Aryl Hydrocarbon Receptor-Dependent and -Independent Pathways Mediate Curcumin Anti-Aging Effects

The aryl hydrocarbon receptor (AhR) is a ligand-activated transcription factor whose activity can be modulated by polyphenols, such as curcumin. AhR and curcumin have evolutionarily conserved effects on aging. Here, we investigated whether and how the AhR mediates the anti-aging effects of curcumin across species. Using a combination of in vivo, in vitro, and in silico analyses, we demonstrated that curcumin has AhR-dependent or -independent effects in a context-specific manner. We found that in Caenorhabditis elegans, AhR mediates curcumin-induced lifespan extension, most likely through a ligand-independent inhibitory mechanism related to its antioxidant activity. Curcumin also showed AhR-independent anti-aging activities, such as protection against aggregation-prone proteins and oxidative stress in C. elegans and promotion of the migratory capacity of human primary endothelial cells. These AhR-independent effects are largely mediated by the Nrf2/SKN-1 pathway.


Introduction
The aryl hydrocarbon receptor (AhR) is a ubiquitous ligand-activated transcription factor identified as a determinant for the toxicological response to 2,3,7,8-tetrachlorodibenzop-dioxin (TCDD) in mammals [1]. AhR signaling pathways have been well described in mammalian cells. Briefly, unliganded AhR is localized in the cytoplasm and stabilized by diverse co-factors, such as 90-kDa heat shock protein (Hsp90), the AHR-interacting protein (AIP), and the chaperone p23. Binding to exogenous (e.g., TCDD) or endogenous (e.g., kynurenine) ligands promotes the translocation of this complex into the nucleus,

Gene Silencing by RNA-Mediated Interference (RNAi)
Gene silencing was achieved through feeding E. coli HT115(DE3) expressing plasmids with dsRNA against specific genes [50]. RNAi feeding was applied continuously from birth to death. For juglone resistance assay with HT115(skn-1) bacteria, RNAi feeding was applied from L4 worms for 24 h before transferring them to fresh juglone plates.

Lifespan
The lifespan analysis was started from a synchronized population of worms, which was transferred to fresh NGM plates daily during the fertile period. After the fertile phase, the animals were transferred every alternate day. Dead, alive, and censored animals were scored during the transferring process. Animals were counted as dead when they showed neither movement, nor response to a manual stimulus with a platinum wire, nor pharyngeal pumping activity. Animals with internal hatching (bags), an exploded vulva, or which died desiccated on the wall were censored. The number of dead and censored animals was used for survival analysis in OASIS [52] or OASIS 2 [53]. For the calculation of the mean lifespan and the survival curve in OASIS and OASIS 2, the Kaplan-Meier estimator was used, and the p-values were calculated using the log-rank test between pooled populations of animals. The movement was set as a parameter for healthy aging, and the phase of the active movement is referred to as health span. It was assessed in the populations used for the lifespan assay. Animals, which were either crawling spontaneously or after a manual stimulus, were considered as moving, while dead animals or animals without crawling behavior were considered as not moving. Statistical analysis was done as described for lifespan.
2.1.6. Curcumin Treatment of C. elegans Curcumin (Sigma Aldrich, Taufkirchen, Germany) was dissolved in DMSO (Carl Roth, Karlsruhe, Germany) in a concentration of 100 mM and supplied to the NGM after autoclaving. The final concentration of curcumin in the media was 100 µM (0.1% DMSO). Control plates contained 0.1% DMSO. Worms were treated continuously starting from eggs.

Quantification of PolyQ Aggregates
PolyQ 40 aggregates were visualized by fluorescence microscopy (100× magnification) in 10-day-old worms anesthetized with 15 mM sodium azide (Sigma Aldrich, Taufkirchen, Germany). To assess the number of aggregates, images were stitched using the Fiji pairwise stitching plugin [54] to create whole worms, and the number of the aggregates was quantified in Fiji [55] using the plugin "Analyze Particles".

Quantification of α-Synuclein Aggregates
α-synuclein aggregates in the head muscles of 7-day-old worms were visualized by fluorescence microscopy (400× magnification) in worms anesthetized with 15 mM sodium azide (Sigma Aldrich, Taufkirchen, Germany, S2002). Pictures were segmented using Ilastik (version 1.3.0) (Laboratory of Anna Kreshuk at the European Molecular Biology Laboratory, Heidelberg, Germany) (available on https://www.ilastik.org/, accessed on 10 April 2018) [56]. The segmented pictures were used to analyze the number of aggregates in Fiji [55] using the plugin "Analyze Particles".

Microarray and GO Term Analysis
Samples from five independent replicates with approximately 1000 3-day-old worms per condition were collected, and the RNA was extracted and loaded to an Affymetrix Chip. The microarray raw data in the format of CEL were analyzed using the software R (version 3.4.2) (R Foundation, Vienna, Austria) and Bioconductor (The Bioconductor Project, Bioconductor is open source and open development) [57]. Background correction, normalization, and expression calculation were performed with the oligo package [58] and the RMA method. For quality control of the array, the package arrayQualityMetrics_3.34.0 [59] was used. Because of the quality measures, sample ahr-1C5 was excluded from further analysis. The differentially expressed genes were identified using the limma package and a linear model and moderated t-statistic with FDR to test for multiple comparisons [60]. A p-value of 0.1 was applied. The differentially expressed genes were analyzed for Gene Ontology term enrichment using Cytoscape (version 3.6.0) (The Cytoscape Consortium, an independent not-for-profit organization) [61] with the plugin ClueGo (version 2.5.0) (Laboratory of Integrative Cancer Immunology, Paris, France) [62]. The microarray data can be accessed through the Gene Expression Omnibus accession no. GSE195769.

ROS Quantification
MtROS were detected in live wt and ahr-1 mutants worms using MitoSOX Red (Ther-moFisher Scientific, Dreieich, Germany). Nematodes were synchronized by egg laying onto IPTG plates using HT115(L4440) bacteria as food. Then, 48 h later, 50 animals at the L4 stage were transferred onto freshly prepared 10 µM MitoSOX Red plates seeded with UV-killed HT115(L4440). The worms were incubated in the dark at 20 • C. Following 16 h incubation, they were moved onto new NGM plates spread with live HT115(L4440) for 1 h to remove residual dye from the intestines. For imaging, nematodes were mounted onto Antioxidants 2022, 11, 613 5 of 30 2% agarose pad slides, anesthetized by adding 10 mM levamisole and fixed by ProLong™ Glass Antifade Mountant (ThermoFisher Scientific, Dreieich, Germany). Images were acquired immediately with a Zeiss Axio Imager M1 microscope (Carl Zeiss, Inc., Cologne, Germany) using a 40× objective and a DsRed Filter. Afterward, the worm head region was manually selected, and the integrated intensity was calculated using the imaging software Fiji [55].

