Effect of endocrine disrupting chemicals on the transcription of genes related to the innate immune system in the early developmental stage of zebrafish (Danio rerio)

Fish and Shellfish Immunology

Volumn 28, Issue 5-6, 2010, Pages 854-861

  Jin, Yuanxiang ^a   Chen, Rujia ^a   Liu, Weiping ^a   Fu, Zhengwei ^a  

^a ZHEJIANG UNIVERSITY OF TECHNOLOGY   (China)

Author keywords

Cytokines; Endocrine disrupting chemicals; Gene transcription; Innate immune system; Zebrafish

Indexed keywords

DANIO RERIO;

EID: 77951124613     PISSN: 10504648     EISSN: 10959947     Source Type: Journal    
DOI: 10.1016/j.fsi.2010.02.009     Document Type: Article

References (62)

1. Mills L.J., and Chichester C. Review of evidence: are endocrine-disrupting chemicals in the aquatic environment impacting fish populations?. Sci Total Environ 43 (2005) 1-34
2. Propper C.R. The study of endocrine-disrupting compounds: past approaches and new directions. Integr Comp Biol 45 (2005) 194-200
3. Harrad S., Ibarra C., Robson M., Melymuk L., Zhang X., Diamond M., et al. Polychlorinated biphenyls in domestic dust from Canada, New Zealand, United Kingdom and United States: implications for human exposure. Chemosphere 76 (2009) 232-238
4. McKinlay R., Plant J.A., Bell J.N.B., and Voulvoulis N. Endocrine disrupting pesticides: implications for risk assessment. Environ Int 34 (2008) 168-183
5. Colborn T., vom Saal F.S., and Soto A.M. Developmental effects of endocrine-disrupting chemicals in wildlife and humans. Environ Health Perspect 101 (1993) 378-384
6. Mann D.R., Ansari A.A., Akinbami M.A., Wallen K., Gould K.G., and McClure H.M. Neonatal treatment with luteinizing hormone-releasing hormone analogs alters peripheral lymphocyte subsets and cellular and humorally mediated immune responses in juvenile and adult male monkeys. J Clin Endocrinol Metab 78 (1994) 292-298
7. Ahmed S.A. The immune system as a potential target for environmental estrogens (endocrine disrupters): a new emerging field. Toxicology 150 (2000) 191-206
8. Lutton B., and Callard I. Evolution of reproductive immune interactions. Integr Comp Biol 46 (2006) 1060-1071
9. Staples J.E., Fiore N.C., Frazier Jr. D.E., Gasiewicz T.A., and Silverstone A.E. Overexpression of the anti-apoptotic oncogene, bcl-2, in the thymus does not prevent thymic atrophy induced by estradiol or 2,3,7,8-tetrachlorodibenzop-dioxin. Toxicol Appl Pharmacol 151 (1998) 200-210
10. Banerjee B.D., Koner B.C., and Ray A. Influence of stress on DDT-induced humoral immune responsiveness in mice. Environ Res 74 (1997) 43-47
11. Chapin R.E., Harris M.W., Davis B.J., Ward S.M., Wilson R.E., Mauney M.A., et al. The effects of perinatal: juvenile methoxychlor exposure on adult rat nervous, immune, and reproductive system function. Fundam Appl Toxicol 40 (1997) 138-157
12. Secombes C.J., Zou J., Laing K., Daniels G.D., and Cunningham C. Cytokine genes in fish. Aquaculture 172 (1999) 93-102
13. Sullivan C., and Kim C.H. Zebrafish as a model for infectious disease and immune function. Fish Shellfish Immunol 25 (2008) 341-350
14. Rojo I., de Ilárduya O.M., Estonba A., and Pardo M.A. Innate immune gene expression in individual zebrafish after Listonella anguillarum inoculation. Fish Shellfish Immunol 23 (2007) 1285-1293
15. Hermann A.C., and Kim C.H. Effects of arsenic on zebrafish innate immune system. Mar Biotechnol 7 (2005) 494-505
16. Desbrow C., Routledge E.J., Brighty G.C., Sumpter J.P., and Waldock M. Identification of estrogenic chemicals in STW effluent. 1. Chemical fractionation and in vitro biological screening. Environ Sci Technol 32 (1998) 1549-1558
17. Filby A.L., Neuparth T., Thorpe K.L., Owen R., Galloway T.S., and Tyler C.R. Health impacts of estrogens in the environment, considering complex mixture effects. Environ Health Perspect 115 (2007) 1704-1710
18. Go V., Garey J., Wolff M.S., and Pogo B.G.T. Estrogenic potential of certain pyrethroid compounds in the MCF-7 human breast carcinoma cell line. Environ Health Perspect 107 (1999) 173-177
19. Perry M.J., Venners S.A., Barr B.D., and Xu X. Environmental pyrethroid and organophosphorus insecticide exposures and sperm concentration. Reprod Toxicol 23 (2007) 113-118
