Activation of protein kinase C-δ attenuates kainate-induced cell death of cortical neurons

被引:15
|
作者
Jung, YS
Lee, BK
Park, HS
Shim, JK
Kim, SU
Lee, SH
Baik, EJ
Moon, CH [1 ]
机构
[1] Ajou Univ, Dept Physiol, Suwon 442749, Kyungkido, South Korea
[2] Ajou Univ, Brain Dis Res Sch, Sch Med, Suwon 442749, Kyungkido, South Korea
关键词
cortical neurons; kainate; protein kinase c-delta;
D O I
10.1097/00001756-200505120-00017
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We investigated the role of individual protein kinase C (PKC) isoforms during kainate toxicity in cortical neurons. Treatment with 50 mu M kainate induced isoform-specific activation of PKC-delta according to the translocation from the soluble to the particulate fraction, while it caused remarkable decreases in PKC alpha, beta, epsilon and zeta in both fractions. Kainate-induced neuronal death was significantly increased by pharmacological inhibition of PKC-delta with rottlerin, suggesting a protective role of PKC-delta against kainate toxicity. A PKC activator phorbol 12-myristate 13-acetate remarkably attenuated the kainate-induced neuronal death. Although phorbol 12-myristate 13-acetate activates PKC-epsilon and PKC-delta, the protective effect of phorbol 12-myristate 13-acetate was almost completely abolished by rottlerin, but not by epsilon VI-2. These results suggest that activation of PKC-delta attenuates the kainate-induced cell death of cortical neurons. NeuroReport 16:741-744 (c) 2005 Lippincott Williams & Wilkins.
引用
收藏
页码:741 / 744
页数:4
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