Tetramethylrhodamine Ethyl Ester (TMRE) Assay
To assess the mitochondrial membrane potential, nematodes were synchronized by egg laying on IPTG plates seeded with HT115(L4440) bacteria. On the day of the experiment, TMRE (Invitrogen, Eugene, OR, USA) was dissolved in DMSO to a concentration of 5 mM and then diluted to 30 µM with heat-inactivated HT115(L4440) (30 min, 65 • C). A total of 150 µL of this solution was added per plate and left to dry in the dark for approximately 30 min. Sixty adult synchronous worms at 1, 3, or 5 days of adulthood were picked onto the TMRE plates prepared and left to the stain to absorb for 2 h in the dark at 20 • C. After staining, worms were transferred onto IPTG plates seeded with heatinactivated HT115(L4440) and incubated for 1 h in the dark at 20 • C, to remove residual dye from the intestines. For imaging, 10 nematodes were mounted onto 2% agarose pad slides, anesthetized by adding 10 mM levamisole, and fixed by ProLong™ Glass Antifade Mountant (ThermoFisher Scientific, Dreieich, Germany). For each experimental run, 5 slides were prepared per group. Images were acquired immediately with a Zeiss Axio Imager M1 microscope (Carl Zeiss, Cologne, Germany) using a 2.5× objective and a DsRed filter. The fluorescence intensity was calculated using Fiji [55].

Pharyngeal Pumping Rate and Motility Assay
N2 and CZ2485 nematodes were synchronized by bleaching [63] and the eggs were left to hatch in egg buffer (118 mM NaCl, 48 mM KCl, 2 mM CaCl 2 , 2 mM MgCl 2 , 25 mM Hepes, pH 7.3) overnight, on orbital shacking. L1 larvae were spotted onto NGM supplemented with 1 mM IPTG and containing 0.1% DMSO or 100 µM curcumin. HT115(L4440) bacteria were used as food. Young adult worms were collected with M9 buffer, centrifuged (300g × 3 min), and washed twice to remove bacteria. Worms were incubated with 0-1 mM H 2 O 2 (Sigma-Aldrich, Taufkirchen, Germany) (100 worms/100 µL), for 2 h on orbital shaking. Control worms were incubated with M9 buffer only. After 2 h, worms were moved onto NGM supplemented with 1 mM IPTG and containing 0.1% DMSO or 100 µM curcumin and seeded with HT115(L4440) bacteria as food. The pharyngeal pumping rate, scored by counting the number of times the terminal bulb of the pharynx contracted over a 1 min interval (pumps/min), and the motility assay, scored by counting the number of body thrash (body bends/min) in M9 buffer over a 1 min interval, were scored from 2 up to 20 h later.
2.1.13. Acute Juglone Sensitivity Assay N2 and CZ2485 nematodes were synchronized by egg laying onto NGM plates with either DMSO or 100 µM of curcumin. Plates were supplemented with 1 mM IPTG and seeded with HT115(L4440) or HT115(ugt-45) bacteria as food. To evaluate the effect of skn-1 RNAi, the worms were synchronized by egg laying onto DMSO or curcumin plates seeded with HT115(L4440) bacteria. As nematodes reached the L4 larval stage, they were transferred for 24 h onto DMSO or curcumin plates seeded with HT115(skn-1) bacteria. Day 1 adult worms (25 worms) were moved onto fresh NGM plates containing 200 µM Juglone (Merck, Darmstadt, Germany) and seeded with 25 µL of 10× concentrated bacteria overnight culture. Worm survival under juglone-induced oxidative stress was checked by touch-provoked movement hourly, for 6 h. Animals were scored as dead when they failed to respond to touch with a platinum wire pick. Nematodes desiccated on the wall were censored. The number of dead and censored animals was scored and the Online Application for Survival analysis OASIS 2 was employed for survival analysis [53].
2.1.14. Quantification of the gst-4::GFP Intensity NV35wt and NV35a were synchronized by egg laying onto NGM plates supplemented with 1 mM IPTG and containing 0.1% DMSO or 100 µM curcumin. HT115(L4440), HT115(ugt-45) and HT115(skn-1) bacteria were used as food. To visualize GFP fluorescence, day 1 adult worms were anesthetized with 10 mM levamisole hydrochloride solution and mounted on 2% agarose pads. Images were immediately acquired with a Zeiss Axio Imager M1 microscope (Carl Zeiss, Cologne, Germany), 2.5× magnification) and then analyzed using the software CellProfiler (The CellProfiler project team, Cimini Lab at the Broad Institute of MIT and Harvard, MA, USA). Briefly, images were processed using a pipeline to segment worms in each image from bright field microscopy and separate them from the background. Then, the integrated GFP intensity was measured per worm.
Samples from 3 independent replicates with approximately 1000 3-day-old worms per condition were collected and RNA was extracted. After washing and elution, the RNA content was quantified by spectrophotometry, and 1-2 µg of RNA was used for the cDNA synthesis (Omniscript RT Kit (Qiagen, Hilden, Germany). Primer pairs are listed in Table S1. For the Real-time qPCR, the cDNA was diluted at 1:20 in 10 mM TRIS (pH 8.0). For the reaction, the qPCR Green Core kit (Jena Biosciences, Jena, Germany)) or the GoTaq ® qPCR kit (Promega, Walldorf, Germany) was used. The samples were run in a MyiQ2 cycler (BioRad, Feldkirchen, Germany), and the expression of each sample was measured in duplicate on the same multi-well plate. The expression was calculated relative to the reference genes act-1 and cdc-42 using the iQ5 software. All data collected were enabled for gene study according to the BioRad user instructions, and the expression was calculated using the normalized expression (ddC T ). The efficiency of each primer pair reaction was added for the correct quantification of the normalized expression. The efficiency was assessed with 1:20, 1:100, 1:500, and 1:2500 dilutions of the cDNA. From normalized expression values, the fold-change compared to wild-type was calculated for each replicate.

