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

  • Yoon Seong Jang
  • , Mun Yong Lee
  • , Sung Ho Choi
  • , Mi Young Kim
  • , Hemin Chin
  • , Seong Whan Jeong
  • , In Kyung Kim
  • , Oh Joo Kwon
  • The Catholic University of Korea
  • PetaGen Inc.
  • National Institutes of Health

Research output: Contribution to journalArticlepeer-review

10 Scopus citations

Abstract

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.

Original languageEnglish
Pages (from-to)203-211
Number of pages9
JournalBrain Research
Volume999
Issue number2
DOIs
StatePublished - 5 Mar 2004

Bibliographical note

Funding Information:
This study was supported by the KOSEF through the Cell Death Disease Center of MRC at The Catholic University of Korea (R13-2002-005-01003-0) (S.-W. Jeong).

Keywords

  • Endoplasmic reticulum
  • Immunohistochemistry
  • Neurotoxicity

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