, but not mRNA expression, of NRF1 induced by high concentrations of iA[s.sup.3+] (> 5 [micro]M; Figure 4). The weakened protein accumulation of NRF1 in response to high concentrations of iA[s.sup.3+] in KEAP1-KD cells could result from enhanced NRF2-mediated antioxidant response, leading to augmented detoxification capacity and/or lowered intracellular iA[s.sup.3+] level. The difference between mRNA and protein expression of NRF1 suggests that protein stabilization is a major mechanism for N REI activation, which is consistent with a recent report (Steffen et al. 2010).

Distinct effect of knockdown of NRF2 or KEAP I on iA[s.sup.3+]-induced cytotoxicity and apoptosis in HaCar cells. To investigate the roles of NRF2 in iA[s.sup.3+]-induced cytotoxicity, acute (24 hr) effects of iAs3+ exposure on cell metabolic integrity were measured in NRF2-KD and KEAPI-KD HaCaT cells. As shown in Figure 5A, deficiency of NM significantly enhanced the cells' sensitivity to iAs.[sup.3+] toxicity. The I., C50 value was 16.3 [+ or -] 2.5 [micro]M in NRF2-KD cells versus 36.0 [+ or -] 2.] [micro]M in SCR cells (p < 0.05). In contrast, knockdown of KEAPI led to a dramatic resistance to Ass* toxicity (Figure 5A). The L[C.sub.50] value in the KEAPI-KD cells was 80.1 [+ or -] 3.1 [micro]M, which was significantly higher than that of SCR. We then measured iA[s.sup.3+]-induced apoptosis and necrosis using flow cytometry with annexin V-FITC and pro-pidum iodide double staining. Consistent with the results of cytotoxicity, knockdown of NRF2 in HaCaT cellsdramatically enhanced the sensitivity to iA[s.sup.3+]-induced apoptosis, whereas deficiency of KEAPI led to a significant apoptotic resistance (Figure 5B).

To provide further support of our hypothesis that NRF2 activation contributes to iA[s.sup.3+]-induced apoptotic resistance, the effect of pretreatment of HaCaT cells with NRF2 activator tBHQ on iA[s.sup.3+]-induced cytotoxicity was examined. As shown in Figure 5C, pre-treatment of SCR cells with noncytotoxic level of tBHQ (25 [micro]M) for 6 hr modestly but statistically significantly protected the cells from subsequent cytotoxicity induced by high concentrations of iA[s.sup.3+]. However, pretreatment of NRF2-KD cells with tBHQ showed no protective effect against iA[s.sup.3+] toxicity, suggesting that the protective effect of tBHQ pretreatment is a result of NRF2 activation. In addition, no further protective effect was observed by tBHQ pretreatment in KEAN-KD cells, possibly because NRF2 is already maximally activated in these cells and cannot be increased further by tBHQ. In contrast, the protective effect of pretreatment with noncytotoxic dose of iA[s.sup.3+] (2.5 [micro]M) revealed a somewhat different pattern. Although iA[s.sup.3+] pretreatment can protect against cytotoxicity subsequently induced by higher doses of iA[s.sup.3+] in SCR cells, the protection also exists in NRF2-KD cells, suggesting that low-dose iA[s.sup.3+]. might trigger, in addition to NRF2, other adaptive mechanisms, such as activation of NU-I (Figure 5D). Like tBHQ pretreatment, The [s.sup.3+] pretreatment did not provide further protection of KEAPI-KD cells from high-dose iA[s.sup.3+] toxicity. The finding that NRF2 activators exhibited less significant effect than KLAN silencing on cell survival after arsenic treatment suggests that knockdown of KEAP1 resulted in a higher level of antioxidant response than did tBHQ or arsenic pretreatment and/or that KEAPI silencing also activated an NRF2-independent mechanism to contribute to the protection.

