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Selenomethionine alleviates AFB1-induced damage in primary chicken hepatocytes by inhibiting CYP450 1A5 expression via upregulated SelW expression Xingxiang Chen, Chaoping Che, Viktor I. Korolchuk, Fang Gan, Cuiling Pan, and Kehe Huang J. Agric. Food Chem., Just Accepted Manuscript • DOI: 10.1021/acs.jafc.6b05308 • Publication Date (Web): 13 Mar 2017 Downloaded from http://pubs.acs.org on March 15, 2017

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Selenomethionine alleviates AFB1-induced damage in primary chicken hepatocytes

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by inhibiting CYP450 1A5 expression via upregulated SelW expression

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Xingxiang Chen †, Chaoping Che †, Viktor I. Korolchuk §, Fang Gan †, Cuiling Pan †,

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Kehe Huang * †

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P. R. China.

College of Veterinary Medicine, Nanjing Agricultural University, Nanjing 210095,

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§

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Tyne, NE4 5PL, UK.

Institute for Cell and Molecular Biosciences, Newcastle University, Newcastle upon

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* Corresponding author.

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Tel.: +86 25 84395507

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Email address: [email protected] (Kehe Huang)

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Abstract

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This study aims to evaluate the protective effects of selenomethionine (SeMet) on

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Aflatoxin B1 (AFB1)-induced hepatotoxicity in primary chicken hepatocytes. Cell

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viability and lactic dehydrogenase activity assays revealed the dose-dependency of

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AFB1 toxicity to chicken hepatocytes. AFB1 concentrations above 0.05 µg/mL

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significantly reduced glutathione and total superoxide dismutase levels, as well as

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increased malondialdehyde concentration and cytochrome P450 enzyme 1A5

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(CYP450 1A5) mRNA levels (P < 0.05). AFB1, however, did not affect CYP450

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3A37 mRNA levels. Supplementation with 2 µM SeMet protected against

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AFB1-induced changes and significantly increased selenoprotein W (SelW) mRNA

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levels (P < 0.05). Additionally, SelW knockdown attenuated the protective effect of

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SeMet on AFB1-induced damage and significantly increased CYP450 1A5 expression

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(P < 0.05). Therefore, SeMet alleviates AFB1-induced damage in primary chicken

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hepatocytes by improving SelW expression, thus inhibiting CYP450 1A5 expression.

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Keywords:

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selenoprotein W, primary chicken hepatocytes

selenomethionine,

AFB1,

cytochrome

P450

37

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enzymes,

siRNA,

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Introduction

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Aflatoxins are produced by different genera of fungi, such as Aspergillus,

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Penicillium, and Fusarium1. The aflatoxin contamination of foods and feeds severely

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affect the health of humans, livestock, and poultry. The Food and Drug Administration

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consider aflatoxins as inevitable contaminants2 with harmful effects, including altered

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production parameters, impaired immunity, or toxicity to multiple organs2-4. In

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addition, aflatoxins are hepatotoxins and hepatocarcinogens5. Structurally, aflatoxins

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are difurocoumarin derivatives that fluoresce under ultraviolet light. Aflatoxins are

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divided based on the color of their fluorescence: aflatoxin B1 and B2 (AFB1, AFB2)

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have blue fluorescence, and G1 and G2 (AFG1, AFG2) have green fluorescence6, 7.

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AFB1 is a potential carcinogen in many species, including humans, birds, swine, fish,

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and rodents8, 9. In poultry, AFB1 decreases serum values of ALT, ALP, total protein,

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and albumin10, 11. AFB1-affected poultry have reduced renal Na⁺ -K⁺ ATPase activity

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and enlarged mitochondria12. AFB1 itself is not toxic but can be bio-activated into the

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highly reactive and toxic intermediate exo-AFB1-8, 9-epoxide (AFBO) by the hepatic

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cytochrome P450 enzyme (CYP450). AFBO reacts with cellular macromolecules,

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such as DNA and proteins, thus causing genotoxicity and cytotoxicity13-15. In nucleic

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acids, AFBO binds to guanine residues, which irreversibly damages DNA in humans,

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primates, and ducks16, 17. CYP450 has two isoforms, 1A5 and 3A37, in the turkey

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liver18-20; these isoforms bioactivate AFB1 into AFBO18, 19, 21 with CYP450 1A5 being

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the dominant enzyme22. AFBO is partly detoxified via conjugation with glutathione

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(GSH). This reaction is catalyzed by glutathione-S-transferases (GST). Moreover,

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AFBO can be detoxified when hydrolyzed either spontaneously or by a cytosolic

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epoxide hydrolase into AFB1-8, 9-dihidrodiol (dhd-AFB1)23. However, further study

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on effective antagonists against AFB1-induced cytotoxicity is still required to reduce

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AFB1-induced damage.

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Selenium (Se) is an essential trace element for animals and humans and has

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diverse biological properties24. Se is involved in the functions of selenoproteins, such

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as glutathione peroxidases (GPx) and selenoprotein W (SelW), which protect cells

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from oxidative stress25-27. Se improves antioxidant activity by enhancing

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selenoprotein levels. Se supplementation in the diet or drinking water inhibits

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carcinogenesis that is induced by numerous chemical carcinogens, including AFB128,

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The covalent binding of AFB1 to liver DNA and RNA is significantly reduced in

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chicks that were fed with a Se-supplemented diet compared with that in control chicks

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that were fed with a basal diet11, 32. The mechanisms involved in the protective effects

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of selenomethionine (SeMet) on AFB1-induced hepatotoxicity, however, remain

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poorly understood.

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. The protective role of Se against aflatoxins has been confirmed in mammals12, 30, 31.

Therefore, this study aims to evaluate and explore the mechanism of the effects

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of SeMet on AFB1-induced hepatotoxicity in primary chicken hepatocytes.

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Materials and Methods

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Isolation and Culture of Chicken Hepatocytes

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All experimental procedures that involved animals were approved by the Animal 4

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Care and Use Committee of Nanjing Agricultural University; the animal ethical

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number is SYXK (Su) 2011-0036. Hepatocytes were obtained from male White

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Leghorn chickens (aged 30–50 days). Hepatocytes were isolated using the previously

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described collagenase perfusion method33. Isolated cells were dispersed in 50 mL of

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serum-free L-15 medium that was supplemented with 0.2% (w/v) bovine serum

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albumin and antibiotics (100 mg/mL streptomycin, 100 IU/mL penicillin, and 0.25

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mg/mL amphotericin B) at 4 °C. Hepatocytes were purified following the method of

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Wu et al (2010)34. The viability of the isolated hepatocytes was 91.5±1.7%, as

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determined via the 0.4 % trypan blue dye exclusion method35 with five different

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preparations of hepatocytes.

