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British Journal of Pharmacology
Article . 2000 . Peer-reviewed
License: Wiley Online Library User Agreement
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DIGITAL.CSIC
Article . 2013 . Peer-reviewed
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Induction of COX‐2 and PGE2 biosynthesis by IL‐1β is mediated by PKC and mitogen‐activated protein kinases in murine astrocytes

Authors: Molina-Holgado, E.; Ortiz, Sergio; Molina-Holgado, F.; Guaza, Carmen;

Induction of COX‐2 and PGE2 biosynthesis by IL‐1β is mediated by PKC and mitogen‐activated protein kinases in murine astrocytes

Abstract

Interleukin‐1 (IL‐1) is an important mediator of immunoinflammatory responses in the brain. In the present study, we examined whether prostaglandin E2 (PGE2) production after IL‐1β stimulation is dependent upon activation of protein kinases in astroglial cells. Astrocyte cultures stimulated with IL‐1β or the phorbol ester, PMA significantly increased PGE2 secretion. The stimulatory action of IL‐1β on PGE2 production was totally abolished by NS‐398, a specific inhibitor of cyclo‐oxygenase‐2 activity, as well as by the protein synthesis inhibitor cycloheximide, and the glucocorticoid dexamethasone. Furthermore, IL‐1β induced the expression of COX‐2 mRNA. This occurred early at 2 h, with a maximum at 4 h and declined at 12 h. IL‐1 β treatment also induced the expression of COX‐2 protein as determined by immunoblot analysis. In that case the expression of the protein remained high at least up to 12 h. Treatment of cells with protein kinase C inhibitors (H‐7, bisindolylmaleimide and calphostin C) inhibited IL‐1β stimulation of PGE2. In addition, PKC‐depleted astrocyte cultures by overnight treatment with PMA no longer responded to PMA or IL‐1. The ablation of the effects of PMA and IL‐1β on PGE2 production, likely results from down‐regulation of phorbol ester sensitive‐PKC isoenzymes. Immunoblot analysis demonstrated the translocation of the conventional isoform cPKC‐α from cytosol to membrane following treatment with IL‐1β. In addition, IL‐1β treatment led to activation of extracellular signal‐regulated kinase (ERK1/2) and p38 subgroups of MAP kinases in astroglial cells. Interestingly, the inhibition of ERK kinase with PD 98059, as well as the inhibition of p38 MAPK with SB 203580, prevented IL‐1β‐induced PGE2 release. ERK1/2 activation by IL‐1β was sensitive to inhibition by the PKC inhibitor bisindolylmaleimide suggesting that ERK phosphorylation is a downstream signal of PKC activation. These results suggest key roles for PKC as well as for ERK1/2 and p38 MAP kinase cascades in the biosynthesis of PGE2, likely by regulating the induction of cyclo‐oxygenase‐2, in IL‐1β‐stimulated astroglial cells. British Journal of Pharmacology (2000) 131, 152–159; doi:10.1038/sj.bjp.0703557

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Spain
Keywords

Mice, Inbred BALB C, p38 Mitogen-Activated Protein Kinases, Dinoprostone, Isoenzymes, Mice, Cyclooxygenase 2, Prostaglandin-Endoperoxide Synthases, Astrocytes, Enzyme Induction, Animals, Mitogen-Activated Protein Kinases, Cells, Cultured, Protein Kinase C, Interleukin-1, Signal Transduction

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
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