Treatment of Cos7 Cells
Stock solutions at concentrations 1000-times higher than the desired treatment concentration were prepared for all of the compounds. Curcumin (Sigma Aldrich, Taufkirchen, Germany), Benzo(a)pyrene (Sigma Aldrich, Taufkirchen, Germany), leflunomide (Sigma Aldrich, Taufkirchen, Germany), and lutein (Sigma Aldrich, Taufkirchen, Germany), were dissolved in DMSO (Carl Roth, Karlsruhe, Germany), while resveratrol (Sigma Aldrich, Taufkirchen, Germany) and rotenone (Sigma Aldrich, Taufkirchen, Germany) were dissolved in ethanol (Carl Roth, Karlsruhe, Germany). At 24 h after transfection, the cell culture medium of the cells was replaced with a cell culture medium containing a 1:1000 dilution of the respective compound. The cells were treated for 24 h before assessing the luciferase activity.

Luciferase Assay (AhR Activity)
The AhR transcriptional activity was assessed by measuring the activity of an XREdriven luciferase [64]. For this, a Dual-Luciferase Reporter Assay System (Promega, Walldorf, Germany) was used. After a 24 h treatment, Cos7 cells were washed twice with PBS and then lysed for 15 min at RT using the passive lysis buffer included in the Dual-Luciferase Reporter Assay kit. A total of 20 µL of the lysed cells were placed in a white 96-well plate and used for luminescence measurements. The luciferin (LARII) and renilla (Stop&Glo) substrates were prepared according to the manufacturer's description. The samples were loaded on a luminometer (EG&G Berthold microplate Luminometer LB 96V Microluminomat plus (Berthold Technologies, Bad Wildbad, Germany) and the substrates were attached to the tubing system of the luminometer. First, 65 µL of LARII was added to each well of the sample, and the luminescence produced by the firefly luciferase was measured, then 65 µL of Stop&Glo reagent was added and the luminescence produced by the Renilla luciferase was measured. To assess AhR activity from the luminescence measurements, we performed the following post-processing steps: First, the luminescence of non-transfected cells was subtracted from the luminescence of each sample for background correction. In the next step, we normalized the luciferase luminescence to the renilla luminescence of the same sample to eliminate differences in the transfection rate and cell number. Another normalization step to the pcDNA-VP16 transfected cells was performed for each treatment group to remove AhR-independent effects on the XRE-driven luciferase.

Transient Transfection of EC
Cells were transfected as described previously [65]. In brief, EC were transfected by using SuperFect ® Transfection Reagent (Qiagen, Hilden, Germany) according to the manufacturer's instructions. The overexpression or knockdown of AhR was achieved after 24 or 48 h, respectively. The transfection efficiency upon overexpression was approximately 40%.

Scratch Wound Assay of EC
For investigation of the migratory capacity of EC, scratch wound assays were performed as described previously [66]. In detail, wounds were set into a cell monolayer with a cell scraper along a trace line. After the injury, non-attached cells were removed by gentle washing. The curcumin treatment was performed directly after the wound was set. Curcumin was dissolved in DMSO and used at the final concentration of 7.5 µM. EC migration was quantified by staining the cells with 5 µg/mL 4 , 6-diamidino-2-phenylindole (DAPI) (Carl Roth, Karlsruhe, Germany) in PBS for 5 min after the cells had been fixed with 4% (v/v) paraformaldehyde for 15 min at room temperature. Images were taken using a Zeiss AxioVision Observer D1 fluorescent microscope (Carl Zeiss, Oberkochen, Germany)) using a 200-x magnification. Cells migrated into the wound from the trace line were automatically counted using the particle analysis function of ImageJ 1.52a [67] after overlapping nuclei were separated.

qPCR in Cells
The total cellular RNA was isolated by combining lysis in TRIzol™ with downstream processing using the RNeasy Mini Kit (Qiagen (Hilden, Germany)) according to the manufacturer's instructions. cDNA synthesis was performed using the QuantiTect ® Reverse Transcription Kit (Qiagen (Hilden, Germany)) with 1 µg RNA according to the manufacturer s instructions. Relative transcript levels were determined by pPCR using the 2x SYBR ® Green qPCR Master Mix and a Rotor-Gene ® Q thermal cycler (Qiagen (Hilden, Germany)). The transcript for the ribosomal protein L32 (rpl32) was used as a reference, and the relative expression was calculated by the ∆C t -method [68]. The following intron-spanning primer pairs were used: cyp1a1 (gene accession number NM_000499.

qPCR in Mice
Total RNA was isolated from organ tissues of three WT and three AHR deficient mice with TriZol ® . Then 400 ng of RNA was reverse transcribed using the reverse transcriptase M-MLV (Promega, Madison, WI, USA) and random hexamer primers. Gene expression levels were measured in duplicate for each mouse tissue on a Rotor-Gene Q (Qiagen, Hilden, Germany), in 15 µL final volume, containing 7.5 µL Rotor Gene SybrGreen™ (Biorad, Feldkirchen, Germany), 1 µM of each primer, 1.5 µL cDNA and RNase free water. Primer efficiencies were between 90% and 146%. See Table S2 for primer sequences and efficiencies. Expression levels were calibrated to the expression of RPS6 as a house-keeping gene in the same sample using the 2 −∆∆CT method [69].

In Silico Analyses
Homology Modeling of the CeAhR LBD The structural model of C. elegans AhR LBD (residues 267-372) was generated by homology modeling. The X-ray structures of the PASB domains of homologous bHLH-PAS family members sharing the highest sequence identity (about 20%) with the CeAhR PASB were used as templates: the circadian locomotor output cycles kaput (CLOCK, PDB: 4F3L), the neuronal PAS domain-containing protein 3 (NPAS3, PDB: 5SY7), the Hypoxia-inducible factors 2α (HIF2α, PDB: 3H82, 4ZP4, 3F1N) and 1α (HIF1α, PDB: 4H6J). The model was obtained with MODELLER [70][71][72]. The optimal model was selected from among the 100 generated, based on the best DOPE SCORE [73]. The quality of the models was evaluated using PROCHECK [74]. Secondary structures were attributed by DSSPcont [75]. The binding cavity within the modeled LBDs was characterized using the CASTp server [76]. Visualization of the models was accomplished using PYMOL [77].

Statistical Analysis
Unless otherwise stated, statistical analyses were performed in GraphPad Prism (Version 6.01) (GraphPad Software, Inc. San Diego, CA, USA). For life/health span assays, statistical analysis was done using OASIS [53]. Statistical analysis of the microarray data was performed in R (R Foundation (Vienna, Austria)). Boxplots were created in GraphPad Prism (Version 6.01) (GraphPad Software, Inc. San Diego, CA, USA) and show the median (line), 25-75th percentile (box) and 10-90th percentile (whiskers).

