Induction of oxiapoptophagy, a mixed mode of cell death associated with oxidative stress, apoptosis and autophagy, on 7-ketocholesterol-treated 158N murine oligodendrocytes: Impairment by α-tocopherol

Biochemical and Biophysical Research Communications

Volumn 446, Issue 3, 2014, Pages 714-719

  Nury, Thomas ^a   Zarrouk, Amira ^a,b   Vejux, Anne ^a   Doria, Margaux ^a   Riedinger, Jean Marc ^c   Delage Mourroux, Régis ^d   Lizard, Gérard ^a  

^a Faculté des Sciences Gabriel   (France)

^b UNIVERSITY OF MONASTIR   (Tunisia)

^c Centre de Lutte Contre le Cancer GF Leclerc   (France)

^d UNIVERSITÉ DE FRANCHE COMTÉ   (France)

Author keywords

158N cells; 7 Ketocholesterol; Apoptosis; Autophagy; Oxiapoptophagy; Oxidative stress; Tocopherol

Indexed keywords

7 OXOCHOLESTEROL; ACRIDINE ORANGE; ALPHA TOCOPHEROL; CASPASE 3; HYDROETHIDINE; MICROTUBULE ASSOCIATED PROTEIN; PROPIDIUM IODIDE; REACTIVE OXYGEN METABOLITE;

ANIMAL CELL; ANIMAL EXPERIMENT; APOPTOSIS; ARTICLE; AUTOPHAGY; CELL ACTIVATION; CELL DEATH; CELL ORGANELLE; CELL STRUCTURE; LIGHT CHAIN; MEMBRANE PERMEABILITY; MURINAE; NONHUMAN; OLIGODENDROGLIA; OXIAPOPTOPHAGY; OXIDATIVE STRESS; PRIORITY JOURNAL; STAINING;

158N CELLS; 7-KETOCHOLESTEROL; APOPTOSIS; AUTOPHAGY; OXIAPOPTOPHAGY; OXIDATIVE STRESS; Α-TOCOPHEROL;

ALPHA-TOCOPHEROL; ANIMALS; APOPTOSIS; AUTOPHAGY; CELL DEATH; CELLS, CULTURED; DOSE-RESPONSE RELATIONSHIP, DRUG; KETOCHOLESTEROLS; MICE; MICROSCOPY, PHASE-CONTRAST; MICROTUBULE-ASSOCIATED PROTEINS; OLIGODENDROGLIA; OXIDATIVE STRESS;

EID: 84898825859     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2013.11.081     Document Type: Article

References (28)

