Effects of nanosilver exposure on cholinesterase activities, CD41, and CDF/LIF-like expression in zebraFish (Danio rerio) larvae

BioMed Research International

Volumn 2013, Issue , 2013, Pages

  Myrzakhanova, Marzhan ^a,b   Gambardella, Chiara ^b   Falugi, Carla ^b   Gatti, Antonietta M ^c   Tagliafierro, Grazia ^b   Ramoino, Paola ^b   Bianchini, Paolo ^d   Diaspro, Alberto ^d  

^a SH UALIKHANOV KOKSHETAU STATE UNIVERSITY   (Kazakhstan)

^b UNIVERSITY OF GENOA   (Italy)

^c Nanodiagnostics Srl   (Italy)

^d ISTITUTO ITALIANO DI TECNOLOGIA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

CHOLINESTERASE; FIBRINOGEN RECEPTOR; SILVER NANOPARTICLE; GLYCOPROTEIN IIB; LEUKEMIA INHIBITORY FACTOR; LIF PROTEIN, ZEBRAFISH; METAL NANOPARTICLE; SILVER; ZEBRAFISH PROTEIN;

ARTICLE; BODY HEIGHT; CELLULAR DISTRIBUTION; CHOLINERGIC SYSTEM; CONCENTRATION (PARAMETERS); CONTROLLED STUDY; DOSE RESPONSE; EMBRYO; EMBRYO DEATH; ENZYME ACTIVITY; ENZYME LOCALIZATION; IMMUNE SYSTEM; IMMUNOREACTIVITY; LARVA; LETHALITY; MORTALITY; NONHUMAN; PARTICLE SIZE; PRE T LYMPHOCYTE; PROTEIN EXPRESSION; RISK FACTOR; ZEBRA FISH; ANIMAL; CHEMICALLY INDUCED; DRUG EFFECTS; ENZYME ACTIVATION; FEMALE; METABOLISM; PREGNANCY; PRENATAL EXPOSURE; SURVIVAL RATE; TOXICITY; CHEMICALLY INDUCED DISORDER; DRUG EFFECT;

ANIMALS; CHOLINESTERASES; DOSE-RESPONSE RELATIONSHIP, DRUG; ENZYME ACTIVATION; FEMALE; LARVA; LEUKEMIA INHIBITORY FACTOR; METAL NANOPARTICLES; PLATELET MEMBRANE GLYCOPROTEIN IIB; PREGNANCY; PRENATAL EXPOSURE DELAYED EFFECTS; SILVER; SURVIVAL RATE; ZEBRAFISH; ZEBRAFISH PROTEINS;

EID: 84883202929     PISSN: 23146133     EISSN: 23146141     Source Type: Journal    
DOI: 10.1155/2013/205183     Document Type: Article

References (60)

