A Review of the Evidence that Ochratoxin A Is an Nrf2 Inhibitor: Implications for Nephrotoxicity and Renal Carcinogenicity

Abstract

Several studies have demonstrated that ochratoxin A (OTA) inhibits the nuclear factor, erythroid 2-like 2 (Nrf2) oxidative stress response pathway. At the cellular level this would attenuate (i) glutathione synthesis; (ii) recycling of oxidised glutathione; (iii) activity of oxidoreductases; and (iv) phase II metabolism inducibility. The effects combined would render the cell and tissue more vulnerable to oxidative stress. Indeed, Nrf2 knock out animals exhibit increased susceptibility to various types of chemical-induced injury. Several studies have shown that OTA exposure can inhibit Nrf2 responses. Such an action would initially lead to increased susceptibility to both physiological and chemical-induced cell stress. However, chronic exposure to OTA may also act as a selective pressure for somatic mutations in Nrf2 or its inhibitor Keap-1, leading to constitutive Nrf2 activation. Nrf2 overexpression confers a survival advantage and is often associated with cancer cell survival. Here we review the evidence for OTA’s role as an Nrf2 inhibitor and discuss the implications of this mechanism in nephrotoxicity and carcinogenicity.

1. Introduction

The ochratoxin family of mycotoxins is found in a wide variety of foods, including cereals, meat, dried fruits, nuts, coffee, wine and beer. Ochratoxin A (OTA) is considered the most toxic of the family and is found at highest concentrations in European food stuffs. The average daily intake of a European adult is estimated at 1 ng.kg⁻¹ b.w., although exposure rates can be up to eight times higher [1,2]. OTA’s main target is the renal proximal tubule where it is taken up from the interstitium via the organic anion transporters (OAT) 1 and 3 and from the lumen via OAT4 [3,4]. While it is also taken up by other tissues, such as the liver, OTA accumulates at higher rates in proximal tubule cells, which is responsible for its renal specificity. OTA is both a nephrotoxin and a renal carcinogen [5]. It has also been shown to cause renal tumors in rats with high metastatic potential [6,7]. Several mechanisms have been proposed for these adverse effects of OTA, including genotoxicity [8], cytoskeleton destabilization [5,9] and histone acetyltransferase (HAT) inhibition [10]. In addition, there is increasing evidence that shows that OTA inhibits the Nrf2 oxidative stress response.

2. The Nrf2 Pathway

The nuclear factor, erythroid 2-like 2 (NFE2L2 or Nrf2) constitutes the main oxidative stress response and drives the transcription of genes involved in glutathione synthesis and recycling, phase II metabolism and the reduction of oxygen species and quinones [11]. Under basal conditions, the Nrf2 protein is sequestered in the cytosol by the actin bound Keap-1 homodimer and targeted for ubiquitination by CUL3, an E3 ubiquitin ligase [11]. Keap-1 contains specific cysteine thiol residues that are sensitive to oxidative and electrophilic stress and, once modified, inhibit Keap-1’s ability to bind Nrf2. Unbound Nrf2, a member of the cap “n” collar (CNC) subfamily of bZIP transcription factors, translocates to the nucleus, heterodimerises with members of the small maf protein family and initiates transcription by binding to antioxidant/electrophilic response elements (ARE/EpRE) [12,13]. The ARE/EpRE is contained within the promoters of several genes including those involved in (i) glutathione synthesis and recycling, comprised of glutamate-cysteine ligase, catalytic and modifier subunits (GCLC, GCLM), glutathione reductase (GSR); (ii) genes with antioxidant properties, such as heme oxygenase 1 (HMOX1), NAD(P)H dehydrogenase, quinone 1 (NQO1), superoxide dismutase 1 (SOD1), thioredoxin reductase 1 (TXNRD1), sulfiredoxin (SRXN1) and aldo-keto reductases (AKRs); and (iii) genes involved in xenobiotic metabolism and transport, comprised of glutathione-S-transferases (GSTs), UDP-glucuronosyltransferase 1A1 (UGT1A1) and ATP-binding cassette, sub-family C3 (ABCC3) [14,15,16,17,18,19]. Since the activation of Nrf2 results in changes in transcription, mRNA profile of the target genes is an ideal method to detect the complete activation of the pathway.

The Nrf2 response has been shown to be robustly induced in several tissues in response to chemical and physiological stressors. For example, many nephrotoxins induce Nrf2 nuclear translocation and Nrf2 dependent gene induction in renal epithelial cells, including potassium bromate, cadmium chloride, diquat dibromide and cyclosporine A [20,21,22]. This pathway has also been shown to be activated in pulmonary models exposed to heavy metals [23,24]. Additionally, we have recently shown that glucose depletion and subsequent re-introduction can result in Nrf2 activation [25]. Thus activation of the Nrf2 pathway provides a robust transcriptional response to redress an increase in oxidative equivalents, protecting the cell from oxidative stress. This is best illustrated in Nrf2 knock-out mice, which are more susceptible to chemically induced toxicity [26,27,28]. For example Nrf2^-/- homozygote mice are far more sensitive to acetaminophen induced hepatotoxicity than wild type or heterozygotes [29].