1. W.J. Griffiths, P.J. Crick, and Y. Wang Methods for oxysterol analysis: past, present and future Biochem. Pharmacol. 86 2013 3 14
2. L. Iuliano Pathways of cholesterol oxidation via non-enzymatic mechanisms Chem. Phys. Lipids 164 2011 457 468
3. A. Vejux, and G. Lizard Cytotoxic effects of oxysterols associated with human diseases: induction of cell death (apoptosis and/or oncosis), oxidative and inflammatory activities, and phospholipidosis Mol. Aspects Med. 30 2009 153 170
4. G. Poli, F. Biasi, and G. Leonarduzzi Oxysterols in the pathogenesis of major chronic diseases Redox Biol. 1 2013 125 130
5. Q. Zhou, E. Wasowicz, B. Handler, B. Handler, L. Fleischer, and F.A. Kummerow An excess concentration of oxysterols in the plasma is cytotoxic to cultured endothelial cells Atherosclerosis 149 2000 191 197
6. S.M. Colles, J.M. Maxson, S.G. Carlson, and G.M. Chisolm Oxidized LDL-induced injury and apoptosis in atherosclerosis. Potential roles for oxysterols Trends Cardiovasc. Med. 11 2001 131 138
7. I.R. Rodríguez, and I.M. Larrayoz Cholesterol oxidation in the retina: implications of 7KCh formation in chronic inflammation and age-related macular degeneration J. Lipid Res. 51 2010 2847 2862
8. D. Cheng, A.M. Jenner, G. Shui, W.F. Cheong, T.W. Mitchell, J.R. Nealon, W.S. Kim, H. McCann, M.R. Wenk, G.M. Halliday, and B. Garner Lipid pathway alterations in Parkinson's disease primary visual cortex PLoS One 6 2 2011 e17299
9. V. Leoni, T. Masterman, F.S. Mousavi, B. Wretlind, L.O. Wahlund, U. Diczfalusy, J. Hillert, and I. Björkhem Diagnostic use of cerebral and extracerebral oxysterols Clin. Chem. Lab. Med. 42 2004 186 191
10. M. Baarine, P. Andréoletti, A. Athias, T. Nury, A. Zarrouk, K. Ragot, A. Vejux, J.M. Riedinger, Z. Kattan, G. Bessede, D. Trompier, S. Savary, M. Cherkaoui-Malki, and G. Lizard Evidence of oxidative stress in very long chain fatty acid-treated oligodendrocytes and potentialization of ROS production using RNA interference-directed knockdown of ABCD1 and ACOX1 peroxisomal proteins Neuroscience 213 2012 1 18
11. K. Ragot, J.J. Mackrill, A. Zarrouk, T. Nury, V. Aires, A. Jacquin, A. Athias, J.P. Pais de Barros, A. Véjux, J.M. Riedinger, D. Delmas, and G. Lizard Absence of correlation between oxysterol accumulation in lipid raft microdomains, calcium increase, and apoptosis induction on 158N murine oligodendrocytes Biochem. Pharmacol. 86 2013 67 79
12. S. Monier, M. Samadi, C. Prunet, M. Denance, A. Laubriet, A. Athias, A. Berthier, E. Steinmetz, G. Jürgens, A. Nègre-Salvayre, G. Bessède, S. Lemaire-Ewing, D. Néel, P. Gambert, and G. Lizard Impairment of the cytotoxic and oxidative activities of 7 beta- hydroxycholesterol and 7-ketocholesterol by esterification with oleate Biochem. Biophys. Res. Commun. 303 2003 814 824
13. A. Vejux, S. Guyot, T. Montange, J.M. Riedinger, E. Kahn, and G. Lizard Phospholipidosis and down-regulation of the PI3-K/PDK-1/Akt signalling pathway are vitamin E inhibitable events associated with 7-ketocholesterol-induced apoptosis J. Nutr. Biochem. 20 2009 45 61
14. J.H. Son, J.H. Shim, K.H. Kim, J.Y. Ha, and J.Y. Han Neuronal autophagy and neurodegenerative diseases Exp. Mol. Med. 44 2012 89 98
15. M. Baarine, K. Ragot, E.C. Genin, H. El Hajj, D. Trompier, P. Andreoletti, M.S. Ghandour, F. Menetrier, M. Cherkaoui-Malki, S. Savary, and G. Lizard Peroxisomal and mitochondrial status of two murine oligodendrocytic cell lines (158N, 158JP): potential models for the study of peroxisomal disorders associated with dysmyelination processes J. Neurochem. 111 2009 119 131
16. A. Zarrouk, A. Vejux, T. Nury, H.I. El Hajj, M. Haddad, M. Cherkaoui-Malki, J.M. Riedinger, M. Hammami, and G. Lizard Induction of mitochondrial changes associated with oxidative stress on very long chain fatty acids (C22:0, C24:0, or C26:0)-treated human neuronal cells (SK-NB-E) Oxid. Med. Cell. Longev. 2012 2012 623257
17. M. Olsson, I. Rundquist, and U. Brunk Flow cytofluorometry of lysosomal acridine orange uptake by living cultured cells Acta Path. Microbiol. Immunol. Scand. (Sect A) 95 1987 159 165
18. A. Altmeyer, A.C. Jung, M. Ignat, S. Benzina, J.M. Denis, J. Gueulette, G. Noël, D. Mutter, and P. Bischoff Pharmacological enhancement of autophagy induced in a hepatocellular carcinoma cell line by high-LET radiation Anticancer Res. 30 2010 303 310
19. G. Lizard, S. Fournel, L. Genestier, N. Dhedin, C. Chaput, M. Flacher, M. Mutin, G. Panaye, and J.P. Revillard Kinetics of plasma membrane and mitochondrial alterations in cells undergoing apoptosis Cytometry 21 1995 275 283
20. S. Lemaire-Ewing, C. Prunet, T. Montange, A. Vejux, A. Berthier, G. Bessède, L. Corcos, P. Gambert, D. Néel, and G. Lizard Comparison of the cytotoxic, pro-oxidant and pro-inflammatory characteristics of different oxysterols Cell. Biol. Toxicol. 21 2005 97 114
21. W. Martinet, D.M. Schrijvers, J.P. Timmermans, and H. Bult Interactions between cell death induced by statins and 7-ketocholesterol in rabbit aorta smooth muscle cells Br. J. Pharmacol. 154 2008 1236 1246
22. C. He, H. Zhu, W. Zhang, I. Okon, Q. Wang, H. Li, Y.Z. Le, and Z. Xie 7-Ketocholesterol induces autophagy in vascular smooth muscle cells through Nox4 and Atg4B Am. J. Pathol. 183 2013 626 637
23. M. Xu, X.X. Li, J. Xiong, M. Xia, E. Gulbins, Y. Zhang, and P.L. Li Regulation of autophagic Flux by dynein-mediated autophagosomes trafficking in mouse coronary arterial myocytes Biochim. Biophys. Acta 2013 pii: S0167-4889(13)00337-6
24. G. Jia, G. Cheng, and D.K. Agrawal Autophagy of vascular smooth muscle cells in atherosclerotic lesions Autophagy 3 2007 63 64
25. X.M. Yuan, W. Li, U.T. Brunk, H. Dalen, Y.H. Chang, and A. Sevanian Lysosomal destabilization during macrophage damage induced by cholesterol oxidation products Free Radic. Biol. Med. 28 2000 208 218
26. C. Miguet-Alfonsi, C. Prunet, S. Monier, G. Bessède, S. Lemaire-Ewing, A. Berthier, F. Ménétrier, D. Néel, P. Gambert, and G. Lizard Analysis of oxidative processes and of myelin figures formation before and after the loss of mitochondrial transmembrane potential during 7beta-hydroxycholesterol and 7-ketocholesterol-induced apoptosis: comparison with various pro-apoptotic chemicals Biochem. Pharmacol. 64 2002 527 541
27. L. Galluzzi, and G. Kroemer Necroptosis: a specialized pathway of programmed necrosis Cell 135 2008 1161 1163
28. W. Chaabane, S.D. User, M. El-Gazzah, R. Jaksik, E. Sajjadi, J. Rzeszowska-Wolny, and M.J. Los Autophagy, apoptosis, mitoptosis and necrosis: interdependence between those pathways and effects on cancer Arch. Immunol. Ther. Exp. (Warsz) 61 2013 43 58