Discussion

Supporting the importance of NRF2 in cellular defense is the finding that Nrf2-knockout mice show deficiency in the coordinated antioxidant and phase II gene induction program and have a higher susceptibility to both oxidative damage and chemical carcinogenesis (Chan et al. 2001; Ramos-Gomez et al. 2001). In addition, lack of NRF2 in various mammalian cells has been reported to be associated with heightened sensitivity to various oxidative insults, including iAs-induced and ultraviolet A induced apoptosis (Calkins et al. 2005; Hirota et al. 2005; Lee et al. 2003). In the present study, we provide evidence that NRF2 regulates many ARE-dependent genes and contributes to resistance to iA[s.sup.3+]-induced cytotoxicity and apoptosis in human keratinocytes. In apparent contrast to extensive data showing that lowered NRF2 activity predisposes cells to chemical carcinogenesis, emerging evidence reveals the dichotomy that constitutive activation of NRF2 may contribute to malignant phenotypes (Padmanabhan et al. 2006). Indeed, increased expression and activity of NRF2, resulting from mutations in KEAP1 and/or NRF2, have been observed in various tumor cells, including skin, breast, prostate, lung, head/neck, and endometrium (Kim et al. 2010; Ohta et al. 2008; Padmanabhan et al. 2006; Shibata et al. 2008; Singh et al. 2006; Stacy et al. 2006). In humans, NRF2 activation due to NRF2 or KliA.P1 gene mutation plays an important role in the development of skin squamous cell carcinoma (Kim et al. 2010), which is the most common type of skin cancer caused by chronic iAs exposure. Most recently, DeNicola et al. (2011) reported that oncogene-induced NRF2 transcription promotes reactive oxygen species (ROS) detoxification and tumorigenesis. These seemingly contradictory findings suggest that NRF2 may play paradoxical roles in different stages of tumorigenesis. On the one hand, NRF2-dependent antioxidant and detoxification enzymes may promote the detoxification and elimination of ROS and other carcinogens to alleviate their carcinogenic effect. On the other hand, NRF2 activation may provide cell survival advantage by contributing to acquired apoptotic resistance, which is an important event in the process of arsenic-induced malignant transformation in many cell types, including human keratinocytes (Pi er al. 2005, 2008b; Tokar et al. 2010). Therefore, the timing and cellular target of intervention targeting NRF2 are critically important for chemoprevention of cancers.

Hyperkeratosis is one the most common human skin disorders caused by chronic iAs exposure (Pi et al. 2000; Wong et al. 1998; Yoshida et al. 2004). The underlying mechanism is, however, poorly understood. iA[s.sup.3+] has been identified as a potent activator of NRF2-mediated antioxidant response (Pi et al. 2003a), whereas NRF2 and its target genes have been reported as important regulators in skinwound healing (Braun et al. 2002) and arsenic-induced skin injury (Pi et al. 2003b, 2008a). In the present study, we confirmed the stimulatory effect of iA[s.sup.3+] on NRF2 activation in human keratinocytes and demonstrated that high concentrations of iA[s.sup.3+] inhibit the expression of KEAP1, which may contribute to NRF2 activation by A[s.sup.3+]. It has been reported that disruption of Keapl in mice leads to hyperkeratosis in esophagus, forestomach, and skin, most likely because of constitutive activation of NRF2 and aberrant expression of some ARE-dependent cytokeratins (Wakabayashi et al. 2003). Therefore, iA[s.sup.3+]-induced persistent activation of NRF2 may be associated with the pathogenesis of skin hyperkeratosis, although additional studies are needed to confirm the linkage.

The distinctive roles of NRF2 and NRF1 in arsenic-induced keratinocyte toxicity have been demonstrated in our previous studies (Pi et al. 2003b, 2005, 2007, 2008a; Zhao et al. 2011). However, the cross-regulations among NRF2, NRF1, and KEAP1 in iA[s.sup.3+]-induced antioxidant response have not been investigated. In the present study, we observed higher levels of NRF1 protein accumulation in NRF2-KD cells than of SCR in response to high concentrations of iA[s.sup.3+]-exposure, suggesting that NRF1 may compensate for deficiency of NRF2 in iA[s.sup.3+]-induced antioxidant response. This is consistent with the finding by Braun et al. (2002) demonstrating that mice lacking NRF2 had no significant wound healing phenotype partially because of an up-regulation of NRF1. In contrast, silencing of NRF1 in HaCaT cells does not interfere with iA[s.sup.3+]-induced NRF2 protein accumulation, revealing that NRF2 cannot compensate for deficiency of NRF1 in iA[s.sup.3+]-induced antioxidant response (Zhao et al. 2011). In addition, reduced KEAP1 expression was observed in NR_FI-KD HaCaT cells, suggesting a potential regulation of KEAP1 by NRF1 (Zhao et al. 2011). In the present study, we found that lack of NRF2 also led to reduced expression of KEAP1. Taken together, the reduction in expression of KEAP1 in both NRF1-and NRF2-KD cells highly suggests that KEAP1 is an ARE-dependent gene. It is unclear whether such regulation, if indeed present, has any functional significance.

