Nano copper induced apoptosis in podocytes via increasing oxidative stress

Journal of Hazardous Materials

Volumn 241-242, Issue , 2012, Pages 279-286

  Xu, Pengjuan ^a   Xu, Jing ^a   Liu, Shichang ^a   Yang, Zhuo ^a  

^a NANKAI UNIVERSITY   (China)

Author keywords

Malondialdehyde (MDA); Nanosized copper particles; Podocyte; Reactive oxygen species (ROS); Superoxide dismutase (SOD)

Indexed keywords

COPPER PARTICLES; MALONDIALDEHYDE; PODOCYTE; REACTIVE OXYGEN SPECIES; SUPEROXIDE DISMUTASES;

ALDEHYDES; AMINO ACIDS; BROMINE COMPOUNDS; COPPER; CYTOTOXICITY; OXIDATIVE STRESS; OXYGEN; TOXICITY;

CELL DEATH;

3 (4,5 DIMETHYL 2 THIAZOLYL) 2,5 DIPHENYLTETRAZOLIUM BROMIDE; 3,4 METHYLENEDIOXYAMPHETAMINE; COPPER; HOE 33342; LIPOCORTIN 5; MALONALDEHYDE; NANOMATERIAL; REACTIVE OXYGEN METABOLITE; SUPEROXIDE DISMUTASE; TIOPRONIN;

ALDEHYDE; ANTIOXIDANT; APOPTOSIS; CONCENTRATION (COMPOSITION); COPPER; ENZYME ACTIVITY; NANOTECHNOLOGY; OXIDATION; TOXICITY; VIABILITY;

ANIMAL CELL; APOPTOSIS; ARTICLE; CELL DEATH; CELL VIABILITY; CYTOTOXICITY; ENZYME ACTIVITY; GLOMERULAR FILTRATION BARRIER; MOUSE; NONHUMAN; OXIDATIVE STRESS; PODOCYTE;

ANIMALS; APOPTOSIS; CELL LINE; CELL SURVIVAL; COPPER; DOSE-RESPONSE RELATIONSHIP, DRUG; ENVIRONMENTAL POLLUTANTS; FREE RADICAL SCAVENGERS; GLYCINE; LIPID PEROXIDATION; MALONDIALDEHYDE; MICE; NANOPARTICLES; OXIDATIVE STRESS; PODOCYTES; REACTIVE OXYGEN SPECIES; SULFHYDRYL COMPOUNDS; SUPEROXIDE DISMUTASE;

EID: 84868488887     PISSN: 03043894     EISSN: 18733336     Source Type: Journal    
DOI: 10.1016/j.jhazmat.2012.09.041     Document Type: Article

References (52)