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Primary chicken hepatocytes were cultured in accordance with a previous

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method35. Isolated hepatocytes were seeded into 6-well cell culture plates

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(Corning™ Costar™) at a density of 2×106 viable cells per well in 2 mL of L-15

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medium. The L-15 medium was supplemented with 5% fetal bovine serum, 33 mM

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HEPES, 2 mM L-glutamine, 0.2% (w/v) bovine serum albumin, 100 nM

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dexamethasone, 5 mg/L transferrin, 1 mmol/L insulin, and antibiotics, and was

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maintained at pH 7.65. The cells were cultured at 37 °C in a 5% CO2 atmosphere. After

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a plating period of 4 h, the cell monolayers were washed twice with Hanks’ balanced

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salt solution. Then, 3 mL of fresh serum-free L-15 medium was added to each well.

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The spent medium was replaced with fresh serum-free L-15 medium every 24 h.

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Assessment of AFB1 Toxicity

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Isolated chicken hepatocytes were seeded at a density of 2×103/well in 96-well 5

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plates and cultured for 24 h prior to treatment with 0, 0.01, 0.02, 0.05, 0.1, 0.2, 0.4,

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0.8, and 1.6 µg/mL AFB1 (Sigma-Aldrich). AFB1 solutions with different

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concentrations were prepared from a stock solution of 1 mg/mL AFB1 in dimethyl

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sulfoxide (DMSO). The stock solution was further diluted in culture media at the

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desired concentrations. The cells were then cultured at 37 °C in a 5% CO2 atmosphere

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for 24 h to reach 80% confluence and were then subjected to the colorimetric

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3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay (Sigma, USA).

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Absorbance was measured at 490 nm with a reference wavelength of 630 nm. Lactic

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dehydrogenase (LDH) activity in the incubation medium was measured as previously

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described35. One unit of enzyme activity was defined as 1 mmol of reduced

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nicotinamide adenine dinucleotide oxidized per min. LDH activity in the culture

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medium was expressed as units per liter. All samples were assayed in triplicate.

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Measurements of GSH, SOD, and MDA

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Cells were removed from wells. Cell extracts were then prepared by sonicating

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cells in ice-cold phosphate-buffered saline. After sonication, cell lysates were

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centrifuged at 10,000×g for 20 min to remove cell debris. Reduced GSH, superoxide

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dismutase activity (SOD), and maliondehyde (MDA) were measured in the

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supernatants as previously described using commercially available kits (Jiancheng Co.,

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China)36, 37. GSH was spectrophotometrically measured (412nm) through reaction

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with 5, 5′-dithiobis (2-nitrobenzoic acid). GSH concentrations were expressed as

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micromoles of GSH per gram of protein. SOD activity was assayed via oxyamine

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oxidation inhibition by xanthine oxidase. One unit of SOD activity was defined as the 6

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quantity that reduced absorbance at 550 nm by 50%. Results were expressed as unit

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per milligram protein. MDA concentration was spectrophotometrically assayed at 548

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nm via the thiobarbituric acid reaction and was expressed as micromoles per gram of

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protein. Total protein concentration was determined using a Bradford Protein Assay

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Kit (Beyotime, China). All samples were assayed in triplicate.

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siRNA Transfection

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Double-stranded RNA sequences were designed based on the sequence of Gallus

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gallus SelW mRNA (GenBank Accession No. GQ919055) using Invitrogen BlockiT

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RNAi designer. RNA sequences were synthesized by Invitrogen. The SelW-specific

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siRNA sequence was 5’-CGGCUUCGUGGACACCGACGCCAAA-3’. The control

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siRNA sequence was 5’-CGGUCGUGGACACCGACGCCCUAAA-3’. Duplexes

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were resuspended in DEPC-treated water to obtain 20 mM solutions prior to use.

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Chicken hepatocytes in DMEM with 10% FBS without antibiotics were seeded in

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24-well plates at 5×104 cells/well and incubated for 24 h at 37 °C in a 5% CO2

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atmosphere. When the cells reached 30%–50% confluence, siRNA was introduced

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using the X-tremeGene siRNA transfection reagent (Roche, USA) in accordance with

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the manufacturer’s protocol.

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Real-time PCR

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SelW, CYP450 1A5, and 3A37 mRNA levels were quantitatively determined by

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real-time PCR. Total RNA was extracted from cells using Trizol (Invitrogen, USA) in

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accordance with the manufacturer’s protocol. DNA contamination was prevented with

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the DNA-Free kit (TaKaRa, China). RNA quality was assessed via agarose gel (1%)

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electrophoresis and spectrophotometry

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reverse-transcribed to complimentary DNA (cDNA) using the PrimeScriptTM RT

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Master Mix kit (TaKaRa, China). The resulting first-strand cDNA was stored at

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−20 °C until used for real-time PCR. Specific primers for β-actin, SelW, CYP450 1A5,

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and 3A37 were designed with Primer Premier Software (Premier Biosoft International,

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USA) based on known sequences (Table 1). qRT-PCR was performed with an

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ABI-Prism7300 detection system (Applied Biosystems, USA). Reactions were

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performed in a 25-µL reaction mixture that contained 12.5 µL of 2×SYBR Green I

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PCR Master Mix (TaKaRa, China), 10 µL of cDNA, 1 µL of each primer (10 µM),

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and 0.5 µL of PCR-grade water. The qRT-PCR program consisted of a 95 °C step for

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30 s, followed by 40 cycles of 95 °C for 5 s, and 60 °C for 31 s. A dissociation curve

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was obtained per plate to confirm the production of a single product. Considering that

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different treatments had no effects on β-actin Ct values in our study (data not shown),

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the mRNA levels of SelW, CYP450 1A5, and 3A37 relative to that of the reference

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β-actin gene were determined using the ∆ cycle threshold (∆Ct) method as outlined in

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the protocol provided by Applied Biosystems. The result was applied to each gene by

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calculating the expression 2−∆∆CT.

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Western Blot

(A260/A280). Total

RNA (1 µg) was

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The relative abundance of CYP450 1A5 protein in hepatocytes after siRNA

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interference was determined by Western blot. Cell samples were lysed via ultrasound

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at 4 °C in radioimmunoprecipitation assay buffer with protease inhibitors. The lysates 8

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were centrifuged at 12,000×g for 15 min at 4 °C. Total protein concentrations were

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determined using the bicinchoninic acid protein assay. Then, 40 µg of proteins in

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loading buffer were denatured by heating at 95 °C for 5 min, separated by SDS-PAGE

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on 4–12% Bis-Tris gel, and transferred onto a polyvinylidene fluoride membrane.