Curcumin Promotes Health Span in an AhR-Dependent and -Independent Manner
Loss of ahr-1 promotes C. elegans' health-and lifespan in basal conditions [14] and it negatively impacts age-related traits in response to mammalian AhR modulators, such as benzo[a]pyrene (BaP), UVB light, and microbiota [25]. Dietary polyphenols, such as curcumin, form an important group of mammalian AhR modulators with pro-longevity effects in C. elegans [78,79] and we thus investigated the lifespan-extending effect of curcumin for its ahr-1 dependency. Curcumin reproducibly and significantly extended the life-and health spans of C. elegans in an ahr-1-dependent manner ( Figure 1A,B). Previously, we have shown that loss of ahr-1 also extends the lifespan in Huntington's disease and Parkinson's disease models, with muscle-overexpression of aggregation-prone polyglutamine (polyQ40) and α-synuclein (α-syn), respectively, while at the same time increasing their content of protein aggregates [25]. Interestingly, curcumin treatment increased the number of polyQ40 and α-syn aggregates to the same extent as ahr-1 loss of function ( Figure 1C). Curcumin also promoted lifespan and locomotory ability in these disease models ( Figure 1D,E), but the effects of ahr-1 loss and curcumin supplementation were additive in the PolyQ background ( Figure 1D), revealing AHR-1-independent protective functions of curcumin at least in this compromised background.
fects in C. elegans [78,79] and we thus investigated the lifespan-extending effect of curcumin for its ahr-1 dependency. Curcumin reproducibly and significantly extended the lifeand health spans of C. elegans in an ahr-1-dependent manner ( Figure 1A,B). Previously, we have shown that loss of ahr-1 also extends the lifespan in Huntington's disease and Parkinson's disease models, with muscle-overexpression of aggregation-prone polyglutamine (polyQ40) and α-synuclein (α-syn), respectively, while at the same time increasing their content of protein aggregates [25]. Interestingly, curcumin treatment increased the number of polyQ40 and α-syn aggregates to the same extent as ahr-1 loss of function (Figure 1C). Curcumin also promoted lifespan and locomotory ability in these disease models ( Figure 1D,E), but the effects of ahr-1 loss and curcumin supplementation were additive in the PolyQ background ( Figure 1D), revealing AHR-1-independent protective functions of curcumin at least in this compromised background.

ugt-45 Mediates the Anti-Aging Effects of Curcumin and ahr-1 Depletion
In search of possible downstream ahr-1-dependent effectors of curcumin, we took targeted and unbiased approaches. We examined the expression of classical mammalian AhR target genes and focused on the Cyp genes since curcumin alters Cyp1A1 and Cyp1B1 expression in mammalian cells [80,81]. However, the quantification of 47 different cyps in C. elegans by semi-quantitative real-time PCR (qPCR) revealed that only cyp-13B1 was significantly up-regulated either by ahr-1 depletion or by curcumin in an ahr-1-dependent manner ( Figure S1A-B), while the three other cyps (i.e., cyp-13A5, cyp-13A8 and cyp-42A1) were increased by curcumin only in the absence of ahr-1 ( Figure S1). These data, along with other works [25,82], suggest that cyps are likely not the major targets of CeAhR. This is also supported by our transcriptomic analysis in wild-type and ahr-1 mutants. Indeed, consistent with the role of AHR-1 in neuronal determination [37,38,40,41], the gene expression changes between wild-type and ahr-1 mutants showed enrichment in processes linked to neuronal development and differentiation and no major changes in classical detoxification genes (Figure 2A). qPCR analysis of some of the most up-and down-regulated genes between ahr-1(ju145) and wild-type (atf-2, K04H4.2, egl-46, T20F5.4, ptr-4, dyf-7, clec-209, C01B4.6, C01B4.7, F56A4.3) mostly confirmed their ahr-1-dependency in basal conditions ( Figure 2B) but neither UVB [25] nor curcumin ( Figure 2C) significantly affected the expression of these genes. We wondered whether the expression changes in these genes are evolutionarily conserved and assessed their expression in different tissues (i.e., brain, liver, gut, and blood) of 8-and 18-month-old wild-type and AhR KO mice. Some genes showed a tendency for an increased expression in young (atf-2 homolog) or old (lpr-4/5 homologs) mice in a tissue-specific manner, but neither an obvious pattern nor conserved changes were observed ( Figure S2). These results reflect possible species-specific differences or tissue-dependent AhR transcriptional activity in mammals overlooked by whole-animal transcriptomic analysis in C. elegans.
A thorough examination of the most differentially expressed genes between C. elegans wild-type and ahr-1(ju145) revealed that the expression of many of these genes is affected in C. elegans during aging and by dietary mammalian AhR modulators (e.g., quercetin and resveratrol) [25], thus suggesting a role for AHR-1 in polyphenol-modulated gene expression. In line with this scenario, the microarray data showed that most of the genes differentially expressed upon curcumin treatment were indeed regulated in an ahr-1-dependent manner ( Figure 2D; Table 1). Out of 47 genes altered by curcumin in the wild-type (43 upand 4 down-regulated), only 5 were also induced by curcumin in ahr-1(ju145). Among the genes regulated by curcumin in an AHR-1-dependent manner were phase II enzymes and interestingly, some of them (ugt-9 and ugt-29), were regulated in the same direction by curcumin or by loss of ahr-1 (Table 1). Thus, we checked their expression and that of additional ugts (ugt-45 and ugt-57) that were differentially expressed when applying a less restrictive statistical analysis not corrected for multiple comparisons. Of the examined genes, ugt-45 was increased in ahr-1(ju145) and by curcumin treatment (Figure 3A,B). We also observed changes in the expression of some detoxification genes between wild-type and AhR KO mice in a tissue-dependent manner. The differential expression of those genes was highest in the brain, where Ugt2a3 (ugt-9 and ugt-29 in C. elegans) was down-and Hpgds (gst-4 in C. elegans) was up-regulated ( Figure S3A). There was no change in the expression of any of the tested genes in the liver samples of mice ( Figure S3B). In line with the C. elegans data, the ugt-45 murine homolog Ugt3a2 showed a tendency toward overexpression in the intestines of Ahr KO mice ( Figure S3C). Notably, ugt-45 RNAi prevented the beneficial effects on lifeand health spans promoted by curcumin ( Figure 3C,D) or ahr-1 depletion ( Figure 3E,F) indicating that the two interventions may rely on jointly modulated downstream signaling to elicit their anti-aging activity.
change in the expression of any of the tested genes in the liver samples of mice ( Figure  S3B). In line with the C. elegans data, the ugt-45 murine homolog Ugt3a2 showed a tendency toward overexpression in the intestines of Ahr KO mice ( Figure S3C). Notably, ugt-45 RNAi prevented the beneficial effects on life-and health spans promoted by curcumin ( Figure 3C,D) or ahr-1 depletion ( Figure 3E,F) indicating that the two interventions may rely on jointly modulated downstream signaling to elicit their anti-aging activity. diagram of differentially expressed genes on the microarray. The number of genes that were differentially up-or down-regulated between the indicated conditions is shown in red and blue, respectively. The numbers in the interchanges refer to the genes that occurred in both comparisons. The values in the lower right corner show the number of genes on the array that were not differentially expressed.

