BDNF and NT-3 but not CNTF counteract the Ca2+ ionophore-induced apoptosis of cultured cortical neurons:: involvement of dual pathways

被引:28
作者
Takei, N
Tanaka, O
Endo, Y
Lindholm, D
Hatanaka, H
机构
[1] Niigata Univ, Brain Res Inst, Dept Mol Neurobiol, Niigata 9518585, Japan
[2] Osaka Univ, Inst Prot Res, Div Protein Biosynth, Suita, Osaka 5650871, Japan
[3] Uppsala Univ, Biomed Ctr, Dept Dev Neurosci, Uppsala, Sweden
[4] Kyoto Inst Technol, Dept Appl Biol, Kyoto 6060962, Japan
关键词
BDNF; NT-3; apoptosis; Ca2+ ionophore; PI3; kinase; MAP kinase;
D O I
10.1016/S0028-3908(98)00189-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The effect of neurotrophic factors on apoptosis induced by ionomycin, a potent Ca2+ ionophore, was investigated using cultured cortical neurons from embryonic rats. Brain-derived neurotophic factor (BDNF) and neurotrophin-3 (NT-3) prevented the ionomycin-mediated cell death in a dose-dependent manner. In contrast to the neurotrophins, cilliary neurotrophic factor (CNTF) did not rescue neurons from cell death induced by ionomycin. The protective effect of BDNF was partially blocked by wortmannin, a phosphatidylinositol 3-kinase inhibitor, and by PD98059, a MAP kinase kinase inhibitor. However, the addition of both compounds together completely inhibited the survival promoting effect of BDNF. These results suggest that the neuroprotective effect of BDNF requires activation of both phosphatidylinositol-3 kinase and the Ras/MAP kinase cascade and that CNTF signaling through other pathways is without an effect in this system. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:283 / 288
页数:6
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