Effects of selenium-lead interaction on the gene expression of inflammatory factors and selenoproteins in chicken neutrophils

Ecotoxicology and Environmental Safety

Volumn 139, Issue , 2017, Pages 447-453

  Li, Xiaojing ^a   Xing, Mengyuan ^a   Chen, Menghao ^a   Zhao, Jinxin ^a   Fan, Ruifeng ^a   Zhao, Xia ^a   Cao, Changyu ^a   Yang, Jie ^a   Zhang, Ziwei ^a   Xu, Shiwen ^a  

^a NORTHEAST AGRICULTURAL UNIVERSITY   (China)

Author keywords

Chicken; Inflammatory factor; Lead; Neutrophil; Selenium; Selenoprotein

Indexed keywords

BETA ACTIN; CYCLOOXYGENASE 2; GLUTATHIONE PEROXIDASE 1; GLUTATHIONE PEROXIDASE 2; GLUTATHIONE PEROXIDASE 3; IMMUNOGLOBULIN ENHANCER BINDING PROTEIN; IODOTHYRONINE; IODOTHYRONINE DEIODINASE 1; IODOTHYRONINE DEIODINASE 2; IODOTHYRONINE DEIODINASE 3; LEAD; MESSENGER RNA; METHIONINE SULFOXIDE REDUCTASE; METHIONINE SULFOXIDE REDUCTASE B1; NITRIC OXIDE SYNTHASE; PHOSPHOLIPID HYDROPEROXIDE GLUTATHIONE PEROXIDASE; SELENIUM; SELENOPROTEIN; SELENOPROTEIN F; SELENOPROTEIN I; SELENOPROTEIN K; SELENOPROTEIN S; SELENOPROTEIN T; SELENOPROTEIN W; THIOREDOXIN REDUCTASE; THIOREDOXIN REDUCTASE 1; THIOREDOXIN REDUCTASE 2; THIOREDOXIN REDUCTASE 3; TUMOR NECROSIS FACTOR; UNCLASSIFIED DRUG; UNINDEXED DRUG; AUTACOID;

BIRD; ECOTOXICOLOGY; GENE EXPRESSION; LEAD; POLLUTION EFFECT; PROTEIN; SELENIUM;

ANIMAL CELL; ANIMAL MODEL; ARTICLE; CELL ISOLATION; CHEMICAL INTERACTION; CONTROLLED STUDY; DIO1 GENE; DIO2 GENE; DIO3 GENE; ENZYME ACTIVATION; FOOD INTAKE; GENE EXPRESSION; GPX1 GENE; GPX2 GENE; GPX3 GENE; GPX4 GENE; IMMUNOCOMPETENT CELL; LEAD BLOOD LEVEL; LEAD POISONING; MALE; NEUTROPHIL; NONHUMAN; PRINCIPAL COMPONENT ANALYSIS; PROTEIN BLOOD LEVEL; PROTEIN EXPRESSION; PROTEIN PROTEIN INTERACTION; SELENIUM BLOOD LEVEL; SELH GENE; SELI GENE; SELK GENE; SELM GENE; SELN1 GENE; SELO GENE; SELPP1 GENE; SELS GENE; SELT GENE; SELU GENE; SELW1 GENE; SEP15 GENE; SEPX1 GENE; SIGNAL TRANSDUCTION; SPS2 GENE; SUPPLEMENTATION; TOXICITY TESTING; TXNRD1 GENE; TXNRD2 GENE; TXNRD3 GENE; ANIMAL; BLOOD; CHICKEN; DRUG EFFECTS; DRUG INTERACTION; GENETICS; IMMUNOLOGY; METABOLISM;

AVES; GALLUS GALLUS;

ANIMALS; CHICKENS; DRUG INTERACTIONS; GENE EXPRESSION; INFLAMMATION MEDIATORS; LEAD; MALE; NEUTROPHILS; NF-KAPPA B; RNA, MESSENGER; SELENIUM; SELENOPROTEINS;

EID: 85012188474     PISSN: 01476513     EISSN: 10902414     Source Type: Journal    
DOI: 10.1016/j.ecoenv.2017.02.017     Document Type: Article

References (54)