AHR-1 and Curcumin Independently Protect Against Oxidative Stress
The beneficial properties of polyphenols are often ascribed to their ability to protect against reactive oxygen species (ROS) [83,84]. Since AhR is involved in oxidative stressmediated processes [85][86][87], we wondered whether curcumin may impact animals' physiology via AhR-regulated antioxidant responses. We observed that ahr-1 mutants produce more mitochondrial(mt)ROS and have a reduced mitochondrial membrane potential (Figure 4A,B), two parameters correlating with longevity [88,89]. While consistent with the mitohormesis paradigm ahr-1(ju145) produce slightly more mtROS and live longer, these animals were more sensitive to oxidative stress than the wild type. Specifically, the detrimental effects induced by juglone and H2O2 on the animals' pumping, motility and

AHR-1 and Curcumin Independently Protect against Oxidative Stress
The beneficial properties of polyphenols are often ascribed to their ability to protect against reactive oxygen species (ROS) [83,84]. Since AhR is involved in oxidative stress-mediated processes [85][86][87], we wondered whether curcumin may impact animals' physiology via AhR-regulated antioxidant responses. We observed that ahr-1 mutants produce more mitochondrial(mt)ROS and have a reduced mitochondrial membrane potential ( Figure 4A,B), two parameters correlating with longevity [88,89]. While consistent with the mitohormesis paradigm ahr-1(ju145) produce slightly more mtROS and live longer, these animals were more sensitive to oxidative stress than the wild type. Specifically, the detrimental effects induced by juglone and H 2 O 2 on the animals' pumping, motility and survival were significantly stronger in ahr-1(ju145) compared to the wild type ( Figure 4C-F). These data suggest that AHR-1 depletion has beneficial mitohormetic effects in basal conditions, while its presence is required for oxidative stress protection, thus uncoupling two often correlating age-related parameters, namely lifespan and stress resistance. Instead, curcumin significantly improved H 2 O 2 and juglone resistance in both wild-type and ahr-1 mutants ( Figure 4E,F), suggesting that curcumin elicits an ahr-1-independent antioxidant response. Consistent with the uncoupled regulation of lifespan and oxidative stress resistance, ugt-45 silencing did not affect sensitivity to oxidative stress either for ahr-1 mutants or curcumin-treated animals ( Figure 4G). Thus, curcumin has pro-longevity effects via ahr-1 and ugt-45, but protects against oxidative stress through ahr-1-independent mechanisms.

Nrf2/SKN-1 Mediates the AhR-Independent Effects of Curcumin
To further evaluate AhR-curcumin crosstalk in additional age-related features, we measured the migratory capacity in human primary EC-a hallmark for vessel functionality, which declines with age [90] and is reduced by AhR activation [14]. In line with the anti-aging activity of ahr-1 suppression and of curcumin, AhR overexpression significantly inhibited, while curcumin increased, the migratory capacity of primary human EC ( Figure 5A). Of note, the induction of migratory ability by curcumin was comparable in empty vector-or AhR expression vector-transfected cells ( Figure 5A). However, the migration of curcumin-treated cells was significantly reduced by AhR overexpression: curcumin induces in empty vector-transfected cells up to 60 migrated cells per high power field, while in AhR overexpressing cells only up to 25 cells per high power field ( Figure 5A). These data suggest that the pro-migratory effect of curcumin is modulated by AhR-independent mechanisms but possibly also by a reduction in AhR activity. We next determined intracellular AhR distribution and the expression of cyp1a1 in curcumin-treated human EC. Curcumin did not affect AhR-nuclear translocation ( Figure 5B) or cyp1a1 expression ( Figure 5C).
In search of pathways modulated by curcumin in an AhR-independent manner, we turned back to nematode transcriptomic profiles to find transcription factors regulating genes significantly modulated by loss of ahr-1 or by curcumin treatment in wild-type animals ( Table 1). This in silico search identified the redox transcription factor SKN-1, the ortholog of human Nrf2 (nuclear factor erythroid 2-related factor 2), whose activation by curcumin [91] is often reported as a possible mediator of its anti-oxidant activity [92,93]. Accordingly, the prototype C. elegans Nrf2/SKN-1-dependent gene, gst-4, is overexpressed in the ahr-1 mutant [25] and induced by curcumin in wild-type and even more in ahr-1 mutants ( Figure 5D). Moreover, curcumin increased stabilization and nuclear translocation of Nrf2 in primary human EC ( Figure 5E) and induced the expression of manganese superoxide dismutase (Sod2)-a classic Nrf2 target gene-in the cells transfected with an empty vector or in cells in which AhR is silenced by shRNA ( Figure 5F). The lack of Sod2 induction by AhR shRNA in EC may be due to a partial reduction (50%) in AhR expression ( Figure S3D), which may not be sufficient to trigger the activation of Nrf2 or of additional transcription factor (TF), which, in C. elegans, might concur to the induction of the gst-4 [94] upon complete AhR depletion. Interestingly, Hpgds, a homolog of C. elegans gst-4, was significantly increased in the brain of AhR KO mice ( Figure S3A) but it is not a target of Nrf2. Further evidence for possible Nrf2/SKN-1 independent signaling activated by ahr-1 depletion is that the activation of the gst-4 by curcumin is completely suppressed by skn-1 RNAi in the C. elegans wild type, whereas ahr-1 mutants still induce gst-4 despite skn-1 depletion ( Figure 5G,H). However, skn-1 RNAi reduced oxidative stress resistance in both wild-type and ahr-1(ju145) ( Figure 5I). Unexpectedly, skn-1 silencing did not affect the juglone resistance of curcumin-treated animals ( Figure 5I). Our data reveal a complex scenario whereby curcumin promotes different anti-aging features relying either on AhRdependent or AhR-independent but Nrf2/SKN-1-dependent (and additional) signaling.
ahr-1 mutants ( Figure 4E,F), suggesting that curcumin elicits an ahr-1-independent antioxidant response. Consistent with the uncoupled regulation of lifespan and oxidative stress resistance, ugt-45 silencing did not affect sensitivity to oxidative stress either for ahr-1 mutants or curcumin-treated animals ( Figure 4G). Thus, curcumin has pro-longevity effects via ahr-1 and ugt-45, but protects against oxidative stress through ahr-1-independent mechanisms.

