Expression of B/K protein in the hippocampus of kainate-induced rat seizure model

被引:9
|
作者
Jang, YS
Lee, MY
Choi, SH
Kim, MY
Chin, H
Jeong, SW
Kim, IK
Kwon, OJ
机构
[1] Catholic Univ Korea, Coll Med, Dept Biochem, Seoul 137701, South Korea
[2] Catholic Univ Korea, Coll Med, Dept Anat, Seoul 137701, South Korea
[3] PetaGen Inc, R&D Ctr, Seoul 120140, South Korea
[4] NEI, NIH, Bethesda, MD 20892 USA
关键词
immunohistochemistry; neurotoxicity; endoplasmic reticulum;
D O I
10.1016/j.brainres.2003.11.047
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
B/K protein is a newly identified member of double C2-like domain protein family. We examined the expression of B/K protein in the hippocampus of kainate-induced rat seizure model. Intraperitoneal injection of kainate increased the immunoreactivity to B/K protein in the CA1 to CA3 of the hippocampus. B/K protein expression began to increase at 6 h, reached the maximum at 12 h, and then returned nearly to the normal level at 72 h after the injection of kainate (12 mg/kg), and it was also dependent on the dose of kainate between 4 and 16 mg/kg. In electron microscopic and subcellular fractionation studies, B/K protein was localized in the endoplasmic reticulum (ER) of the hippocampus. Kainate also induced the expression of BiP, a typical ER stress marker protein, in the hippocampus and the cortex, and it was coexpressed with B/K protein. Moreover, thapsigargin-induced ER stress caused upregulation of B/K protein expression in PC12 cells. In conclusion, our data showing the induction of both B/K protein expression and ER stress response in the hippocampus of kainate seizure model, and ER-specific expression and ER stress-induced expression of B/K strongly suggest the possible role of B/K protein in epileptogenesis or epilepsy-induced neuronal damage. Published by Elsevier B.V.
引用
收藏
页码:203 / 211
页数:9
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