3. OTA: An Inhibitor of Nrf2?

A number of studies have shown that OTA induces oxidative stress and that pre-incubation of antioxidants can protect against OTA induced injury (reviewed in [30]). For example it has been demonstrated that OTA induces a dose-dependent increase in reactive oxygen species (ROS) in primary rat proximal tubule cells and in the LLC-PK1 cell line, leading to a depletion of intracellular glutathione and cell death [31]. Pre-incubation with the anti-oxidant N-acetylcysteine (NAC) attenuated these effects [31]. However, no study has reported an Nrf2 activation in response to OTA and a large genome-wide transcriptomic study reported there was no induction of Nrf2 dependent genes by OTA in the five different in vitro proximal tubular models tested [5]. This is a rather strange phenomenon for a compound that induces oxidative stress. Thus it is possible that OTA exposure somehow prevents Nrf2 activation. There are several lines of evidence to support this hypothesis.

Rats exposed to OTA by oral gavage for up to one year exhibited a decrease in the mRNA of Nrf2-dependent genes in the kidneys, but not the liver [32]. This presumably reflects the fact that uptake is higher in the kidney and provides direct evidence for OTA acting as an Nrf2 inhibitor. The genes affected included GCLC, GCLM, glutathione synthetase (GSS), UGT3B5 and multiple GST isoforms. Decreases in protein levels were confirmed for GSTP and GCLC by western blot after 21 days and 12 months of exposure to OTA [32]. In an in vitro study we have shown that OTA exposure resulted in an inhibition of Nrf2-dependent genes in human primary proximal tubule cells (Figure 1). Cavin et al. [33] have also demonstrated an OTA-induced Nrf2 inhibition by investigating the protein expression of several Nrf2-regulated genes in rat liver and kidney cell cultures. They showed that OTA depleted both renal and hepatic cells of GSH and decreased the protein levels of Nrf2 targets NQO1, GCLC, GSTA5, GSTP1 and AKR7A1.

Figure 1. Ochratoxin A (OTA) (5 µM) induced an inhibition of Nrf2-dependent genes in human primary proximal tubule cells. Human primary proximal tubular cells from three different donors were cultured to confluence and treated with 5 µM OTA for 1 (grey bar) and 3 days (black bar). RNA was isolated and ran on Affymetrix HGU-133 plus 2 arrays. Nrf2-dependent genes were selected for graphical representation and are expressed as log 2 fold over time-matched (TM) control ± SEM. See [5] for further details.

Figure 1. Ochratoxin A (OTA) (5 µM) induced an inhibition of Nrf2-dependent genes in human primary proximal tubule cells. Human primary proximal tubular cells from three different donors were cultured to confluence and treated with 5 µM OTA for 1 (grey bar) and 3 days (black bar). RNA was isolated and ran on Affymetrix HGU-133 plus 2 arrays. Nrf2-dependent genes were selected for graphical representation and are expressed as log 2 fold over time-matched (TM) control ± SEM. See [5] for further details.

4. Potential Mechanisms of OTA-Induced Nrf2 Inhibition

There are several potential mechanisms for OTA-induced Nrf2 inhibition: (i) inhibition of Nrf2 nuclear translocation; (ii) inhibition of Nrf2 DNA binding; or (iii) epigenetic effects preventing normal Nrf2-dependent transcription.

Independent studies have shown that OTA inhibits Nrf2 activation prior to nuclear translocation [34,35]. Kumar et al. exposed mice to various concentrations of OTA topically for 24 h [34]. They demonstrated a dose-dependent increase in ROS and a concomitant decrease in GSH in skin cells. At the highest concentration, a significant increase in DNA damage was observed. However, there was no nuclear accumulation of Nrf2 at any concentration and even a slight decrease in basal nuclear Nrf2 localization was observed [34]. Ramyaa et al. exposed cultured kidney cells to OTA and also demonstrated a decrease in Nrf2 nuclear translocation compared to control cells [35]. Furthermore they showed that activating Nrf2 by pre-incubation with the flavonoid, quercetin, prevented OTA-induced cell death [35]. In LLC-PK1 cells, Boesch-Saadatmandi et al. demonstrated that co-administration of OTA severely attenuated sulforaphane-induced Nrf2 nuclear translocation and transactivation [36].

It has also been suggested that OTA can interfere with Nrf2 DNA binding. Two independent studies have shown that OTA induces a dose-dependent decrease in Nrf2 activity using ARE-luciferase reporters [33,37]. Also Cavin et al. demonstrated, using an electrophoretic mobility shift assay, that OTA exposure decreases Nrf2 DNA binding in rat hepatocytes [33]. Interestingly, hepatocytes pre-treated with the coffee diterpenes combination of Cafestol and Kahweol, which is a strong inducer of Nrf2 [38], maintained a robust Nrf2 response in the presence of OTA. However, Nrf2 induction was significantly decreased when OTA was co-incubated with the diterpenes. Thus OTA does not interfere with an ongoing Nrf2 response, but does block the initiation of the response. Although, these studies demonstrate that OTA interferes with Nrf2 DNA binding, they do not exclude the possibility of an inhibition of Nrf2 mobilisation.