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After blocking, the membranes were individually incubated overnight at 4 °C with

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primary antibodies against CYP450 1A5 (rabbit anti-human CYP450, BIOSS) at a

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concentration of 1:500 and with primary antibodies against β-actin (Cell Signaling

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Technology, USA) at a concentration of 1:1,000. Membranes were then washed and

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incubated at room temperature for 30 min with horseradish peroxidase-conjugated

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secondary antibody (1:5,000 donkey anti-rabbit IgG Santa Cruz, Biotech, USA) for

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chemiluminescence detection. Proteins were visualized using a Bio-Imaging analyzer

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(LAS-3000, Japan). Band intensity was quantified with ImageQuant TL software (GE

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Healthcare, UK).

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Statistical Analysis

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Data were analyzed with SPSS 18.0 software (SPSS, USA). Experimental results

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were expressed as mean ± SEM. Statistical significance was tested with one-way

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ANOVA, followed by Duncan’s multiple range test. P-values < 0.05 were considered

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statistically significant.

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Results

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Cytotoxicity of Various AFB1 Concentrations to Chicken Hepatocytes

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As shown in Fig. 1, treatment with DMSO, which was used as the AFB1 solvent, 9

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did not significantly change cell viability and LDH activities compared with the

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control treatment (P > 0.05). The toxic effects of 0–1.6 µg/mL AFB1 on the cell

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viability (Fig. 1A) and LDH activities (Fig. 1B) of chicken hepatocytes were

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concentration-dependent. Treatment with 0.05, 0.1, 0.2, 0.4, 0.8, and 1.6 µg/mL AFB1

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significantly decreased cell viability compared with DMSO treatment (P < 0.05). The

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changes in LDH activities caused by AFB1 treatment were opposite to the changes in

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cell viability. Treatment with 0.05, 0.1, 0.2, 0.4, 0.8, and 1.6 µg/mL AFB1

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significantly increased LDH activities compared with DMSO treatment (P < 0.05).

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LDH activities plateaued with 0.2–1.6 µg/mL AFB1 treatment. Our data revealed that

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0.05 µg/mL or higher concentrations of AFB1 had significant cytotoxic effects on cell

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viability and LDH activities in chicken hepatocytes. Therefore, 0.05 µg/mL AFB1 was

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used in the subsequent experiments.

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Protective Effects of SeMet Against AFB1-induced Toxicity in Chicken Hepatocytes

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Various concentrations of SeMet (0, 0.5, 1, 2, and 4 µM) were used to evaluate

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the protective effect of SeMet against AFB1 toxicity. Compared with the control

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group, the cell viability in the groups without AFB1 treatment was significant and was

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promoted by 12% and 13% when SeMet was supplemented at concentrations of 1 and

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2 µM, respectively. The group that was treated with 0.05 µg/mL AFB1 had

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significantly reduced cell viability compared with the control group; however, these

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reductions were lower when 0.5, 1, 2, and 4 µM SeMet concentrations were

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supplemented (Fig. 2A). As shown in Fig. 2B, supplementation with 0.05 µg/mL

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AFB1 increased LDH activity by 35% compared with the control treatment. However, 10

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LDH activities increased by only 32%, 27%, 25%, and 13% when SeMet was

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supplemented at concentrations of 0.5, 1, 2, and 4 µM, respectively, compared with

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the control treatment (P < 0.05). Our data revealed that SeMet has protective effects

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against AFB1-induced toxicity in chicken hepatocytes.

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Effect of SeMet on GSH, MDA, and SOD Levels in AFB1-treated Chicken

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Hepatocytes

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As shown in Fig. 3A, SeMet treatment significantly enhanced intracellular GSH

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concentrations compared with the control treatment (P < 0.05). The maximum GSH

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level was obtained with 2 µM SeMet. Hepatocytes that were treated with 0.05 µg/mL

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AFB1 alone showed lower GSH levels than the control group that did not receive

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AFB1 and SeMet treatment (P < 0.05). Pretreatment with various SeMet

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concentrations significantly increased GSH levels in AFB1-treated chicken

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hepatocytes recovered compared with the control group that did not receive SeMet

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treatment (P < 0.05). After treatment with 0.05 µg/mL AFB1, the highest GSH level

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was observed in hepatocytes that were pretreated with 2 µM SeMet; this level as close

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to the normal level in the control group that did not receive AFB1 and SeMet

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treatment.

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MDA levels in chicken hepatocytes are presented in Fig. 3B. As shown in the

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figure, MDA levels declined when hepatocytes were treated with various

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concentrations of SeMet alone; however, only the MDA level of the group that was

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treated with 2 µM SeMet significantly decreased compared with that of the control

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group (P < 0.05). The MDA level in the hepatocytes that were treated with 0.05 11

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µg/mL AFB1 alone significantly increased compared with that in the untreated

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hepatocytes (P < 0.05). Pretreatment with 1 µM SeMet reduced MDA levels that were

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increased in AFB1-treated chicken hepatocytes. Pretreatment with 2 µM SeMet

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caused the highest reduction of MDA levels in AFB1-treated chicken hepatocytes.

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SOD levels in chicken hepatocytes are presented in Fig. 3C. SOD levels in

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chicken hepatocytes that were treated with 1 µM SeMet significantly increased

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compared with that in control cells that were not treated with SeMet (P < 0.05).

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Treatment with 2 µM SeMet maximized SOD levels. Treatment with AFB1 alone

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significantly reduced SOD levels in chicken hepatocytes compared with in chicken

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hepatocytes that did not receive AFB1 treatment (P < 0.05). Furthermore, SOD levels

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significantly increased in AFB1-treated chicken hepatocytes that were pretreated with

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1 µM SeMet compared with those that were treated with AFB1 alone (P < 0.05).

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SeMet Increases the mRNA Level of SelW in Primary Chicken Hepatocytes with or

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without AFB1 Treatment

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The effects of SeMet (0, 0.5, 1, 2, and 4 µM) on SelW mRNA levels were

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determined to further investigate the mechanism responsible for the protective role of

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SeMet in AFB1-damaged primary chicken hepatocytes. As shown in Fig. 4,

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quantitative RT-PCR analysis revealed that compared with the control treatment,

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supplementation with 0.5, 1, 2, and 4 µM SeMet significantly increased SelW mRNA

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levels in primary chicken hepatocytes without AFB1 treatment (P < 0.05). Compared

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with the control treatment, supplementation with 1, 2, and 4 µM SeMet significantly

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increased SelW mRNA levels in AFB1-treated primary chicken hepatocytes (P < 12

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0.05). These data suggested that SeMet supplementation decreases AFB1-induced

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damages in primary chicken hepatocytes by improving SelW expression.