1. Pulit J., Banach M., Kowalski Z., Nanosilver-making difficult decisions. The International Council on Nanotechnologies 2011 18 2 185 195
2. Vaidyanathan R., Kalishwaralal K., Gopalram S., Gurunathan S., Nanosilver-The burgeoning therapeutic molecule and its green synthesis. Biotechnology Advances 2009 27 6 924 937 2-s2.0-70349781652 10.1016/j. biotechadv.2009.08.001
3. Cheng D., Yang J., Zhao Y., Antibacterial materials of silver nanoparticles application in medical appliances and appliances for daily use. Chinese Medical Equipment Journal 2004 4 26 32
4. Zhang Y.-Y., Sun J., A study on the bio-safety for nano-silver as anti-bacterial materials. Chinese Journal of Medical Instrumentation 2007 31 1 36 38 2-s2.0-84856277410
5. Johnston H. J., Hutchison G., Christensen F. M., Peters S., Hankin S., Stone V., A review of the in vivo and in vitro toxicity of silver and gold particulates: particle attributes and biological mechanisms responsible for the observed toxicity. Critical Reviews in Toxicology 2010 40 4 328 346 2-s2.0-77949780454 10.3109/10408440903453074
6. Ahamed M., AlSalhi M. S., Siddiqui M. K. J., Silver nanoparticle applications and human health. Clinica Chimica Acta 2010 411 23-24 1841 1848 2-s2.0-77957753618 10.1016/j.cca.2010.08.016
7. Ellman G. L., Courtney K. D., Andres V. Jr., Featherstone R. M., A new and rapid colorimetric determination of acetylcholinesterase activity. Biochemical Pharmacology 1961 7 2 88 95 2-s2.0-33644811612
8. Dockery D. W., Pope C. A. III, Xu X., Spengler J. D., Ware J. H., Fay M. E., Ferris B. G. Jr., Speizer F. E., An association between air pollution and mortality in six U.S. cities. The New England Journal of Medicine 1993 329 24 1753 1759 2-s2.0-0027362097 10.1056/NEJM199312093292401
9. Bar-Ilan O., Albrecht R. M., Fako V. E., Furgeson D. Y., Toxicity assessments of multisized gold and silver nanoparticles in zebrafish embryos. Small 2009 5 16 1897 1910 2-s2.0-69049115300 10.1002/smll.200801716
10. Griffitt R. J., Hyndman K., Denslow N. D., Barber D. S., Comparison of molecular and histological changes in zebrafish gills exposed to metallic nanoparticles. Toxicological Sciences 2009 107 2 404 415 2-s2.0-59149102096 10.1093/toxsci/kfn256
11. Falugi C., Aluigi M. G., Chiantore M. C., Privitera D., Ramoino P., Gatti M. A., Fabrizi A., Pinsino A., Matranga V., Toxicity of metal oxide nanoparticles in immune cells of the sea urchin. Marine Environmental Research 2012 76 114 121 2-s2.0-84858997393 10.1016/j.marenvres.2011.10.003
12. Panyala N. R., Peña-Méndez E. M., Havel J., Silver or silver nanoparticles: a hazardous threat to the environment and human health? Journal of Applied Biomedicine 2008 6 3 117 129 2-s2.0-56549119606
13. Klippstein R., Fernandez-Montesinos R., Castillo P. M., Zaderenko A. P., Pozo D., Silver nanoparticles interactions with the immune system: implications for health and disease. Silver Nanoparticles 2010 chapter 16 309 324
14. Kushima Y., Hatanaka H., Interleukin-6 and leukemia inhibitory factor promote the survival of acetylcholinesterase-positive neurons in culture from embryonic rat spinal cord. Neuroscience Letters 1992 143 1-2 110 114 2-s2.0-0026658025
15. Metcalf D., Hilton D., Nicola N. A., Leukemia inhibitory factor can potentiate murine megakaryocyte production in vitro. Blood 1991 77 10 2150 2153 2-s2.0-0025862329
16. Gao W., Thompson L., Zhou Q., Putheti P., Fahmy T. M., Strom T. B., Metcalfe S. M., Treg versus Th17 lymphocyte lineages are cross-regulated by LIF versus IL-6. Cell Cycle 2009 8 9 1444 1450 2-s2.0-65949124869
17. Myrzakhanov N., Myrzakhanova M. N., On development of The lymph and blood of dogs in the protein composition under some effects on organisms. European Scientific Journal 2013 9 6 1857 7881
18. Myrzakhanova M. N., Khanturin M. R., Nurgaliyeva K. B., Effects of adrenaline and acetylcholine on the contractile activity of venous isolated strips of lower vertebrates. News of Academy of Sciences 1997
19. Nurgaliyeva K. B., Myrzakhanova M. N., Lakpayeva S. G., Reflex shifts of hemo- and lymphodynamics during sciatic nerve stimulation in lower vertebrates. Research 1995 5 44 49. Russian
20. Nieto-Cerón S., Del Campo L. F. S., Muñoz-Delgado E., Vidal C. J., Campoy F. J., Muscular dystrophy by merosin deficiency decreases acetylcholinesterase activity in thymus of Lama2dy mice. Journal of Neurochemistry 2005 95 4 1035 1046 2-s2.0-28244492010 10.1111/j.1471-4159.2005. 03433.x