20. Jin Y.X., Wang W.Y., Xu C., Fu Z.W., and Liu W.P. Induction of hepatic estrogen-responsive gene transcription by permethrin enantiomers in male adult zebrafish. Aquat Toxicol 88 (2008) 146-152
21. Petit F., Le Goff P., Cravedi J.P., Valotaire Y., and Pakdel F. Two complementary bioassays for screening the estrogenic potency of xenobiotics: recombinant yeast for trout estrogen receptor and trout hepatocyte cultures. J Mol Endocrinol 19 (1997) 321-335
22. Spanò L., Tyler C.R., van Aerle R., Devos P., Mandiki S.N.M., Silvestre F., et al. Effects of atrazine on sex steroid dynamics, plasma vitellogenin concentration and gonad development in adult goldfish (Carassius auratus). Aquat Toxicol 66 (2004) 369-379
23. Salaberria I., Hansen B.H., Asensio V., Olsvik P.A., Andersen R.A., and Jenssen B.M. Effects of atrazine on hepatic metabolism and endocrine homeostasis in rainbow trout (Oncorhynchus mykiss). Toxicol Appl Pharmacol 234 (2009) 98-106
24. Andreassen T.K., Skjoedt K., and Korsgaard B. Upregulation of estrogen receptor α and vitellogenin in eelpout (Zoarces viviparus) by waterborne exposure to 4-tert-octylphenol and 17β-estradiol. Comp Biochem Phys C 140 (2005) 340-346
25. Yang F.X., Xu Y., and Hui Y. Reproductive effects of prenatal exposure to nonylphenol on zebrafish (Danio rerio). Comp Biochem Phys C 142 (2006) 77-84
26. Hill R.L., and Janz D.M. Developmental estrogenic exposure in zebrafish (Danio rerio): I. Effects on sex ratio and breeding success. Aquat Toxicol 63 (2003) 417-429
27. Seki M., Yokota H., Maeda M., Tadokoro H., and Kobayashi K. Effects of 4-nonylphenol and 4-tert-octylphenol on sex differentiation and vitellogenin induction in medaka (Oryzias latipes). Environ Toxicol Chem 22 (2003) 1507-1516
28. Flynn K., and Spellman T. Environmental levels of atrazine decrease spatial aggregation in the fresh water mussel, Elliptio complanata. Ecotoxicol Environ Saf 72 (2009) 1228-1233
29. Thorpe K.L., Gross-Sorokin M., Johnson I., Brighty G., and Tyler C.R. An assessment of the model of concentration addition for predicting the estrogenic activity of chemical mixtures in wastewater treatment works effluents. Environ Health Perspect 114 (2006) 90-97
30. Brian J.V., Harris C.A., Scholze M., Kortenkamp A., Booy P., Lamoree M., et al. Evidence of estrogenic mixture effects on the reproductive performance of fish. Environ Sci Technol 41 (2007) 337-344
31. Filby A.L., Santos E.M., Thorpe K.L., Maack G., and Tyler C.R. Gene expression profiling for understanding chemical causation of biological effects for complex mixtures: a case study on estrogens. Environ Sci Technol 41 (2007) 8187-8194
32. Bayne C.J., and Gerwick L. The acute phase response and innate immunity of fish. Dev Comp Immunol 25 (2001) 725-743
33. Phelan P.E., Pressley M.E., Witten P.E., Mellon M.T., Blake S.L., and Kim C.H. Characterization of snakehead rhabdovirus infection of zebrafish (Danio rerio). J Virol 79 (2004) 1842-1852
34. Stockhammer O.W., Zakrzewska A., Hegedûs Z., Spaink H.P., and Meijer A.H. Transcriptome profiling and functional analyses of the zebrafish embryonic innate immune response to Salmonella infection. J Immunol 182 (2009) 5641-5653
35. Westerfield M. The zebrafish book: a guide for the laboratory use of zebrafish Danio (Brachydanio) rerio (1993), University of Oregon Press
36. -ΔΔCt method. Methods 25 (2001) 402-408
37. Watzke J., Schirmer K., and Scholz S. Bacterial lipopolysaccharides induce genes involved in the innate immune response in embryos of the zebrafish (Danio rerio). Fish Shellfish Immunol 23 (2007) 901-905
38. Nayak A.S., Lage C.R., and Kim C.H. Effects of low concentrations of arsenic on the innate immune system of the zebrafish (Danio rerio). Toxicol Sci 98 (2007) 118-124
39. Trede N.S., Langenau D.M., Traver D., Look A.T., and Zon L.I. The use of zebrafish to understand immunity. Immunity 20 (2004) 367-379
40. Lam S.H., Chua H.L., Gong Z., Lam T.J., and Sin Y.M. Development and maturation of the immune system in zebrafish, Danio rerio: a gene expression profiling, in situ hybridization and immunological study. Dev Comp Immunol 28 (2004) 9-28