Curcumin and Pro-Oxidants Display Opposite Effects on AHR-1 Activity
Consistent with the anti-aging effect of reduced AhR expression/activity, our data suggest that curcumin may extend the lifespan of C. elegans by suppressing AHR-1-regulated pathways through reduction of AHR-1 expression/activity or acting on common downstream signaling pathways. Hence, we tried to quantify AHR-1 activity in C. elegans, but numerous attempts to evaluate AHR-1 expression and subcellular localization using antibodies (against mammalian AhR or customized antibodies against CeAhR) or fluorescently tagged reporters (OP562, UL1709, ZG93) did not give meaningful evidence. Considering that AHR-1 binds to XREs in vitro [35], we thought to use XRE-driven gene expression as a readout for AHR-1 activity. Thus, we turned to monkey-derived Cos7 cells, which do not express endogenous AhR and thus display no endogenous AhR activity [95,96] and can be exploited to monitor XRE-driven Luciferase induction as a readout for AHR-1 activity (Larigot et al.; submitted along with this study). When Cos7 cells were co-transfected with vectors expressing C. elegans AhR/ahr-1, ARNT/aha-1, and a luciferase-coupled XREcontaining promoter of the human CYP1A1 gene [64] AHR-1 showed low activity in basal (vehicle-treated) conditions. Of note, treatment with curcumin or other nutraceuticals that promote healthy aging in C. elegans, such as lutein [97] and resveratrol [98,99], significantly suppressed AHR-1 activity ( Figure 6A-C). Instead, BaP and leflunomide, known AhR activators in mammals, did not affect AHR-1 activity ( Figure 6A,B) at the concentrations we used. Notably, AHR-1 activity was abolished in Cos7 cells transfected with a vector expressing the ahr-1(ju145) allele instead of the wild-type allele ( Figure 6A-C), suggesting that ju145 is a true loss-of-function allele and that the measured luciferase intensity is due to functional AHR-1.
We then sought to investigate whether curcumin reduces the activity of AHR-1 by direct binding or indirect modulation. To date, no ligands of C. elegans AHR-1 have been identified, and since there is no available information on its LBD, we performed an in silico analysis to characterize it. The two AHR-1 isoforms, 1a and 1b, were aligned and although different in length, their PASB domain sequence is identical. This sequence was then aligned to the PASB domain of Drosophila melanogaster, and to those of two AhRs from vertebrates for which structural models were previously generated, namely mouse (Mus musculus) [100], and zebrafish (Danio rerio) [101] ( Figure 6D). The alignment showed clear differences between species with the main peculiarity of invertebrates baring sequence deletions in the most variable region in the PAS domain, corresponding to the flexible Antioxidants 2022, 11, 613 20 of 30 region, including the helical bundle (Cα, Dα, Eα helices) and the short loops connecting these elements ( Figure 6D,E). These deletions could reduce the available space in the binding cavity of these AhRs. We then generated a 3D model of the AHR-1 PASB by homology modeling. This model presents the typical PAS fold, but with a shorter Dα helix compared to other AhRs. However, the internal cavity has some peculiarities; it contains more hydrophobic residues and is truncated in half by some internal side chains. In particular, H365 and H274 are faced and could form a hydrogen bond in the middle of the cavity; moreover, the Y332, L363, and L302 side chains could obstruct the cavity, reducing the internal space available for ligands ( Figure 6E). This small and truncated cavity most likely does not allow the binding of large ligands (e.g., TCDD or curcumin). Similar to the AHR-1 structural model, a model of the zebrafish zfAhR1a showed that the LBD cavity is truncated compared to the TCDD-binding paralogs zfAhR1b and zfAhR2 [101]. Small and flexible ligands, such as leflunomide, bind and activate the zfAhR1a, but the leflunomide concentration we tested did not activate AHR-1 in our Cos7 cell system ( Figure 6B).
We then wondered whether mutations in amino acids responsible for the small cavity of the LBD might allow classical ligands to activate CeAhR. The CeAhR L363 residue ( Figure 6D) corresponds to A375 in mAhR b−1 and V375 in mAhR d , and this residue has a major impact on ligand binding [102]. Similarly, T386 of zfAhR1a ( Figure 6D), matching to A375 in mAhR b−1 and A386 in zfAhR1b and zfAhR2, contributes to the lack of TCDD binding of zfAhR1a and, when mutated to alanine, restores TCDD sensitivity when Y296H is also introduced [101]. The amino acid Y296 is already a histidine in C. elegans (H274). Thus, we mutated only the leucine at the position L363 in the CeAhR vector to an alanine (L363A) ( Figure 6D,E indicated by an arrow). Moreover, we mutated the nearby histidine at position H365 to glutamine (H365Q), which is Q377 in mice ( Figure 6D,E indicated by an arrow) since it likely forms a hydrogen bond with H274 and might contribute to the small cavity of AHR-1 ( Figure 6E). We then tested whether mammalian AhR ligands affect the AHR-1 activity when L363 and H365 are mutated. However, these alterations, instead of restoring response to xenobiotic ligands as in zebrafish [101], abolished even the basal AHR-1 activity, similar to the ju145 allele ( Figure 6F). These results show clear differences between the LBDs of C. elegans and zebrafish but display that the LBD is fundamental for basal AHR-1 activity. Together with previous studies [35,38,82], our results suggest that AHR-1 is unlikely to be involved in the classical xenobiotic-induced transactivation response, which thus may not be relevant to ahr-1-regulated physiological aging. Instead, plant-derived compounds might exert conserved effects at least in part via the suppression of AHR-1-modulated pathways. Our 3D model suggests that curcumin does not modulate AHR-1 activity by binding its LBD. Thus, the suppression of AHR-1 activity by curcumin could be due to its antioxidant effect. Consistent with this possibility, and the increased sensitivity of the C. elegans ahr-1 mutants to oxidative stress, we found that AHR-1 activity is indeed increased by ROS-inducing agents. Namely, Cos7 cells treated with the prooxidant rotenone displayed increased AhR activity when transfected with either C. elegans or murine AhR but not when transfected with the ju145 allele or the allele with LBD mutations (Figure 6G,H).
Overall, while CeAhR activation protects against oxidative stress early in life, its decreased expression counteracts aging and mediates the beneficial anti-aging effect of curcumin (Figure 7). Curcumin may thus help balance redox TF activation in a contextand time-dependent manner and favor AhR suppression directly through its antioxidant effect and/or through the activation of Nrf2/SKN-1 (or other TF), which may concurrently mediate the anti-aging activity of curcumin. Antioxidants 2022, 11, x FOR PEER REVIEW 21 of 30   Overall, while CeAhR activation protects against oxidative stress early in life, its decreased expression counteracts aging and mediates the beneficial anti-aging effect of curcumin (Figure 7). Curcumin may thus help balance redox TF activation in a context-and time-dependent manner and favor AhR suppression directly through its antioxidant effect and/or through the activation of Nrf2/SKN-1 (or other TF), which may concurrently mediate the anti-aging activity of curcumin.