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SeMet Reduces the mRNA Levels of CYP450 1A5 but not of 3A37 in Primary Chicken

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Hepatocytes with or without AFB1 treatment

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The relative mRNA levels of CYP450 1A5 and 3A37 in each group were

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quantified and are shown in Fig. 5. CYP450 1A5 mRNA levels in hepatocytes that

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were treated with 1 and 2 µM SeMet alone were significantly lower than those in

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hepatocytes that were treated with 0 µM SeMet (P < 0.05). Compared with the control

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treatment, treatment with 0.05 µg/mL AFB1 significantly increased CYP450 1A5

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mRNA levels in hepatocytes (P < 0.05). Treatment with various SeMet concentrations

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(P < 0.05) reduced CYP450 1A5 mRNA levels that were increased by treatment with

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0.05 µg/mL AFB1. In addition, the lowest CYP450 1A5 mRNA levels were observed

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in the hepatocytes that were treated with 2 µM SeMet in the presence or absence of

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AFB1. However, SeMet and AFB1 treatment did not significantly influence CYP450

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3A37 mRNA levels in hepatocytes (P > 0.05) (Fig. 5B).

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Effect of SelW Knockdown on SelW mRNA Levels, Cell Viability, and LDH Activity in

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Primary Chicken Hepatocytes

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SelW mRNA levels were determined after hepatocytes were transfected with

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either SelW-specific or control siRNA (Fig. 6A). As shown in Fig. 6A, treatment with

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SelW-specific siRNA significantly decreased SelW mRNA levels in chicken

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hepatocytes compared with the control treatment at 24, 48, and 72 h after transfection

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(P < 0.05). SeMet supplementation significantly increased SelW mRNA levels in

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untransfected hepatocytes and control-siRNA transfected hepatocytes compared with

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the control group (P < 0.05). However, SeMet supplementation did not influence

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SelW mRNA levels in hepatocytes that were transfected with SelW-specific siRNA at

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48 h after transfection.

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As shown in Fig. 6B, compared with the control treatment, AFB1 treatment

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significantly reduced the cell viabilities of groups without siRNA treatment or with

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control-siRNA treatment (P < 0.05). By contrast, SeMet treatment protected primary

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chicken hepatocytes against AFB1-induced damage by maintaining cell viability at

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levels similar to those of the controls. SeMet treatment significantly increased

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AFB1-reduced cell viabilities in the groups with SelW-specific siRNA treatment (P
0.05).

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SelW Knockdown Influences the Effects of SeMet on CYP450 1A5 in Primary Chicken

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Hepatocytes with or without AFB1 treatment 14

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To investigate the mechanism that changed CYP450 1A5 mRNA levels in

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response to SeMet supplementation in AFB1-induced hepatocytes, the effects of

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SeMet supplementation on CYP450 1A5 was evaluated in SelW-knockdown

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hepatocytes. As shown in Figs. 7A and 7B, compared with relative controls,

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supplementation with 2 µM SeMet significantly inhibited the increase in the mRNA

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and protein levels of CYP450 1A5 in untransfected or control-siRNA transfected

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hepatocytes (P < 0.05) but not in the hepatocytes that were transfected with

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SelW-specific siRNA (P > 0.05).

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Discussion

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The potential protective effects of SeMet on AFB1-induced damages in primary

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chicken hepatocytes were evaluated in the present study. Results showed that AFB1

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significantly reduced cell viability, GSH, and SOD levels but increased MDA level

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and LDH activity. These results indicated that AFB1 causes oxidative stress in

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chicken hepatocytes. These results are in agreement with those of a previous in vitro

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study, which reported that AFB1 treatment significantly increased oxidative stress in

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MDCK cells, as evidenced by the decreased cell viability, GSH level and activity, and

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GPX1 mRNA levels and increased MDA levels of AFB1-treated MDCK cells38.

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Moreover, SeMet treatment significantly alleviated AFB1-induced oxidative stress in

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primary chicken hepatocytes.

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AFB1 is bioactivated to a toxic intermediate that causes genotoxicity by reacting

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with DNA and that causes cytotoxicity by interacting with proteins13, 14. Previous

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studies established that two important CYP450 isoforms, CYP450 1A5 and 3A37,

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which are orthologs of human P450 1A2 and 3A4, respectively, bioactivate AFB1 in

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the turkey liver18, 19, 21. Furthermore, CYP450 1A5 is the dominant enzyme in the

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bioactivation and metabolism of AFB1 in turkey liver that was treated with AFB1 at

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environmentally relevant concentrations22. The present findings for primary chicken

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hepatocytes were partially consistent with those of a previous study on turkeys. Our

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results revealed that treatment with 0.05 µg/mL AFB1 significantly increases CYP450

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1A5 mRNA levels but does not influence CYP450 3A37 mRNA levels. Our results

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implicated CYP450 1A5, instead of CYP450 3A37, in AFB1 metabolism in primary

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chicken hepatocytes that were exposed to 0.05 µg/mL AFB1.

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Se is an essential micronutrient for animals and humans and has an important

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role in antioxidant defense systems25. Se supplementation against aflatoxins is a

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common practice and has been applied in animal feeds for many years30. Se improves

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antioxidant activities by enhancing GSH levels39, as observed in the present study.

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SeMet, an organic form of Se, is more bioavailable than the inorganic forms of Se,

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such as Na2SeO3. SeMet pretreatment increased cell viability and GSH and SOD

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levels, as well as reduced MDA levels and LDH activities, in AFB1-treated primary

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chicken hepatocytes. These findings suggested that SeMet alleviates AFB1-induced

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oxidative stress in primary chicken hepatocytes. CYP450 1A5 mRNA levels in

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chicken hepatocytes that were treated with AFB1 and SeMet were significantly lower

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than those in chicken hepatocytes that were treated with AFB1 only. This finding

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indicated that SeMet protects chicken hepatocytes against AFB1-induced damages by

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suppressing the expression of CYP450 1A5 mRNA and then reducing the levels of

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AFB1, which is bioactivated into the toxic exo-AFBO by CYP450 1A5.

