Abstract
The transcription factor NF-κB is activated in neurons and promotes neuronal death in cerebral ischemia. Its target genes include cytosolic phospholipase A-2 (cPLA-2), cyclooxygenase-2 (COX-2), and microsomal prostaglandin E2 synthase-1 (mPGES-1), three genes that are involved in the synthesis of prostaglandin E2 (PGE2). In our study, oxygen glucose deprivation (OGD), an in vitro model of cerebral ischemia, activated NF-κB activity in primary cortical neurons. Furthermore, OGD and the NF-κB activator tumor necrosis factor stimulated the expression of cPLA-2, cyclooxygenase-2 (COX-2), and mPGES-1 and increased the release of PGE2 from neurons. Expression of a constitutively active IκB kinase (IKK) or the NF-κB subunit p65 in neurons stimulated the transcription of cPLA-2, COX-2, and mPGES-1. Finally, inhibition of IKK in neurons blocked the induction of the three genes involved in PGE2 synthesis in vivo. In summary, NF-κB controls the neuronal expression of three genes involved in PGE2 synthesis in cerebral ischemia.
| Original language | English |
|---|---|
| Journal | Naunyn-Schmiedeberg's Archives of Pharmacology |
| Volume | 380 |
| Issue number | 2 |
| Pages (from-to) | 153-160 |
| Number of pages | 8 |
| ISSN | 0028-1298 |
| DOIs | |
| Publication status | Published - 01.08.2009 |
Funding
Acknowledgment This work was supported by a grant from Deutsche Forschungsgemeinschaft (Schw 416/5-1). WB was funded by the Egyptian Ministry for Higher Education. We thank Dr. Hiroaki Naraba, Iwate Medical University, Japan for providing mPGES-luc.
Research Areas and Centers
- Academic Focus: Center for Brain, Behavior and Metabolism (CBBM)