1. Alatise, O.I., Schrauzer, G.N., Lead exposure: a contributing cause of the current breast cancer epidemic in Nigerian women. Biol. Trace Elem. Res. 136 (2010), 127–139.
2. Bonizzi, G., Karin, M., The two NF-κB activation pathways and their role in innate and adaptive immunity. Trends Immunol. 25 (2004), 280–288.
3. Boyne, R., Arthur, J.R., Alterations of neutrophil function in selenium-deficient cattle. J. Comp. Pathol. 89 (1979), 151–158.
4. Boyne, R., Arthur, J.R., The response of selenium-deficient mice to Candida albicans infection. J. Nutr. 116 (1986), 816–822.
5. Bradford, B.M.M., A rapid sensitive method for the quantization of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 72 (1976), 248–254.
6. Chen, S.F., et al. Caveolin-1 interacts with Derlin-1 and promotes ubiquitination and degradation of cyclooxygenase-2 via collaboration with p97 complex. J. Biol. Chem. 288 (2013), 33462–33469.
7. Chen, W., et al. Molecular cloning and sequence analysis of selenoprotein W gene and its mRNA expression patterns in response to metabolic status and cadmium exposure in goldfish, Carassius auratus. Comp. Biochem. Physiol. Part B Biochem. Mol. Biol. 184 (2015), 1–9.
8. Chen, X., et al. Selenium Deficiency Influences the Gene Expressions of Heat Shock Proteins and Nitric Oxide Levels in Neutrophils of Broilers. Biol. Trace Elem. Res. 161 (2014), 334–340.
9. Cross, A., et al. The dual effects of TNFalpha on neutrophil apoptosis are mediated via differential effects on expression of Mcl-1 and Bfl-1. Blood 111 (2008), 878–884.
10. Ettler, V., et al. ICP-MS measurements of lead isotopic ratios in soils heavily contaminated by lead smelting: tracing the sources of pollution. Anal. Bioanal. Chem. 378 (2004), 311–317.
11. Flora, S.J.S., et al. Role of Selenium in Protection against Lead Intoxication. Acta Pharmacol. Toxicol. 53 (1983), 28–32.
12. Freitas, M., Fernandes, E., Zinc, cadmium and nickel increase the activation of NF-κB and the release of cytokines from THP-1 monocytic cells. Met. Integr. Biometal Sci. 3 (2011), 1238–1243.
13. Gao, H., et al. Effects of dietary selenium against lead toxicity on mRNA levels of 25 selenoprotein genes in the cartilage tissue of broiler chicken. Biol. Trace Elem. Res. 172 (2016), 234–241.
14. Ghareeb, D.A., et al. Toxic effects of lead exposure on the brain of rats: Involvement of oxidative stress, inflammation, acetylcholinesterase, and the beneficial role of flaxseed extract. Toxicol. Environ. Chem. 92 (2010), 187–195.
15. Huang, Z., et al. The role of selenium in inflammation and immunity: from molecular mechanisms to therapeutic opportunities. Antioxid. Redox Signal. 16 (2011), 705–743.
16. Hugejiletu, H., et al. Selenium supplementation alters gene expression profiles associated with innate immunity in whole-blood neutrophils of sheep. Biol. Trace Elem. Res. 154 (2013), 28–44.
17. Jiang, Y.Y., et al. Characterization and expression of chicken selenoprotein U. Biol. Trace Elem. Res. 166 (2015), 1–9.
18. Kanuri, G., et al. Role of tumor necrosis factor α (TNFα) in the onset of fructose-induced nonalcoholic fatty liver disease in mice ☆. J. Nutr. Biochem. 22 (2011), 527–534.
19. Klaassen, C.D., Watkins, J.B., Casarett and Doull's Toxicology: The Basic Science of Poisons. 2013, McGraw-Hill.
20. Kosnett, M.J., et al. Recommendations for medical management of adult lead exposure. Environ. Health Perspect. 115 (2007), 463–471.
21. Kumar, A., et al. Effects of sub chronic lead intoxication on macrophage functions of chickens. J. Immunol. Immunopathol., 2000.
22. Li, Q., Verma, I.M., NF-κB regulation in the immune system. Nat. Rev. Immunol., 2, 2002, 975 (975).
23. Liu, J., et al. Lead affects apoptosis and related gene XIAP and smac expression in the hippocampus of developing rats. Neurochem. Res. 35 (2010), 473–479.
24. Müller, Y.M.R., et al. Behavioral impairments related to lead-induced developmental neurotoxicity in chicks. Arch. Toxikol. 82 (2008), 445–451.
25. Machado, V.S., et al. Effect of an injectable trace mineral supplement containing selenium, copper, zinc, and manganese on the health and production of lactating Holstein cows. Vet. J. 197 (2013), 451–456.
26. Nagy, G., et al. Nitric oxide, chronic inflammation and autoimmunity ☆. Immunol. Lett. 111 (2007), 1–5.
27. Othman, A.I., El, M.M.A., Role of selenium against lead toxicity in male rats. J. Biochem. Mol. Toxicol. 12 (1998), 345–349.
28. Özkan-Yılmaz, F., et al. Effects of dietary selenium of organic form against lead toxicity on the antioxidant system in Cyprinus carpio. Fish. Physiol. Biochem. 40 (2014), 355–363.