345

Se, an essential micronutrient with major metabolic significance, is incorporated

346

as selenocysteine at the active sites of numerous proteins40. SelW, the smallest

347

identified selenoprotein, regulates cellular redox41, 42, cell cycle progression, and cell

348

proliferation43-46. SelW is essential for the maintenance of normal liver function, and

349

the expression of SelW in the liver depends on the level of dietary Se47, 48. In this

350

study, SeMet treatment suppressed the mRNA levels of CYP450 1A5, a

351

phaseⅠdrug-metabolizing enzyme that activates AFB1 to toxic AFBO in the liver18, 19,

352

21, 49

353

primary chicken hepatocytes with or without AFB1 treatment (P < 0.05). Chicken

354

hepatocytes were cultured overnight and then transfected with SelW-specific or

355

control siRNA to investigate the suppressive effect of SelW on AFB1-induced

356

CYP450 1A5 expression in chicken hepatocytes. As shown in Fig. 7 (A and B),

357

SeMet treatment significantly decreased CYP450 1A5 expression in primary chicken

358

hepatocytes that were transfected with control siRNA, but did not decrease CYP450

359

1A5 expression in primary chicken hepatocytes that were transfected with

360

SelW-specific siRNA. These findings revealed that SeMet protects primary chicken

361

hepatocytes from AFB1-induced damage by inhibiting CYP450 1A5 expression to

362

reduce AFBO production and then reduce the combination between liver DNA and

363

RNA. Our data offer more insights than a previous in vivo study that focused on the

364

prevention of aflatoxin b1 hepatoxicity by dietary Se, which is associated with the

. In addition, SeMet treatment significantly increased the mRNA level of SelW in

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inhibition of cytochrome p450 isozymes in chicken liver 11.

366

Some studies have reported that the increase in GSH levels via selenoproteins is

367

responsible for the protective effects of Se against AFB1 toxicity38, 50. Some studies

368

have also shown that Se directly regulates Cytochrome P450, the key enzyme in the

369

bio-activation of AFB1. Se-enriched polysaccharides exert anti-mutagenic effects in

370

the mouse liver by suppressing the Cytochrome P450 1A subfamily51. The potential

371

and selective inhibition of CYP1A1 by SeCys conjugates contributes to their

372

chemopreventive activity52. Four chemopreventive organoselenium compounds have

373

spectral modification and catalytic inhibition activities on human cytochrome P45053.

374

The protective effect of dietary Se on AFB1-induced hepatoxicity in chickens is

375

associated with the inhibition of cytochrome p450 isozymes11. We found that SeMet

376

enhanced the anti-oxidative status of AFB1-treated primary chicken hepatocytes by

377

increasing GSH levels and SOD concentration and by reducing MDA (Fig. 3).

378

Moreover, we found that SeMet inhibited CYP450 1A5 expression by improving

379

SelW expression. Given that cytochrome P450 is the key enzyme for the bioactivation

380

of AFB1 into the reactive epoxide intermediate AFBO54, 55, we concluded that SeMet

381

alleviates AFB1-induced damages in primary chicken hepatocytes by improving SelW

382

expression, thus inhibiting CYP450 1A5 expression.

383

In summary, supplementation with 2 µM SeMet protects primary chicken

384

hepatocytes from AFB1-induced damage. SeMet supplementation maintains cell

385

viability, GSH activity, SOD levels, LDH levels, and MDA levels by increasing SelW

386

mRNA levels and decreasing CYP450 1A5 mRNA levels. Knockdown of SelW with

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SelW-specific siRNA significantly increases the mRNA and protein levels of CYP450

388

1A5 (P < 0.05), thus indicating that SeMet alleviates AFB1-induced damage in

389

primary chicken hepatocytes by improving SelW expression and inhibiting CYP450

390

1A5 expression. Further research is still required on the protective mechanism of

391

SelW against AFB1-induced cellular damage.

392

Acknowledgment

393

This work was funded by the National Natural Science Foundation of China (NFSC)

394

(31472253, 31472252), the Fundamental Research Funds for the Central Universities

395

(Y0201500198) and the Priority Academic Program Development of Jiangsu Higher

396

Education Institutions (Jiangsu, China).