There is also a growing weight of evidence showing epigenomic effects of OTA. OTA has been shown both to increase histone deacetylase 3 (HDAC3) expression [32] and histone acetyltransferases (HAT) inhibition [10]. It has also been shown that genes governing histone regulation are induced by OTA, including Jumonji domain containing 6 (Jmjd6), which demethylates histones H3 and H4 [5]. Also a number of histone regulating genes are decreased by OTA, including death-associated protein kinase 3 (Dapk3) H3 and H4 kinase, Zinc finger, MYM-type 3 (Zmym3) a proposed member of the histone deacetylase-containing multiprotein complexes and TAF5-like RNA polymerase II, p300/CBP-associated factor (PCAF)-associated factor (Taf5l) [5]. Taf5l is a member of the PCAF complex which promotes histone acetylation [5]. Thus OTA perturbs gene regulation possibly through promotion of histone hypo-acetylation rendering DNA less accessible for binding of transcriptional machinery. Such an effect would negatively affect transcription factor DNA binding, including Nrf2/ARE binding, contributing to a decrease in Nrf2-dependent gene transcription.

In the last number of years, it has been demonstrated that microRNAs (miRNAs) are important post transcriptional regulators and some have also been demonstrated to affect Nrf2 and its downstream targets. OTA has also been shown to induce several miRNAs, with an especially high induction of miR-132 in LLC-PK1 cells [39]. This was associated with a decrease of Nrf2 mRNA [39]. Additionally, it was shown that silencing miR-132 with an antigomir, prevented the decrease of Nrf2 mRNA upon OTA exposure [39]. These results suggest an implication of miRNAs, especially miR-132, in the regulation of the Nrf2 gene itself. Long term OTA induction of miR-132 would lead to a depletion of Nrf2 protein pools which would finally result in a complete Nrf2 block.

OTA can inhibit the activation of the Nrf2 pathway at multiple points, as summarized in Figure 2. One of the key events is the inhibition of Nrf2 mobilization and thus translocation to the nucleus. While, the mechanism for this has not yet been elucidated, it has been shown that OTA binds strongly to actin filaments [40]. This would likely interfere with cytoskeletal dynamics. For example we have shown that OTA strongly induced advillin, a member of the gelsolin superfamily which plays a role in actin remodeling [5]. Since Keap-1 is an actin-bound protein, it is possible that OTA prevents the liberation of Nrf2 from the Keap-1 complex. Alternatively, OTA may itself bind Nrf2 and hold it in the cytosol, mimicking Keap-1’s function. Such an action would prevent Nrf2 nuclear translocation and thus binding to the ARE DNA motif regardless of the amount of oxidative equivalents present. Additionally, OTA has epigenetic effects and inhibits HAT activity while inducing HDACs. This would decrease global transcription, including Nrf2-dependent genes. Finally, OTA has been shown to induce miR-132 which targets Nrf2 mRNA and would thus lead to a decrease in Nrf2 protein pools.

Figure 2. Elucidated mechanisms of OTA induced Nrf2 inhibition.

Figure 2. Elucidated mechanisms of OTA induced Nrf2 inhibition.

In conclusion, OTA-induced inhibition of Nrf2 activation and Nrf2 gene transcription together with OTA-induced Nrf2 protein depletion would render the cell defenseless to physiological and compound-induced oxidative stress. This, coupled with the facts that OTA itself induces oxidative stress, and that Nrf2 induction prior to OTA exposure prevents OTA-induced cell death, provides strong evidence that Nrf2 inhibition is the primary mechanism of OTA’s toxicity. Nrf2 inhibition and subsequent increase in ROS would lead to lipid peroxidation, proteotoxic stress and oxidative DNA damage. Other protective pathways would inevitably be activated, such as p53, to prevent the cell replicating by initiating cell cycle blockade and promoting apoptosis. However, over a chronic time course such a situation will create a selective pressure leading to escape from p53 activity and thus promotion of a cancerous phenotype. Additionally, Nrf2 inhibition alone may select for cells with somatic mutations in Nrf2 or Keap-1, leading to a constitutive activation of the pathway. A cell without p53 control and a constitutively active Nrf2 system would have a massive survival advantage and would also be very resistant to chemotherapeutics. Indeed, utilizing the high Nrf2 expression in tumor cells is now being considered as a method for tumor specific targeting of toxic payloads [41]. In conclusion, there is compelling evidence that OTA’s inhibition of Nrf2 is the mechanism for both its nephrotoxicity and carcinogenicity.