29. Pfaffl, M.W., A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res., 29, 2001, e45.
30. Pollution, A. o. t. C. P., Ores, t. H. R. W. B. b. E. o. L., 2011. Assessment of the Crops Pb Pollution and the Health Risk Were Brought by Exploitation of Lead-Zinc Ores. International Conference on Bioinformatics & Biomedical Engineering. pp. 1–5.
31. Queiroz, M.L.S., et al. Defective neutrophil function in workers occupationally exposed to lead. Pharmacol. Toxicol. 72 (1993), 73–77.
32. Sehnert, B., et al. NF-κB inhibitor targeted to activated endothelium demonstrates a critical role of endothelial NF-κB in immune-mediated diseases. Proc. Natl. Acad. Sci. USA 110 (2013), 16556–16561.
33. Shah, T.J., Walsh, S.W., Activation of NF-κB and expression of COX-2 in association with neutrophil infiltration in systemic vascular tissue of women with preeclampsia. Am. J. Obstet. Gynecol. 196 (2007), 1–8.
34. Shuang, L., et al. Protective roles of selenium on nitric oxide and the gene expression of inflammatory cytokines induced by cadmium in chicken splenic lymphocytes. Biol. Trace Elem. Res. 168 (2015), 1–9.
35. Speyer, C.L., et al. Regulatory effects of iNOS on acute lung inflammatory responses in mice. Am. J. Pathol. 163 (2003), 2319–2328.
36. Sun, G.X., et al. Effect of selenium against lead-induced damage on the gene expression of heat shock proteins and inflammatory cytokines in peripheral blood lymphocytes of chickens. Biol. Trace Elem. Res., 2016, 1–7.
37. Surh, Y.J., et al. Molecular mechanisms underlying chemopreventive activities of anti-inflammatory phytochemicals: down-regulation of COX-2 and iNOS through suppression of NF-kappa B activation. Mutat. Res. 480–481 (2001), 243–268.
38. Toan, L.Q., et al., 2014. Assessment on lead and cadmium pollution in tilapia and water spinach cultivated in Nhue River related to human health risk in Hanam.
39. Tong, X., et al. The antagonistic effect of selenium on lead toxicity Is related to the ion profile in chicken liver. Biol. Trace Elem. Res. 169 (2015), 1–9.
40. Tsiridis, V., et al. Interactive toxic effects of heavy metals and humic acids on Vibrio fischeri. Ecotoxicol. Environ. Saf. 63 (2006), 158–167.
41. Uluozlu, O.D., et al. Assessment of trace element contents of chicken products from turkey. J. Hazard. Mater. 163 (2009), 982–987.
42. Ündeg̃er, Ü., et al. Immune alterations in lead-exposed workers. Toxicology 109 (1996), 167–172.
43. Valentino, M., et al. Effects of lead on polymorphonuclear leukocyte (PMN) functions in occupationally exposed workers. Arch. Toxicol. 65 (1991), 685–688.
44. Vengris, V.E., Mar, C.J., Lead poisoning in chickens and the effect of lead on interferon and antibody production. Can. J. Comp. Med. Rev. Can. De. Med. Comp. 38 (1974), 328–335.
45. Walraven, N., et al. The lead (Pb) isotope signature, behaviour and fate of traffic-related lead pollution in roadside soils in The Netherlands. Sci. Total Environ. 472 (2014), 888–900.
46. Wei, J., et al. Lead induces COX-2 expression in glial cells in a NFAT-dependent, AP-1/NFκB-independent manner. Toxicology 325 (2014), 67–73.
47. Yao, H., et al. Selenium deficiency mainly influences the gene expressions of antioxidative selenoproteins in chicken muscles. Biol. Trace Elem. Res. 161 (2014), 318–327.
48. Yu, D., et al. Effects of dietary selenium on selenoprotein W gene expression in the chicken immune organs. Biol. Trace Elem. Res. 144 (2011), 678–687.
49. Zhang, J.L., et al. Selenium deficiency affects the mRNA expression of inflammatory factors and selenoprotein genes in the kidneys of broiler chicks. Biol. Trace Elem. Res. 171 (2015), 1–7.
50. Zhang, J.L., et al. Effects of dietary selenium deficiency or excess on gene expression of selenoprotein N in chicken muscle tissues. Biol. Trace Elem. Res. 157 (2014), 234–241.
51. Zhao, W., et al. Four endoplasmic reticulum resident selenoproteins may be related to the protection of selenium against cadmium toxicity in chicken lymphocytes. Biol. Trace Elem. Res. 161 (2014), 328–333.
52. Zhao, X., et al. Selenium deficiency influences nitric oxide and selenoproteins in pancreas of chickens. Biol. Trace Elem. Res. 161 (2014), 341–349.
53. Zhao, X., et al. Protective effects of selenium on oxidative damage and oxidative stress related gene expression in rat liver under chronic poisoning of arsenic. Food Chem. Toxicol. Int. J. Publ. Br. Ind. Biol. Res. Assoc. 58 (2013), 1–7.
54. Zhao, Y., et al. Selenium deficiency downregulates selenoproteins and suppresses immune function in chicken thymus. Biol. Trace Elem. Res. 167 (2015), 1–8.