1. Emerich D.F., Thanos C.G. Nanotechnology medicine. Expert Opin. Biol. Ther. 2003, 3:655-663.
2. Long T.C., Tajuba J., Sama P., Saleh N., Swartz C., Parker J., Hester S., Lowry G.V., Veronesi B. Nanosize titanium dioxide stimulates reactive oxygen species in brain microglia and damages neurons in vitro. Environ. Health Perspect. 2007, 115:1631-1637.
3. Mahmood M., Casciano D., Xu Y., Biris A.S. Engineered nanostructural materials for application in cancer biology and medicine. J. Appl. Toxicol. 2012, 32:10-19.
4. Bell A.T. The impact of nanoscience on heterogeneous catalysis. Science 2003, 299:1688-1691.
5. Nel A., Xia T., Madler L., Li N. Toxic potential of materials at the nanolevel. Science 2006, 311:622-627.
6. Service R.F. American Chemical Society meeting. Nanomaterials show signs of toxicity. Science 2003, 300:243.
7. Cattaneo A.G., Gornati R., Sabbioni E., Chiriva-Internati M., Cobos E., Jenkins M.R., Bernardini G. Nanotechnology and human health: risks and benefits. J. Appl. Toxicol. 2010, 30:730-744.
8. Malugin A., Ghandehari H. Cellular uptake and toxicity of gold nanoparticles in prostate cancer cells: a comparative study of rods and spheres. J. Appl. Toxicol. 2010, 30:212-217.
9. Chen J., Tan M., Nemmar A., Song W., Dong M., Zhang G., Li Y. Quantification of extrapulmonary translocation of intratracheal-instilled particles in vivo in rats: effect of lipopolysaccharide. Toxicology 2006, 222:195-201.
10. Kleinman M.T., Araujo J.A., Nel A., Sioutas C., Campbell A., Cong P.Q., Li H., Bondy S.C. Inhaled ultrafine particulate matter affects CNS inflammatory processes and may act via MAP kinase signaling pathways. Toxicol. Lett. 2008, 178:127-130.
11. Nemmar A., Hoylaerts M.F., Hoet P.H., Nemery B. Possible mechanisms of the cardiovascular effects of inhaled particles: systemic translocation and prothrombotic effects. Toxicol. Lett. 2004, 149:243-253.
12. Sharma H.S., Sharma A. Nanoparticles aggravate heat stress induced cognitive deficits blood-brain barrier disruption, edema formation and brain pathology. Prog. Brain Res. 2007, 162:245-273.
13. Kim J.S., Yoon T.J., Yu K.N., Kim B.G., Park S.J., Kim H.W., Lee K.H., Park S.B., Lee J.K., Cho M.H. Toxicity and tissue distribution of magnetic nanoparticles in mice. Toxicol. Sci. 2006, 89:338-347.
14. Guo K.P., Wang Q., Fang L. Nano-scale copper-coated graphite as anode material for lithium-ion batteries. J. Appl. Electrochem. 2002, 32:679-685.
15. Liu G., Li X., Qin B., Xing D., Guo Y., Fan R. Investigation of the mending effect and mechanism of copper nano-particles on a tribologically stressed surface. Tribology Lett. 2004, 17:961-966.
16. Meng H., Chen Z., Xing G., Yuan H., Chen C., Zhao F., Zhang C., Zhao Y. Ultrahigh reactivity provokes nanotoxicity: explanation of oral toxicity of nano-copper particles. Toxicol. Lett. 2007, 175:102-110.
17. Gomes S.I., Novais S.C., Gravato C., Guilhermino L., Scott-Fordsmand J.J., Soares A.M., Amorim M.J. Effect of Cu-nanoparticles versus one Cu-salt: analysis of stress biomarkers response in Enchytraeus albidus (Oligochaeta). Nanotoxicology 2012, 6:134-143.
18. Cioffi N., Ditaranto N., Torsi L., Picca R.A., Sabbatini L., Valentini A., Novello L., Tantillo G., Bleve-Zacheo T., Zambonin P.G. Analytical characterization of bioactive fluoropolymer ultra-thin coatings modified by copper nanoparticles. Anal. Bioanal. Chem. 2005, 381:607-616.
19. Chen Z., Meng H., Xing G., Chen C., Zhao Y., Jia G., Wang T., Yuan H., Ye C., Zhao F., Chai Z., Zhu C., Fang X., Ma B., Wan L. Acute toxicological effects of copper nanoparticles in vivo. Toxicol. Lett. 2006, 163:109-120.
20. Lei R., Wu C., Yang B., Ma H., Shi C., Wang Q., Yuan Y., Liao M. Integrated metabolomic analysis of the nano-sized copper particle-induced hepatotoxicity and nephrotoxicity in rats: a rapid in vivo screening method for nanotoxicity. Toxicol. Appl. Pharmacol. 2008, 232:292-301.
21. Kuure S., Vuolteenaho R., Vainio S. Kidney morphogenesis: cellular and molecular regulation. Mech. Dev. 2000, 92:31-45.
22. Laurens W., Battaglia C., Foglieni C., De Vos R., Malanchini B., Van Damme B., Vanrenterghem Y., Remuzzi G., Remuzzi A. Direct podocyte damage in the single nephron leads to albuminuria in vivo. Kidney Int. 1995, 47:1078-1086.
23. Shibata S., Nagase M., Yoshida S., Kawachi H., Fujita T. Podocyte as the target for aldosterone: roles of oxidative stress and Sgk1. Hypertension 2007, 49:355-364.
24. Wolf G., Chen S., Ziyadeh F.N. From the periphery of the glomerular capillary wall toward the center of disease: podocyte injury comes of age in diabetic nephropathy. Diabetes 2005, 54:1626-1634.
25. Liu S., Xu L., Zhang T., Ren G., Yang Z. Oxidative stress and apoptosis induced by nanosized titanium dioxide in PC12 cells. Toxicology 2010, 267:172-177.