In contrast to increased expression of NRF2 and its target genes under basal conditions, a weakened induction of HMOX-1 by iA[s.sup.3+] was observed in KEAPI-KD cells. This finding is consistent with our previous study showing that persistent activation of NRF2 by chronic iA[s.sup.3+] exposure paradoxically represses NRF2-mediated antioxidant induction in response to additional acute oxidative challenges (Pi et al. 2008a). In addition, KEAP1-KD cells exhibited reduced protein levels of NRF1 induced by high concentrations of iA[s.sup.3+], suggesting a potential association between NRF 1 and KEAP1. Our previous study indicated that exogenous GSH markedly suppresses hypochlorous acid-induced NRF2 activation in mouse macrophages (Pi et al. 2008a), suggesting that the enhanced GSH levels in KEAP1-KD cells may be a critical factor for the weakened NRF2 activation. In addition, elevated levels of NRF2 and subsequent induction of phase II enzymes in KEAP1-KD cells might reduce the intracellular concentration of iA[s.sup.3+] and thus result in decreased activation of NRF2 and NRF1.

In summary, we provide evidence that NRF2, KEAP 1, and NRFI interact with each other and coordinate regulation of cellular adaptive antioxidant responses to acute iA[s.sup.3]+ exposure. Given the potential importance of oxidative stress in arsenic-induced dermal toxicity and carcinogenicity, as well as the critical roles of NRF2 and NRF 1 in defending against oxidative damage and the pathogenesis of skin cancer and hyperkeratosis, our findings provide an important insight into the mechanism for dermal toxicity induced by arsenic exposure.

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Flui Zhao, (1), (2) Yongyong Hou, (2) Qiang Zhang, (2) Courtney G. Woods, (2) Peng Xue, (2) Jingqi Fu, (2) Kathy Yarborough, (2) Dawei Guan, (1) Melvin E. Andersen, (2) and Jingbo Pi (2)

(1) School of Forensic Medicine, China Medical University, Shenyang, China; (2) Institute for Chemical Safety Sciences, Hamner Institutes for Health Sciences, Research Triangle Park, North Carolina, USA Address correspondence to J. Pi, Institute for Chemical Safety Sciences, Hamner Institutes for Health Sciences, 6 Davis Dr., Research Triangle Park, NC 27709 USA. Telephone: (919) 558-1395. Fax: (919) 558-1305. E-mail: jpi@thehamner.org

Supplemental Material is available online (http://dx.doi.org/10.1289/chp.1104580).

This work was supported in part by National Institutes of Health grant ES016005 (J.P.), Dow Chemical Company (M.B.A.), National Natural Science Foundation of China award 81102156 (R.Z.), and Shenyang Scientific and Technological Plan award F11-264-1-44 (R.Z.).

The content is solely the responsibility of the authors. All authors have agreed to its content. M.E.A. received some funding from Dow Chemical Company. All of the other authors declare they have no actual or potential competing financial interests.

R.Z., Y.H., Q.Z., C.G.W, P.X., J.F., K.Y., M.E.A., and J.P. are employees of the Hamner Institutes for Health Sciences. The Hamner is a 501(c)3 not-for-profit organization that has a diverse research portfolio that includes funding from the American Chemistry Council, a trade association that represents chemical manufacturers.

Received 4 October 2011; accepted 3 January 2012.
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Title Annotation:Research; nuclear factor E2-related factors; kelch-like ECH-associated protein 1
Author:Zhao, Rui; Hou, Yongyong; Zhang, Qiang; Woods, Courtney G.; Xue, Peng; Jinggi, Fu, Jingqi; Yarboroug
Publication:Environmental Health Perspectives
Article Type:Report
Geographic Code:1USA
Date:Apr 1, 2012
Words:5981
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