397

References

398 399 400 401 402 403 404 405 406 407 408 409 410 411 412 413 414 415

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mechanistic and translational toxicology. Toxicol Sci 2011, 120 Suppl 1, S28-48. (10) Hussain, Z.; Rehman, H. U.; Manzoor, S.; Tahir, S.; Mukhtar, M. Determination of liver and muscle aflatoxin B1 residues and select serum chemistry variables during chronic aflatoxicosis in broiler chickens. Vet Clin Pathol 2016, 45 (2), 330-4. (11) Sun, L. H.; Zhang, N. Y.; Zhu, M. K.; Zhao, L.; Zhou, J. C.; Qi, D. S. Prevention of Aflatoxin B1 Hepatoxicity by Dietary Selenium Is Associated with Inhibition of Cytochrome P450 Isozymes and Up-Regulation of 6 Selenoprotein Genes in Chick Liver. J Nutr 2016. (12) Liang, N.; Wang, F.; Peng, X.; Fang, J.; Cui, H.; Chen, Z.; Lai, W.; Zhou, Y.; Geng, Y. Effect of Sodium Selenite on Pathological Changes and Renal Functions in Broilers Fed a Diet Containing Aflatoxin B(1). Int J Environ Res Public Health 2015, 12 (9), 11196-208. (13) Doi, A. M.; Patterson, P. E.; Gallagher, E. P. Variability in aflatoxin B(1)-macromolecular binding and relationship to biotransformation enzyme expression in human prenatal and adult liver. Toxicol Appl Pharmacol 2002, 181 (1), 48-59. (14) Cervino, C.; Knopp, D.; Weller, M. G.; Niessner, R. Novel Aflatoxin Derivatives and Protein Conjugates. Molecules 2007, 12 (3), 641-653. (15) Shi, D.; Liao, S.; Guo, S.; Li, H.; Yang, M.; Tang, Z. Protective effects of selenium on aflatoxin B1-induced mitochondrial permeability transition, DNA damage, and histological alterations in duckling liver. Biol Trace Elem Res 2015, 163 (1-2), 162-8. (16) Verma, R. J. Aflatoxin causes DNA damage. Int. J. Hum. Genet. 2004, 4 (4), 231-236. (17) Do, J.; Choi, D.-K. Aflatoxins: Detection, toxicity, and biosynthesis. Biotechnol. Bioprocess Eng. 2007, 12 (6), 585-593. (18) Yip, S. S.; Coulombe, R. A., Jr. Molecular cloning and expression of a novel cytochrome p450 from turkey liver with aflatoxin b1 oxidizing activity. Chem Res Toxicol 2006, 19 (1), 30-7. (19) Rawal, S.; Yip, S. S.; Coulombe, R. A., Jr. Cloning, expression and functional characterization of cytochrome P450 3A37 from turkey liver with high aflatoxin B1 epoxidation activity. Chem Res Toxicol 2010, 23 (8), 1322-9. (20) Rawal, S.; Mendoza, K. M.; Reed, K. M.; Coulombe, R. A., Jr. Structure, genetic mapping, and function of the cytochrome P450 3A37 gene in the turkey (Meleagris gallopavo). Cytogenet Genome Res 2009, 125 (1), 67-73. (21) Klein, P. J.; Buckner, R.; Kelly, J.; Coulombe, R. A., Jr. Biochemical basis for the extreme sensitivity of turkeys to aflatoxin B(1). Toxicol Appl Pharmacol 2000, 165 (1), 45-52. (22) Rawal, S.; Coulombe, R. A., Jr. Metabolism of aflatoxin B1 in turkey liver microsomes: the relative roles of cytochromes P450 1A5 and 3A37. Toxicol Appl Pharmacol 2011, 254 (3), 349-54. (23) Eaton, D. L.; Gallagher, E. P. Mechanisms of aflatoxin carcinogenesis. Ann. Rev. Pharmacol. Toxicol. 1994, 34, 135-172. (24) Arthur, J. R.; Beckett, G. J. New metabolic roles for selenium. Proc. Nutr. Soc. 1994, 53 (3), 615-624. (25) Soudani, N.; Ben Amara, I.; Sefi, M.; Boudawara, T.; Zeghal, N. Effects of selenium on chromium (VI)-induced hepatotoxicity in adult rats. Exp Toxicol Pathol 2011, 63 (6), 541-8. (26) Jeong, D.; Kim, T. S.; Chung, Y. W.; Lee, B. J.; Kim, I. Y. Selenoprotein W is a glutathione-dependent antioxidant in vivo. FEBS Lett 2002, 517 (1-3), 225-8. (27) Xiao-Long, W.; Chuan-Ping, Y.; Kai, X.; Ou-Jv, Q. Selenoprotein W depletion in vitro might indicate that its main function is not as an antioxidative enzyme. Biochemistry (Mosc) 2010, 75 (2), 201-7.

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(28) Griffin, A. C. Role of selenium in the chemoprevention of cancer. Adv Cancer Res 1979, 29, 419-42. (29) Chen, J.; Goetchius, M. P.; Campbell, T. C.; Combs, G. F., Jr. Effects of dietary selenium and vitamin E on hepatic mixed-function oxidase activities and in vivo covalent binding of aflatoxin B1 in rats. J Nutr 1982, 112 (2), 324-31. (30) Davila, J. C.; Edds, G. T.; Osuna, O.; Simpson, C. F. Modification of the effects of aflatoxin B1 and warfarin in young pigs given selenium. Am J Vet Res 1983, 44 (10), 1877-83. (31) Yu, Z.; Wang, F.; Liang, N.; Wang, C.; Peng, X.; Fang, J.; Cui, H.; Jameel Mughal, M.; Lai, W. Effect of Selenium Supplementation on Apoptosis and Cell Cycle Blockage of Renal Cells in Broilers Fed a Diet Containing Aflatoxin B1. Biol Trace Elem Res 2015, 168 (1), 242-51. (32) Chen, J.; Goetchius, M. P.; Combs, G. F.; Campbell, T. C. Effects of dietary selenium and vitamin E on covalent binding of aflatoxin to chick

liver cell macromolecules. J. Nutr 1982, 112, 350-357.

(33) Fujii, M.; Yoshino, I.; Suzuki, M.; Higuchi, T.; Mukai, S.; Aoki, T.; Fukunaga, T.; Sugimoto, Y.; Inoue, Y.; Kusuda, J.; Saheki, T.; Sato, M.; Hayashi, S.; Tamaki, M.; Sugano, T. Primary culture of chicken hepatocytes in serum-free medium (pH 7.8) secreted albumin and transferrin for a long period in free gas exchange with atmosphere. Int. J. Biochem. Cell Biol. 1996, 28 (12), 1381-1391. (34) Wu, X.; Huang, K.; Wei, C.; Chen, F.; Pan, C. Regulation of cellular glutathione peroxidase by different forms and concentrations of selenium in primary cultured bovine hepatocytes. J Nutr Biochem 2010, 21 (2), 153-61. (35) Wu, X.; Wei, C.; Pan, C.; Duan, Y.; Huang, K. Regulation of expression and activity of selenoenzymes by different forms and concentrations of selenium in primary cultured chicken hepatocytes. Br J Nutr 2010, 104 (11), 1605-12. (36) Rahman, I.; Kode, A.; Biswas, S. K. Assay for quantitative determination of glutathione and glutathione disulfide levels using enzymatic recycling method. Nat Protoc 2006, 1 (6), 3159-65. (37) Gavino, V. C.; Miller, J. S.; Ikharebha, S. O.; Milo, G. E.; Cornwell, D. G. Effect of polyunsaturated fatty acids and antioxidants on lipid peroxidation in tissue cultures. J Lipid Res 1981, 22 (5), 763-9. (38) Parveen, F.; Nizamani, Z. A.; Gan, F.; Chen, X.; Shi, X.; Kumbhar, S.; Zeb, A.; Huang, K. Protective effect of selenomethionine on aflatoxin B1-induced oxidative stress in MDCK cells. Biol Trace Elem Res 2014, 157 (3), 266-74. (39) Kim, S. S.; Koo, J. H.; Kwon, I. S.; Oh, Y. S.; Lee, S. J.; Kim, E. J.; Kim, W. K.; Lee, J.; Cho, J. Y. Exercise training and selenium or a combined treatment ameliorates aberrant expression of glucose and lactate metabolic proteins in skeletal muscle in a rodent model of diabetes. Nutr Res Pract 2011, 5 (3), 205-13. (40) Papp, L. V.; Holmgren, A.; Khanna, K. K. Selenium and selenoproteins in health and disease. Antioxid Redox Signal 2010, 12 (7), 793-5. (41) Dikiy, A.; Novoselov, S. V.; Fomenko, D. E.; Sengupta, A.; Carlson, B. A.; Cerny, R. L.; Ginalski, K.; Grishin, N. V.; Hatfield, D. L.; Gladyshev, V. N. SelT, SelW, SelH, and Rdx12: genomics and molecular insights into the functions of selenoproteins of a novel thioredoxin-like family. Biochemistry 2007, 46 (23), 6871-82. (42) Jeon, Y. H.; Ko, K. Y.; Lee, J. H.; Park, K. J.; Jang, J. K.; Kim, I. Y. Identification of a redox-modulatory interaction between selenoprotein W and 14-3-3 protein. Biochim Biophys Acta 2016, 1863 (1), 10-8. (43) Hawkes, W. C.; Printsev, I.; Alkan, Z. Selenoprotein W depletion induces a p53- and