21. Sánchez del Campo L. F., Nieto-Cerón S., Morote-García J. C., Muñoz-Delgado E., Vidal C. J., Campoy F. J., Butyrylcholinesterase activity and molecular components in thymus of healthy and merosin-deficient Lama2dy mice. Neurochemistry International 2007 50 3 531 539 2-s2.0-33846631413 10.1016/j.neuint.2006.11.001
22. Bertrand J. Y., Kim A. D., Teng S., Traver D., CD41+ cmyb+ precursors colonize the zebrafish pronephros by a novel migration route to initiate adult hematopoiesis. Development 2008 135 10 1853 1862 2-s2.0-49449098431 10.1242/dev.015297
23. Gambardella C., Aluigi M. G., Ferrando S., Gallus L., Ramoino P., Gatti A. M., Rottigni M., Falugi C., Developmental abnormalities and changes in cholinesterase activity in sea urchin embryos and larvae from sperm exposed to engineered nanoparticles. Aquatic Toxicology 2013 130-131 77 85
24. Lennette E. D. A., An improved mounting medium for immunofluorescence microscopy. American Journal of Clinical Pathology 1978 69 6 647 648 2-s2.0-0017976546
25. Karnovsky M. J., Roots L., A direct-coloring thiocholine method for cholinesterases. The Journal of Histochemistry and Cytochemistry 1964 12 219 221 2-s2.0-78651153462
26. Sturm A., Da Silva De Assis H. C., Hansen P.-D., Cholinesterases of marine teleost fish: enzymological characterization and potential use in the monitoring of neurotoxic contamination. Marine Environmental Research 1999 47 4 389 398 2-s2.0-0032996160 10.1016/S0141-1136(98)00127-5
27. Sistrom C. L., Garvan C. W., Proportions, odds, and risk. Radiology 2004 230 1 12 19 2-s2.0-0346218110 10.1148/radiol.2301031028
28. Underwood A. J., Experiments in Ecology: Their Logical Design and Interpretation Using Analysis of Variance 1997 Cambridge, UK Cambridge University Press
29. Hammer Ø., Harper D. A. T., Ryan P. D., Past: Paleontological statistics software package for education and data analysis. Palaeontologia Electronica 2001 4 1 1 9 2-s2.0-34748886657
30. Meeker N. D., Trede N. S., Immunology and zebrafish: spawning new models of human disease. Developmental and Comparative Immunology 2008 32 7 745 757 2-s2.0-40849097610 10.1016/j.dci.2007.11.011
31. Lubick N., Nanosilver toxicity: ions, nanoparticles-or both? Environmental Science & Technology 2008 42 23 8617 2-s2.0-61549136692 10.1021/es8026314
32. Massoulie J., Pezzementi L., Bon S., Krejci E., Vallette F.-M., Molecular and cellular biology of cholinesterases. Progress in Neurobiology 1993 41 1 31 91 2-s2.0-0027318577 10.1016/0301-0082(93)90040-Y
33. Falugi C., Localization and possible role of molecules associated with the cholinergic system during "non-nervous" developmental events. European Journal of Histochemistry 1993 37 4 287 294 2-s2.0-0027145654
34. Soreq H., Seidman S., Acetylcholinesterase-new roles for an old actor. Nature Reviews Neuroscience 2001 2 4 294 302 2-s2.0-0035320772 10.1038/35067589
35. Gilboa-Geffen A., Hartmann G., Soreq H., Stressing hematopoiesis and immunity: an acetylcholinesterase window into nervous and immune system interactions. Frontiers in Molecular Neuroscience 2012 5 30 2-s2.0-84859307724 10.3389/fnmol.2012.00030
36. Rosas-Ballina M., Olofsson P. S., Ochani M., Valdés-Ferrer S. I., Levine Y. A., Reardon C., Tusche M. W., Pavlov V. A., Andersson U., Chavan S., Mak T. W., Tracey K. J., Acetylcholine-synthesizing T cells relay neural signals in a vagus nerve circuit. Science 2011 334 6052 98 101 2-s2.0-80053593864 10.1126/science.1209985
37. Zhang X. J., Yang L., Zhao Q., Caen J. P., He H. Y., Jin Q. H., Guo L. H., Alemany M., Zhang L. Y., Shi Y. F., Induction of acetylcholinesterase expression during apoptosis in various cell types. Cell Death and Differentiation 2002 9 8 790 800 2-s2.0-0036024019 10.1038/sj.cdd.4401034
38. Drews U., Cholinesterase in embryonic development. Progress in Histochemistry and Cytochemistry 1975 7 3 1 52 2-s2.0-0016420686
39. Falugi C., Aluigi M. G., Early appearance and possible functions of non-neuromuscular cholinesterase activities. Frontiers in Molecular Neuroscience 2012 5 54 2-s2.0-84859333946 10.3389/fnmol.2012.00054
40. Ofek K., Krabbe K. S., Evron T., Debecco M., Nielsen A. R., Brunnsgaad H., Yirmiya R., Soreq H., Pedersen B. K., Cholinergic status modulations in human volunteers under acute inflammation. Journal of Molecular Medicine 2007 85 11 1239 1251 2-s2.0-35448939247 10.1007/s00109-007-0226-x
