Cuprizone [Bis(Cyclohexylidenehydrazide)] is Selectively Toxic for Mature Oligodendrocytes

被引:115
作者
Benardais, Karelle [1 ,2 ]
Kotsiari, Alexandra [1 ]
Skuljec, Jelena [1 ,2 ]
Koutsoudaki, Paraskevi N. [1 ,2 ]
Gudi, Viktoria [1 ]
Singh, Vikramjeet [1 ,2 ]
Vulinovic, Franca [1 ]
Skripuletz, Thomas [1 ]
Stangel, Martin [1 ,2 ]
机构
[1] Hannover Med Sch, Dept Neurol, Clin Neuroimmunol & Neurochem, D-30625 Hannover, Germany
[2] Ctr Syst Neurosci, Hannover, Germany
关键词
In vitro; Cuprizone; Oligodendrocytes; Mitochondrial transmembrane potential; Demyelination; CELL-CULTURES; REMYELINATION; DEMYELINATION; NEUROTOXICANT; DEGENERATION; COPPER; MATTER; WHITE; BRAIN; GREY;
D O I
10.1007/s12640-013-9380-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Cuprizone [bis(cyclohexylidenehydrazide)]-induced toxic demyelination is an experimental animal model commonly used to study de- and remyelination in the central nervous system. In this model, mice are fed with the copper chelator cuprizone which leads to oligodendrocyte death with subsequent demyelination. The underlying mechanisms of cuprizone-induced oligodendrocyte death are still unknown, and appropriate in vitro investigations to study these mechanisms are not available. Thus, we studied cuprizone effects on rat primary glial cell cultures and on the neuroblastoma cell line SH-SY5Y. Treatment of cells with different concentrations of cuprizone failed to show effects on the proliferation and survival of SH-SY5Y cells, microglia, astrocytes, and oligodendrocyte precursor cells (OPC). In contrast, differentiated mature oligodendrocytes (OL) were found to be significantly affected by cuprizone treatment. This was accompanied by a reduced mitochondrial potential in cuprizone-treated OL. These results demonstrate that the main toxic target for cuprizone is mature OL, whilst other glial cells including OPC are not or only marginally affected. This explains the selective demyelination induced by cuprizone in vivo.
引用
收藏
页码:244 / 250
页数:7
相关论文
共 20 条
[1]   Cuprizone neurotoxicity, copper deficiency and neurodegeneration [J].
Benetti, Federico ;
Ventura, Marcello ;
Salmini, Benedetta ;
Ceola, Stefano ;
Carbonera, Donatella ;
Mammi, Stefano ;
Zitolo, Andrea ;
D'Angelo, Paola ;
Urso, Emanuela ;
Maffia, Michele ;
Salvato, Benedetto ;
Spisni, Enzo .
NEUROTOXICOLOGY, 2010, 31 (05) :509-517
[2]   DEMYELINATION OF SUPERIOR CEREBELLAR PEDUNCLE IN MOUSE INDUCED BY CUPRIZONE [J].
BLAKEMORE, WF .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1973, 20 (01) :63-72
[3]   OBSERVATIONS ON OLIGODENDROCYTE DEGENERATION, RESOLUTION OF STATUS SPONGIOSUS AND REMYELINATION IN CUPRIZONE INTOXICATION IN MICE [J].
BLAKEMORE, WF .
JOURNAL OF NEUROCYTOLOGY, 1972, 1 (04) :413-426
[4]   The neurotoxicant, cuprizone, retards the differentiation of oligodendrocytes in vitro [J].
Cammer, W .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1999, 168 (02) :116-120
[5]  
CARLTON WILLIAM W., 1967, LIFE SCI, V6, P11, DOI 10.1016/0024-3205(67)90356-6
[6]  
Denic Aleksandar, 2011, Pathophysiology, V18, P21, DOI 10.1016/j.pathophys.2010.04.004
[7]   Mitochondria and apoptosis [J].
Green, DR ;
Reed, JC .
SCIENCE, 1998, 281 (5381) :1309-1312
[8]   Regional differences between grey and white matter in cuprizone induced demyelination [J].
Gudi, Viktoria ;
Moharregh-Khiabani, Darius ;
Skripuletz, Thomas ;
Koutsoudaki, Paraskevi N. ;
Kotsiari, Alexandra ;
Skuljec, Jelena ;
Trebst, Corinna ;
Stangel, Martin .
BRAIN RESEARCH, 2009, 1283 :127-138
[9]   DECREASE IN OLIGODENDROCYTE CARBONIC-ANHYDRASE ACTIVITY PRECEDING MYELIN DEGENERATION IN CUPRIZONE INDUCED DEMYELINATION [J].
KOMOLY, S ;
JEYASINGHAM, MD ;
PRATT, OE ;
LANTOS, PL .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1987, 79 (1-2) :141-148
[10]   Chronic toxic demyelination in the central nervous system leads to axonal damage despite remyelination [J].
Lindner, Maren ;
Fokuhl, Jantje ;
Linsmeier, Franziska ;
Trebst, Corinna ;
Stangel, Martin .
NEUROSCIENCE LETTERS, 2009, 453 (02) :120-125