26. Xia T., Kovochich M., Brant J., Hotze M., Sempf J., Oberley T., Sioutas C., Yeh J.I., Wiesner M.R., Nel A.E. Comparison of the abilities of ambient and manufactured nanoparticles to induce cellular toxicity according to an oxidative stress paradigm. Nano Lett. 2006, 6:1794-1807.
27. Liu Z., Liu S., Ren G., Zhang T., Yang Z. Nano-CuO inhibited voltage-gated sodium current of hippocampal CA1 neurons via reactive oxygen species but independent from G-proteins pathway. J. Appl. Toxicol. 2011, 31:439-445.
28. Hertel C., Terzi E., Hauser N., Jakob-Rotne R., Seelig J., Kemp J.A. Inhibition of the electrostatic interaction between beta-amyloid peptide and membranes prevents beta-amyloid-induced toxicity. Proc. Natl. Acad. Sci. U.S.A. 1997, 94:9412-9416.
29. Park J., Lim D.H., Lim H.J., Kwon T., Choi J.S., Jeong S., Choi I.H., Cheon J. Size dependent macrophage responses and toxicological effects of Ag nanoparticles. Chem. Commun. (Camb) 2011, 47:4382-4384.
30. Gao F., Horie T. A synthetic analog of prostaglandin E(1) prevents the production of reactive oxygen species in the intestinal mucosa of methotrexate-treated rats. Life Sci. 2002, 71:1091-1099.
31. Kolla N., Wei Z., Richardson J.S., Li X.M. Amitriptyline and fluoxetine protect PC12 cells from cell death induced by hydrogen peroxide. J. Psychiatry Neurosci. 2005, 30:196-201.
32. Potter T.M., Neun B.W., Stern S.T. Assay to detect lipid peroxidation upon exposure to nanoparticles. Methods Mol. Biol. 2011, 697:181-189.
33. Mitsos S.E., Fantone J.C., Gallagher K.P., Walden K.M., Simpson P.J., Abrams G.D., Schork M.A., Lucchesi B.R. Canine myocardial reperfusion injury: protection by a free radical scavenger N-2-mercaptopropionyl glycine. J. Cardiovasc. Pharmacol. 1986, 8:978-988.
34. Roco M.C. Nanotechnology: convergence with modern biology and medicine. Curr. Opin. Biotechnol. 2003, 14:337-346.
35. Sahoo S.K., Labhasetwar V. Nanotech approaches to drug delivery and imaging. Drug Discov. Today 2003, 8:1112-1120.
36. Wilkinson J.M. Nanotechnology applications in medicine. Med. Device Technol. 2003, 14:29-31.
37. Bertinato J., L'Abbe M.R. Maintaining copper homeostasis: regulation of copper-trafficking proteins in response to copper deficiency or overload. J. Nutr. Biochem. 2004, 15:316-322.
38. Zietz B.P., Dieter H.H., Lakomek M., Schneider H., Kessler-Gaedtke B., Dunkelberg H. Epidemiological investigation on chronic copper toxicity to children exposed via the public drinking water supply. Sci. Total Environ. 2003, 302:127-144.
39. Sarkar A., Das J., Manna P., Sil P.C. Nano-copper induces oxidative stress and apoptosis in kidney via both extrinsic and intrinsic pathways. Toxicology 2011, 290:208-217.
40. Holzman L.B., St John P.L., Kovari I.A., Verma R., Holthofer H., Abrahamson D.R. Nephrin localizes to the slit pore of the glomerular epithelial cell. Kidney Int. 1999, 56:1481-1491.
41. Kerjaschki D. Dysfunctions of cell biological mechanisms of visceral epithelial cell (podocytes) in glomerular diseases. Kidney Int. 1994, 45:300-313.
42. Pagtalunan M.E., Miller P.L., Jumping-Eagle S., Nelson R.G., Myers B.D., Rennke H.G., Coplon N.S., Sun L., Meyer T.W. Podocyte loss and progressive glomerular injury in type II diabetes. J. Clin. Invest. 1997, 99:342-348.
43. Mosmann T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J. Immunol. Methods 1983, 65:55-63.
44. Vega-Warner V., Ransom R.F., Vincent A.M., Brosius F.C., Smoyer W.E. Induction of antioxidant enzymes in murine podocytes precedes injury by puromycin aminonucleoside. Kidney Int. 2004, 66:1881-1889.
45. Thannickal V.J., Fanburg B.L. Reactive oxygen species in cell signaling. Am. J. Physiol. Lung Cell. Mol. Physiol. 2000, 279:L1005-L1028.
46. Martindale J.L., Holbrook N.J. Cellular response to oxidative stress: signaling for suicide and survival. J. Cell. Physiol. 2002, 192:1-15.
47. Yoshida Y., Itoh N., Saito Y., Hayakawa M., Niki E. Application of water-soluble radical initiator 2,2'-azobis[2-(2-imidazolin-2-yl)propane] dihydrochloride, to a study of oxidative stress. Free Radic. Res. 2004, 38:375-384.
48. Deres P., Halmosi R., Toth A., Kovacs K., Palfi A., Habon T., Czopf L., Kalai T., Hideg K., Sumegi B., Toth K. Prevention of doxorubicin-induced acute cardiotoxicity by an experimental antioxidant compound. J. Cardiovasc. Pharmacol. 2005, 45:36-43.
49. Paes M.C., Oliveira M.B., Oliveira P.L. Hydrogen peroxide detoxification in the midgut of the blood-sucking insect, Rhodnius prolixus. Arch. Insect Biochem. Physiol. 2001, 48:63-71.
50. Patel M. Inhibition of neuronal apoptosis by a metalloporphyrin superoxide dismutase mimic. J. Neurochem. 1998, 71:1068-1074.
51. Rothstein J.D., Bristol L.A., Hosler B., Brown R.H., Kuncl R.W. Chronic inhibition of superoxide dismutase produces apoptotic death of spinal neurons. Proc. Natl. Acad. Sci. U.S.A. 1994, 91:4155-4159.
52. Troy C.M., Shelanski M.L. Down-regulation of copper/zinc superoxide dismutase causes apoptotic death in PC12 neuronal cells. Proc. Natl. Acad. Sci. U.S.A. 1994, 91:6384-6387.