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p21-dependent delay in cell cycle progression in RWPE-1 prostate epithelial cells. J Cell Biochem 2012, 113 (1), 61-9. (44) Hawkes, W. C.; Alkan, Z. Delayed cell cycle progression in selenoprotein W-depleted cells is regulated by a mitogen-activated protein kinase kinase 4-p38/c-Jun NH2-terminal kinase-p53 pathway. J Biol Chem 2012, 287 (33), 27371-9. (45) Noh, O. J.; Park, Y. H.; Chung, Y. W.; Kim, I. Y. Transcriptional regulation of selenoprotein W by MyoD during early skeletal muscle differentiation. J Biol Chem 2010, 285 (52), 40496-507. (46) Hawkes, W. C.; Wang, T. T.; Alkan, Z.; Richter, B. D.; Dawson, K. Selenoprotein W modulates control of cell cycle entry. Biol Trace Elem Res 2009, 131 (3), 229-44. (47) Sun, B.; Wang, R.; Li, J.; Jiang, Z.; Xu, S. Dietary selenium affects selenoprotein W gene expression in the liver of chicken. Biol Trace Elem Res 2011, 143 (3), 1516-23. (48) Li, J. L.; Ruan, H. F.; Li, H. X.; Li, S.; Xu, S. W.; Tang, Z. X. Molecular cloning, characterization and mRNA expression analysis of a novel selenoprotein: avian selenoprotein W from chicken. Mol Biol Rep 2011, 38 (6), 4015-22. (49) Monroe, D. H.; Eaton, D. L. Comparative effects of butylated hydroxyanisole on hepatic in vivo DNA binding and in vitro biotransformation of aflatoxin B1 in the rat and mouse. Toxicol Appl Pharmacol 1987, 90 (3), 401-9. (50) Shi, D.; Guo, S.; Liao, S.; Su, R.; Pan, J.; Lin, Y.; Tang, Z. Influence of selenium on hepatic mitochondrial antioxidant capacity in ducklings intoxicated with aflatoxin B(1). Biol Trace Elem Res 2012, 145 (3), 325-9. (51) Peng, F.; Guo, X.; Li, Z.; Li, C.; Wang, C.; Lv, W.; Wang, J.; Xiao, F.; Kamal, M. A.; Yuan, C. Antimutagenic Effects of Selenium-Enriched Polysaccharides from Pyracantha fortuneana through Suppression of Cytochrome P450 1A Subfamily in the Mouse Liver. Molecules 2016, 21 (12). (52) Venhorst, J.; Rooseboom, M.; Vermeulen, N. P.; Commandeur, J. N. Studies on the inhibition of human cytochromes P450 by selenocysteine Se-conjugates. Xenobiotica 2003, 33 (1), 57-72. (53) Shimada, T.; Murayama, N.; Tanaka, K.; Takenaka, S.; Guengerich, F. P.; Yamazaki, H.; Komori, M. Spectral modification and catalytic inhibition of human cytochromes P450 1A1, 1A2, 1B1, 2A6, and 2A13 by four chemopreventive organoselenium compounds. Chem Res Toxicol 2011, 24 (8), 1327-37. (54) Diaz, G. J.; Murcia, H. W.; Cepeda, S. M. Cytochrome P450 enzymes involved in the metabolism of aflatoxin B1 in chickens and quail. Poult Sci 2010, 89 (11), 2461-9. (55) Gallagher, E. P.; Kunze, K. L.; Stapleton, P. L.; Eaton, D. L. The kinetics of aflatoxin B1 oxidation by human cDNA-expressed and human liver microsomal cytochromes P450 1A2 and 3A4. Toxicol Appl Pharmacol 1996, 141 (2), 595-606.

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Figure captions

544

Fig. 1 Effects of Various Concentration of AFB1 on Cell Viability (A) and LDH

545

Activity (B) in Chicken Hepatocytes.

546

Values are represented as means ± SEM from three experiments (n=3). Groups

547

were compared by one-way ANOVA followed by Duncan’s multiple range tests.

548

Asterisk means values were significantly different from the control (P < 0.05).

549 550

Fig. 2 Protective Effect of SeMet on Cell Viability (A) and LDH Activity (B) in

551

AFB1-treated Chicken Hepatocytes

552

Values are represented as means ± SEM from three experiments (n=3). Groups

553

were compared by a 1-way ANOVA followed by Duncan’s multiple range tests. Within the

554

groups without AFB1 treatment, bars with * are significantly different from the control cells

555

(P < 0.05). Within the groups with 0.05µg/ml AFB1 treatment, bars with # are significantly

556

different from the control cells (P < 0.05). Significant changes are indicated by & in

557

comparison between treated cells and untreated cells by 0.05µg/ml AFB (P < 0.05).

558

559

Fig. 3 Effect of SeMet on GSH (A), MDA (B) and SOD (C) Levels in AFB1-treated

560

Chicken Hepatocytes

561

Values are represented as means ± SEM from three experiments (n=3). Groups

562

were compared by a 1-way ANOVA followed by Duncan’s multiple range tests. Within the

563

groups without AFB1 treatment, bars with * are significantly different from the control cells

564

(P < 0.05). Within the groups with 0.05µg/ml AFB1 treatment, bars with # are significantly 23

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565

different from the control cells (P < 0.05). Significant changes are indicated by & in

566

comparison between treated cells and untreated cells by 0.05µg/ml AFB (P < 0.05).

567 568

Fig. 4 Effect of SeMet on SelW mRNA Levels in AFB1-treated Chicken Hepatocytes.

569

Values are represented as means ± SEM from three experiments (n=3). Groups

570

were compared by a 1-way ANOVA followed by Duncan’s multiple range tests. Within the

571

groups without AFB1 treatment, bars with * are significantly different from the control cells

572

(P < 0.05). Within the groups with 0.05µg/ml AFB1 treatment, bars with # are significantly

573

different from the control cells (P < 0.05).

