Calcium ionophores can induce either apoptosis or necrosis in cultured cortical neurons

被引:115
作者
Gwag, BJ
Canzoniero, LMT
Sensi, SL
Demaro, JA
Koh, JY
Goldberg, MP
Jacquin, M
Choi, DW [1 ]
机构
[1] Ajou Univ, Sch Med, Dept Pharmacol, Suwon 442749, Kyungkido, South Korea
[2] Washington Univ, Sch Med, Dept Neurol, St Louis, MO 63110 USA
[3] Washington Univ, Sch Med, Ctr Study Nervous Syst Injury, St Louis, MO 63110 USA
[4] Univ Ulsan, Sch Med, Dept Neurol, Seoul, South Korea
关键词
cortical neurons; calcium ionophore; apoptosis; necrosis; BDNF; IGF-I;
D O I
10.1016/S0306-4522(98)00508-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Cultured cortical neurons exposed for 24 h to low concentrations of the Ca2+ ionophores, ionomycin (250 nM) or A-23187 (100 nM), underwent apoptosis, accompanied by early degeneration of neurites, cell body shrinkage, chromatin condensation and internucleosomal DNA fragmentation. This death could be blocked by protein synthesis inhibitors, as well as by the growth factors brain-derived neurotrophic factor or insulin-like growth factor I. If the ionomycin concentration was increased to 1-3 mu M, then neurons underwent necrosis, accompanied by early cell body swelling without DNA laddering, or sensitivity to cycloheximide or growth factors. Calcium imaging with Fura-2 suggested a possible basis for the differential effects of low and high concentrations of ionomycin. At low concentrations, ionomycin induced greater increases in intracellular Ca2+ concentration in neurites than in neuronal cell bodies, whereas at high concentrations, ionomycin produced large increases in intracellular Ca2+ concentration in both neurites and cell bodies. We hypothesize that the ability of low concentrations of Ca2+ ionophores to raise intracellular Ca2+ concentration preferentially in neurites caused early neurite degeneration, leading to loss of growth factor availability to the cell body and consequent apoptosis, whereas high concentrations of ionophores produced global cellular Ca2+ overload and consequent necrosis. (C) 1999 IBRO. Published by Elsevier Science Ltd.
引用
收藏
页码:1339 / 1348
页数:10
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