41. Mesulam M.-M., Guillozet A., Shaw P., Levey A., Duysen E. G., Lockridge O., Acetylcholinesterase knockouts establish central cholinergic pathways and can use butyrylcholinesterase to hydrolyze acetylcholine. Neuroscience 2002 110 4 627 639 2-s2.0-0037012468 10.1016/S0306-4522(01)00613-3
42. Zimring J. C., Kapp L. M., Yamada M., Wess J., Kapp J. A., Regulation of CD8+ cytolytic T lymphocyte differentiation by a cholinergic pathway. Journal of Neuroimmunology 2005 164 1-2 66 75 2-s2.0-20644439539 10.1016/j.jneuroim.2005. 03.018
43. Falugi C., Histochemical localization of acetylcholinesterase in blood cells. Basic and Applied Histochemistry 1985 29 2 105 113 2-s2.0-0021884871
44. Topilko A., Caillou B., Acetylcholinesterase in human thymus cells. Blood 1985 66 4 891 895 2-s2.0-0021927748
45. Chang C. C., Rahmawaty A., Chang Z. W., Molecular and immunological responses of the giant freshwater prawn, Macrobrachium rosenbergii, to the organophosphorus insecticide, trichlorfon. Aquatic Toxicology 2013 130-131 18 26
46. Shifrin H., Nadler-Milbauer M., Shoham S., Weinstock M., Rivastigmine alleviates experimentally induced colitis in mice and rats by acting at central and peripheral sites to modulate immune responses. PLoS One 2013 8, article e57668 2
47. Koelle G. B., Rickard K. K., Ruch G. A., Interrelationships between ganglionic acetylcholinesterase and nonspecific cholinesterase of the cat and rat. Proceedings of the National Academy of Sciences of the United States of America 1979 76 11 6012 6016 2-s2.0-0018689464
48. Wessler I., Kilbinger H., Bittinger F., Unger R., Kirkpatrick C. J., The non-neuronal cholinergic system in humans: expression, function and pathophysiology. Life Sciences 2003 72 18-19 2055 2061 2-s2.0-0037470640 10.1016/S0024-3205(03)00083-3
49. Aluigi M. G., Guida C., Falugi C., Apoptosis as a specific biomarker of diazinon toxicity in NTera2-D1 cells. Chemico-Biological Interactions 2010 187 1-3 299 303 2-s2.0-77955509666 10.1016/j.cbi.2010.03.031
50. Dionne V. E., Stevens C. F., Voltage dependence of agonist effectiveness at the frog neuromuscular junction: resolution of a paradox. Journal of Physiology 1975 251 2 245 270 2-s2.0-0016824042
51. Sussman J. L., Harel M., Frolow F., Oefner C., Goldman A., Toker L., Silman I., Atomic structure of acetylcholinesterase from Torpedo californica: a prototypic acetylcholine-binding protein. Science 1991 253 5022 872 879 2-s2.0-0025778840
52. Maharshak N., Shenhar-Tsarfaty S., Aroyo N., MicroRNA-132 modulates cholinergic signaling and inflammation in human inflammatory bowel disease. Inflammatory Bowel Disease 2013 19 1 1346 1353
53. Zanini D., Schmatz R., Pelinson L. P., Pimentel V. C., da Costa P., Cardoso A. M., Martins C. C., Schetinger C. C., Baldissareli J., do Carmo Araújo M., Oliveira L., Chiesa J., Morsch V. M., Leal D. B., Schetinger M. R., Ectoenzymes and cholinesterase activity and biomarkers of oxidative stress in patients with lung cancer. Molecular Cell Biochemistry 2013 374 1-2 137 148
54. Kumar K., Ansari B. A., Malathion toxicity: skeletal deformities in zebrafish (Brachydanio rerio, Cyprinidae). Pesticide Science 1984 15 2 107 111
55. Sultatos L. G., Mammalian toxicology of organophosphorus pesticides. Journal of Toxicology and Environmental Health 1994 43 3 271 289 2-s2.0-0028149404
56. Shapira M., Grant A., Korner M., Soreq H., Genomic and transcriptional characterization of the human ACHE locus: complex involvement with acquired and inherited diseases. The Israel Medical Association Journal 2000 2 6 470 473 2-s2.0-0033839348
57. Falugi C., Rakonczay Z., Thielecke H., Guida C., Aluigi M.G., Aluigi. cholinergic pesticides. 2010, http://cdn.intechopen.com/pdfs/13230/InTech- Cholinergic-pesticides.pdf
58. Suliman Y. A. O., Ali D., Alarifi S., Harrath A. H., Mansour L., Alwasel S. H., Evaluation of cytotoxic, oxidative stress, proinflammatory and genotoxic effect of silver nanoparticles in human lung epithelial cells. Environmental Toxicology 2013 10.1002/tox.21880
59. Sailaja B. S., Cohen-Carmon D., Zimmerman G., Soreq H., Meshorer E., Stress-induced epigenetic transcriptional memory of acetylcholinesterase by HDAC4. Proceedings of the National Academy of Science 2012 109 52 E3687 E3695
60. Chen X., Schluesener H. J., Nanosilver: a nanoproduct in medical application. Toxicology Letters 2008 176 1 1 12 2-s2.0-37049000154 10.1016/j.toxlet.2007.10.004