574 575

Fig. 5 Effect of SeMet on the mRNA Levels of CYP450 3A37 (A) and 1A5 (B) in

576

AFB1-treated Chicken Hepatocytes.

577

Values are represented as means ± SEM from three experiments (n=3). Groups

578

were compared by a 1-way ANOVA followed by Duncan’s multiple range tests. Within the

579

groups without AFB1 treatment, bars with * are significantly different from the control cells

580

(P < 0.05). Within the groups with 0.05µg/ml AFB1 treatment, bars with # are significantly

581

different from the control cells (P < 0.05). Significant changes are indicated by & in

582

comparison between treated cells and untreated cells by 0.05µg/ml AFB (P < 0.05).

583 584

Fig. 6 Effect of SelW Knockdown on the mRNA Level of SelW (A), Cell Viability (B)

585

and LDH Activity (C) in Chicken Hepatocytes

586

Values are represented as means ± SEM from three experiments (n=3). Groups

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were compared by a 1-way ANOVA followed by Duncan’s multiple range tests. Within the

588

groups without AFB1 treatment, bars with * are significantly different from the control cells

589

(P < 0.05). Within the groups with 0.05µg/ml AFB1 treatment, bars with # are significantly

590

different from the control cells (P < 0.05). Significant changes are indicated by & in

591

comparison between treated cells and untreated cells by 0.05µg/ml AFB (P < 0.05).

592 593

Fig. 7 Effect of SelW Knockdown on the mRNA (A) and Protein (B) Levels of CYP450

594

1A5 in Chicken Hepatocytes.

595

Values are given as means ± SEM from three experiments (n=3). Groups were

596

compared by a 1-way ANOVA followed by Duncan’s multiple range tests. Within the

597

groups with same knockdown treatment, bars with * are significantly different from the

598

control cells (P < 0.05). Significant changes are indicated by & in comparison between treated

599

cells and untreated cells by 2µM SeMet (P < 0.05).

600

601

602

603

604

605

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Tables

607

Table 1 Primers used for real-time PCR

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Product Genes

GenBank accession

Primer sequence (5′−3′) size (bp) F: TCACCATCCCGCACAGCA

CYP450 NM_205146.1

201

1A5

R: AAGTCATCACCTTCTCCGCATC F: CGAATCCCAGAAATCAGA

CYP450 NM_001001751.1 3A37

145 R: AGCCAGGTAACCAAGTGT F: CTCCGCGTCACCGTGCTC

SelW

GQ919055

150 R: CACCGTCACCTCGAACCATCCC F: TGCGTGACATCAAGGAGAAG

β-actin

NM_205518.1

300 R: TGCCAGGGTACATTGTGGTA

608

609

610

611

612

613

614

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TOC

616

617

618

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Fig. 1 Effects of Various Concentration of AFB1 on Cell Viability (A) and LDH Activity (B) in Chicken Hepatocytes. Values are represented as means ± SEM from three experiments (n=3). Groups were compared by one-way ANOVA followed by Duncan’s multiple range tests. Asterisk means values were significantly different from the control (P < 0.05).

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Fig. 2 Protective Effect of SeMet on Cell Viability (A) and LDH Activity (B) in AFB1-treated Chicken Hepatocytes Values are represented as means ± SEM from three experiments (n=3). Groups were compared by a 1-way ANOVA followed by Duncan’s multiple range tests. Within the groups without AFB1 treatment, bars with * are significantly different from the control cells (P < 0.05). Within the groups with 0.05µg/ml AFB1 treatment, bars with # are significantly different from the control cells (P < 0.05). Significant changes are indicated by & in comparison between treated cells and untreated cells by 0.05µg/ml AFB (P < 0.05).

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Fig. 3 Effect of SeMet on GSH (A), MDA (B) and SOD (C) Levels in AFB1-treated Chicken Hepatocytes Values are represented as means ± SEM from three experiments (n=3). Groups were compared by a 1-way ANOVA followed by Duncan’s multiple range tests. Within the groups without AFB1 treatment, bars with * are significantly different from the control cells (P < 0.05). Within the groups with 0.05µg/ml AFB1 treatment, bars with # are significantly different from the control cells (P < 0.05). Significant changes are indicated by & in comparison between treated cells and untreated cells by 0.05µg/ml AFB (P < 0.05).

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Fig. 4 Effect of SeMet on SelW mRNA Levels in AFB1-treated Chicken Hepatocytes. Values are represented as means ± SEM from three experiments (n=3). Groups were compared by a 1-way ANOVA followed by Duncan’s multiple range tests. Within the groups without AFB1 treatment, bars with * are significantly different from the control cells (P < 0.05). Within the groups with 0.05µg/ml AFB1 treatment, bars with # are significantly different from the control cells (P < 0.05).

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Fig. 5 Effect of SeMet on the mRNA Levels of CYP450 3A37 (A) and 1A5 (B) in AFB1-treated Chicken Hepatocytes. Values are represented as means ± SEM from three experiments (n=3). Groups were compared by a 1-way ANOVA followed by Duncan’s multiple range tests. Within the groups without AFB1 treatment, bars with * are significantly different from the control cells (P < 0.05). Within the groups with 0.05µg/ml AFB1 treatment, bars with # are significantly different from the control cells (P < 0.05). Significant changes are indicated by & in comparison between treated cells and untreated cells by 0.05µg/ml AFB (P < 0.05).

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Fig. 6 Effect of SelW Knockdown on the mRNA Level of SelW (A), Cell Viability (B) and LDH Activity (C) in Chicken Hepatocytes Values are represented as means ± SEM from three experiments (n=3). Groups were compared by a 1-way ANOVA followed by Duncan’s multiple range tests. Within the groups without AFB1 treatment, bars with * are significantly different from the control cells (P < 0.05). Within the groups with 0.05µg/ml AFB1 treatment, bars with # are significantly different from the control cells (P < 0.05). Significant changes are indicated by & in comparison between treated cells and untreated cells by 0.05µg/ml AFB (P < 0.05).

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Fig. 7 Effect of SelW Knockdown on the mRNA (A) and Protein (B) Levels of CYP450 1A5 in Chicken Hepatocytes. Values are given as means ± SEM from three experiments (n=3). Groups were compared by a 1-way ANOVA followed by Duncan’s multiple range tests. Within the groups with same knockdown treatment, bars with * are significantly different from the control cells (P < 0.05). Significant changes are indicated by & in comparison between treated cells and untreated cells by 2µM SeMet (P < 0.05).

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