41. Eder K.J., Clifford M.A., Hedrick R.P., Köhler H.R., and Werner I. Expression of immune-regulatory genes in juvenile Chinook salmon following exposure to pesticides and infectious hematopoietic necrosis virus (IHNV). Fish Shellfish Immunol 25 (2008) 508-516
42. Dinarello C.A. Biologic basis for interleukin-1 in disease. Blood 87 (1996) 2095-2147
43. So T., Lee S.W., and Croft M. Tumor necrosis factor/tumor necrosis factor receptor family members that positively regulate immunity. Int J Hematol 83 (2006) 1-11
44. Baggiolini M., Dewald B., and Moser B. Interleukin-8 and related chemotactic cytokines-CXC and CC chemokines. Adv Immunol 55 (1994) 97-179
45. Canesi L., Lorusso L.C., Ciacci C., Betti M., Rocchi M., Pojana G., et al. Immunomodulation of Mytilus hemocytes by individual estrogenic chemicals and environmentally relevant mixtures of estrogens: in vitro and in vivo studies. Aquat Toxicol 81 (2007) 36-44
46. Williams T.D., Diab A.M., George S.G., Sabine V., and Chipman J.K. Gene expression responses of European flounder (Platichthys flesus) to 17-β estradiol. Toxicol Lett 168 (2007) 236-248
47. Eells J.T., Rasmussen J.L., Bandettini P.A., and Propp J.M. Differences in the neuroexcitatory actions of pyrethroid insecticides and sodium channel-specific neurotoxins in rat and trout brain synaptosomes. Toxicol Appl Pharmacol 123 (1993) 107-119
48. Singh A., and Srivastava V.K. Toxic effect of synthetic pyrethroid permethrin on the enzyme system of the freshwater fish Channa striatus. Chemosphere 39 (1999) 1951-1956
49. González-Doncel M., de la Peña E., Barrueco C., and Hinton D.E. Stage sensitivity of medaka (Oryzias latipes) eggs and embryos to permethrin. Aquat Toxicol 62 (2003) 255-268
50. Ribardo D.A., Kuhl K.R., Boldogh I., Peterson J.W., Houston C.W., and Chopra A.K. Early cell signaling by the cytotoxic enterotoxin of Aeromonas hydrophila in macrophages. Microb Pathog 32 (2002) 149-163
51. Chen T., Zhao X.Y., Liu Y., Shi Q., Hua Z.C., and Shen P.P. Analysis of immunomodulating nitric oxide, iNOS and cytokines mRNA in mouse macrophages induced by microcystin-LR. Toxicology 197 (2004) 67-77
52. Giardina T.M., Steer J.H., Lo S.Z., and Joyce D.A. Uncoupling protein-2 accumulates rapidly in the inner mitochondrial membrane during mitochondrial reactive oxygen stress in macrophages. Biochim Biophys Acta Bioenerg 1777 (2008) 118-129
53. Hockenbery D.M., Oltvai Z.N., Yin X.M., Milliman C.L., and Korsmeyer S.J. Bcl-2 functions in an antioxidant pathway to prevent apoptosis. Cell 75 (1993) 241-251
54. Nègre-Salvayre A., Hirtz C., Carrera G., Cazenave R., Troly M., Salvayre R., et al. A role for uncoupling protein-2 as a regulator of mitochondrial hydrogen peroxide generation. FASEB J 11 (1997) 809-815
55. Echtay K.S., Roussel D., St-Pierre J., Jekabsons M.B., Cadenas S., Stuart J.A., et al. Superoxide activates mitochondrial uncoupling proteins. Nature 415 (2002) 96-99
56. Deng J., Yu L., Liu C., Yu K., Shi X., Yeung L.W., et al. Hexabromocyclododecane-induced developmental toxicity and apoptosis in zebrafish embryos. Aquat Toxicol 93 (2009) 29-36
57. Karpuzoglu E., and Ahmed S.A. Estrogen regulation of nitric oxide and inducible nitric oxide synthase (iNOS) in immune cells: implications for immunity, autoimmune diseases, and apoptosis. Nitric Oxide 15 (2006) 177-186
58. Kim P.K., Zamora R., Petrosko P., and Billiar T.R. The regulatory role of nitric oxide in apoptosis. Int Immunopharmacol 1 (2001) 1421-1441
59. Nathan C. Nitric oxide as a secretory product of mammalian cells. FASEB J 6 (1992) 3051-3064
60. Tafalla C., Coll J., and Secombes C.J. Expression of genes related to the early immune response in rainbow trout (Oncorhynchus mykiss) after viral haemorrhagic septicemia virus (VHSV) infection. Dev Comp Immunol 29 (2005) 615-626
61. Rodríguez I., Chamorro R., Novoa B., and Figueras A. β-Glucan administration enhances disease resistance and some innate immune responses in zebrafish (Danio rerio). Fish Shellfish Immunol 27 (2009) 369-373
62. Rodríguez I., Figueras A., and Novoa B. Immune response of zebrafish (Danio rerio) against a newly isolated bacterial pathogen Aeromonas hydrophila. Fish Shellfish Immunol 25 (2008) 239-249