Figure 7.
Proposed model of the AHR-1 signaling pathway in C. elegans response to pro-and antioxidants. In "normal" conditions (middle panel), AHR-1 is activated by intra-cellular ROS. This leads to the shedding of the chaperones from cytosolic AHR-1 and the subsequent nuclear translocation of AHR-1. In the nucleus, AHR-1 forms a heterodimer with the AHR nuclear translocator (AHA-1) and bind to XREs of target genes, which in turn leads to the reduction in intracellular ROS levels. In these conditions, loss of ahr-1 function leads to an increased lifespan. In the presence of antioxidants (left panel) the intra-cellular ROS concentrations are low leading to AHR-1 residing in the cytoplasm, bound by its cofactors. The inhibition of the basal AHR-1 activity leads to an increased lifespan. In the presence of pro-oxidants (right panel) AHR-1 is activated by excessive ROS, which results its nuclear translocation, the AHR-1-AHA-1 heterodimer formation and the initiation of target gene transcription. In the ahr-1 KO, the decreased detoxification of ROS through AHR-1induced target genes leads to an accumulation of ROS and renders the ahr-1 KO susceptible. Proposed model of the AHR-1 signaling pathway in C. elegans response to pro-and antioxidants. In "normal" conditions (middle panel), AHR-1 is activated by intra-cellular ROS. This leads to the shedding of the chaperones from cytosolic AHR-1 and the subsequent nuclear translocation of AHR-1. In the nucleus, AHR-1 forms a heterodimer with the AHR nuclear translocator (AHA-1) and bind to XREs of target genes, which in turn leads to the reduction in intracellular ROS levels. In these conditions, loss of ahr-1 function leads to an increased lifespan. In the presence of antioxidants (left panel) the intra-cellular ROS concentrations are low leading to AHR-1 residing in the cytoplasm, bound by its cofactors. The inhibition of the basal AHR-1 activity leads to an increased lifespan. In the presence of pro-oxidants (right panel) AHR-1 is activated by excessive ROS, which results its nuclear translocation, the AHR-1-AHA-1 heterodimer formation and the initiation of target gene transcription. In the ahr-1 KO, the decreased detoxification of ROS through AHR-1-induced target genes leads to an accumulation of ROS and renders the ahr-1 KO susceptible.

Discussion
AhR was originally discovered in mammals for its xenobiotic response activity induced upon binding of environmental toxicants or endogenous ligands, but modulators not relying on ligand binding also exist but are much less investigated. C. elegans represents a unique model organism to investigate AhR activities independent of its classical xenobiotic response since CeAhR does not bind prototype AhR ligands [35,39]. Using this model, we identified an evolutionarily conserved function for AhR in the aging process [14] and showed that some of the mammalian AhR modulators (i.e., bacteria, BaP, and UVB) affect aging parameters through AHR-1 in a context-dependent manner [25]. Here, we followed up on our previous findings with a more mechanistic investigation of AhR-regulated aging features across species by the dietary polyphenol curcumin. Our combined in vivo, in vitro and in silico analyses revealed a new and complex scenario: while curcumin promotes antiaging features in nematodes and human primary EC at least in part in an AhR-dependent manner, its antioxidant effects in both species rely on AhR-independent but primarily Nrf2/SKN-1 dependent mechanisms.
We showed for the first time that curcumin delayed C. elegans' physiological aging in an AHR-1-dependent manner. In search of possible downstream ahr-1-dependent effectors of curcumin, we employed targeted and unbiased approaches and found that the majority of differentially regulated genes upon curcumin treatment are regulated in an AHR-1dependent manner. Moreover, many of these genes displayed a similar expression pattern in AHR-1-depleted and curcumin-treated animals, suggesting that curcumin is promoting lifespan extension via suppression of AHR-1 activity. Surprisingly, neither the targeted nor the transcriptomic analysis indicated a major role for classical AhR targets gens such as cyps, which instead were found largely to be under-expressed in neurons (Larigot et al.; submitted along with this study). Interestingly, these findings may indicate whole animal transcriptomics may mask the neuronal-specific effects of AhR, in this specific case through cyps genes. We found that among the differentially expressed genes, many belong to phase-II-detoxification enzymes, such as ugt-45, which was increased by both ahr-1 depletion (and in the brain of AhR KO mice) and curcumin treatment and to mediate their lifespan extension. Instead, curcumin treatment and ahr-1 depletion increased the expression of another phase-II-detoxification enzyme, gst-4, through different mechanisms: the former relaying on, while the latter mainly independent of, Nrf2/SKN-1, a classical redox TF inducing gst-4 upon oxidative stress in C. elegans [103]. Moreover, while curcumin induces Nrf2/SKN-1-dependent responses in C. elegans (gst-4 expression) and human primary EC (Sod2 expression and migratory capacity), it also protects C. elegans against oxidative stress in a SKN-1-independent manner. In C. elegans, curcumin cannot extend lifespan in the very sick skn-1(zu67) mutants [104], while gst-4 can be induced in a SKN-1-independent manner by EGF signaling [94] and a crosstalk between the EGF pathway and the AhR was reported in mammals [105].
Interestingly, and opposite to the wild-type strain, we observed an AHR-1-independent effect of curcumin on health span in nematode models for Huntington's and Parkinson's disease, respectively. In these strains, curcumin treatment increased the number of protein aggregates to the same extent as AHR-1 deficiency, indicating either a protective effect of the protein aggregation itself and/or curcumin activation of pathways protecting against protein aggregation independently of ahr-1 depletion. The influence of curcumin on protein aggregation is controversial: it was shown to inhibit fibril formation but also to bind pre-fibrillar/oligomeric species of amyloidogenic proteins, thereby accelerating their aggregation and reducing the overall neurotoxicity [106]. Of note, caffeine, which also protects against features of cardiovascular aging [66,107], also prevents Aβ-induced paralysis without decreasing Aβ aggregates but through the activation of the protective Nrf2/SKN-1-dependent pathway [108]. It will be important to assess whether the protective effect induced by curcumin or ahr-1 depletion in the C. elegans disease models is mediated by mechanisms promoting the removal of oligomeric/pre-fibrillar species into less toxic aggregates and/or by the activation of other mechanisms, such as Nrf2/SKN-1, which may concurrently protect against proteotoxicity. Of note, detoxification enzymes may contain both XRE and ARE (antioxidant responsive elements), and an interplay between Nrf2/ARE and AhR/XRE regulated signaling has been described [109]. It will be thus interesting to clarify how curcumin promotes its different beneficial anti-aging effects through the balance between Nrf2 and AhR-regulated signaling.
Our combined approaches showed that curcumin inhibits AHR-1 activity. In mammals, it was suggested the AhR inhibitory effect of curcumin is mediated by direct LBD binding [110] or inhibition of the protein kinase C that phosphorylates AhR [79]. Another study indicated that the transcriptional activity of the AhR is dependent on the cellular redox status and the chromatin structure, which are both influenced by curcumin [111]. While AHR-1 does not bind TCDD, it binds XRE in vitro [36] but systematic studies, addressing the potential of polyaromatic hydrocarbons, or other mammalian AhR ligands to modulate AHR-1, are missing primarily due to the lack of suitable tools to assess that. Our studies attempt to fill this gap and, exploiting Cos7 cells expressing AHR-1 coupled to luciferase assays (Larigot et al.; submitted along with this study) and in silico modeling of C. elegans LBD, revealed that curcumin suppresses AHR-1 activity, but likely not by direct LBD binding. The in vitro assay used in our study confirmed that CeAhR is not activated through the classical xenobiotics signaling. Yet, it would not reveal activities due to AhR binding to DNA sequences other than the "classical" XRE found in CYP1A1 such as the polyphenol(quercetin)-responsive XRE found in PON1 [112,113]. Immunostaining in human primary EC also argues against curcumin inducing AhR nuclear translocation, which, along with the promoting effect of the migratory capacity in AhR overexpressing cells, may also indicate that curcumin suppresses AhR activity.
We propose that the inhibitory effect of curcumin, rather than relying on AhR binding, involves its antioxidant ability, which may indeed be associated with, or even depend on, the activation of Nrf2/SKN-1. Mammalian AhR is activated by ROS via LBD-independent oxidative modification [85], but our data show that the induction of AHR-1 activity by the pro-oxidant rotenone requires the LBD. An indirect mechanism of ROS-mediated AhR activation is the formation of the potent AhR ligand FICZ [114]. Yet, FICZ is a big planar molecule that, according to our in silico model, would not fit the AHR-1 LBD. While the exact mechanism by which AHR-1 activity is promoted by ROS and inhibited by curcumin (either via direct ROS quenching or indirectly via activation of Nrf2 or other antioxidants regulatory genes) remains to be established, this is strongly supported by our findings: AHR-1 is activated by rotenone, and ahr-1 mutants display more mtROS, reduced mitochondrial membrane potential and are more sensitive to H 2 O 2 and juglone as well as to UVB and BaP [25], both of which produce ROS [115,116]. In this context, it is interesting to note that ahr-1 mutants display mild alteration of mitochondrial functions, which resemble those of mitohormesis [117]. This suggests that ahr-1 depletion (and possibly curcumin by inhibiting AHR-1) may promote health span through mild mitochondrial stress, which is known to extend C. elegans lifespan through detoxification genes similarly modulated in the ahr-1 mutants [118,119]. Moreover, whether Nrf2/SKN-1 and mitochondria play a role in modulating AHR-1 activity upon curcumin treatment is an interesting possibility that remains to be validated.
Overall, taking advantage of the multiple features offered by the nematode C. elegans for in vivo studies, we suggest that the ancestral function of the AhR might be in the regulation of phase-II-enzymes related to antioxidant rather than xenobiotic responses. Opposite to the detrimental effects induced by high levels of ROS, the beneficial effects promoted by AhR-deficiency may be mediated by mild mitochondria stress and/or mild ROS production (mitohormesis), which also rely on Nrf2/SKN-1. We also provide strong evidence for the interaction between curcumin and the AhR. Curcumin inhibition of AhR signaling is evolutionarily conserved and is likely not mediated by binding to the AhR LBD, but rather through curcumin's ROS-scavenging properties or the activation of Nrf2/SKN-1. The Nrf2 signaling pathway can indeed be activated by curcumin in different ways [91]. Finally, our data showed that curcumin promotes anti-aging effects also in an AhR-independent manner in both C. elegans (increased gst-4 expression and oxidative stress resistance) and human primary EC (increased Sod2 expression and migratory capacity), which could also explain the additive effects of curcumin and loss of AHR-1 function on the health span of polyQ-expressing animals.

Conclusions
In conclusion, through an original combination of in silico, vitro, and in vivo approaches, we showed that while CeAhR activation protects against oxidative stress early in life, its decreased expression counteracts aging and mediates the beneficial anti-aging effect of curcumin (Figure 7). Curcumin may thus help in balancing the activity of different transcription factors involved in detoxification/antioxidant responses (suppress AhR and activate Nrf2) in conditions where these are altered (increase AhR and decrease Nrf2/SKN-1), such as aging or age-associated disorders. Our work adds a further level of complexity to the already vast multifunctional and context-specific activities of AhR, with important repercussion on organismal health and lifespan. Moreover, it opens the door to additional studies, using the nematode system to discover and investigate ancestral functions of the AhR, which are less likely to be identified in mammals.

Supplementary Materials:
The following supporting information can be downloaded at: https: //www.mdpi.com/article/10.3390/antiox11040613/s1, Figure S1: Cyp-13B1 expression is increased by curcumin in an ahr-1-dependent manner; Figure S2: Tissue-specific gene expression changes in mice; Figure S3: Genes coding for detoxification enzymes are differentially expressed in a tissuespecific manner in mice; Table S1: Primer pairs used for qPCR with C. elegans samples; Table S2: Primer pairs used for qPCR with mouse samples.