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Protein kinases and prostaglandin production in ovine astroglia.
- Source :
-
Prostaglandins [Prostaglandins] 1995 Jul; Vol. 50 (1), pp. 33-45. - Publication Year :
- 1995
-
Abstract
- We examined the effects of interleukin-1 alpha (IL-1 alpha) and involvement of protein kinases on prostaglandin production in cultured ovine astroglia. Ovine astroglia were exposed to media alone, or 10 ng/mL IL-1 alpha and prostaglandin F2 alpha (PGF2 alpha) levels were analyzed using enzyme immunoassay. Application of IL-1 alpha augmented the production of PGF2 alpha at 4 h. Coapplication of H-7 (10-1000 microM) and staurosporine (0.1-10 microM), inhibitors of protein kinase C (PKC), blocked IL-1 alpha-induced PGF2 alpha production. IL-1 alpha increased cyclooxygenase (COX) activity while coapplication of staurosporine prevented an increase, implying that COX activity was dependent upon PKC activation. In contrast, forskolin, sodium nitroprusside, and cyclic nucleotide analogs alone did not affect prostaglandin production significantly, excluding the involvement of cAMP/cGMP-dependent protein kinases. Coapplication of quinacrine (10 microM) and bromophenacyl bromide (100 microM), inhibitors of phospholipase A2 (PLA2), prevented the IL-1 alpha-induced increases in PGF2 alpha production. Lastly, IL-1 alpha increased labeled arachidonic acid (AA) release whereas coaddition of quinacrine (10 microM) attenuated increased AA release. Therefore, we propose that IL-1 alpha enhances prostaglandin production by ovine astroglia via steps involving activation of PKC and increased activity of COX and PLA2.
- Subjects :
- Animals
Arachidonic Acid metabolism
Astrocytes cytology
Cells, Cultured
Cyclic AMP-Dependent Protein Kinases drug effects
Cyclic AMP-Dependent Protein Kinases metabolism
Cyclic AMP-Dependent Protein Kinases physiology
Cyclic GMP-Dependent Protein Kinase Type I
Cyclic GMP-Dependent Protein Kinases drug effects
Cyclic GMP-Dependent Protein Kinases metabolism
Cyclic GMP-Dependent Protein Kinases physiology
Dinoprost analysis
Dinoprost biosynthesis
Enzyme Activation
Interleukin-1 pharmacology
Phospholipases A physiology
Phospholipases A2
Prostaglandin-Endoperoxide Synthases drug effects
Prostaglandin-Endoperoxide Synthases metabolism
Prostaglandins A metabolism
Protein Kinase C drug effects
Protein Kinase C metabolism
Protein Kinase C physiology
Receptors, Interleukin-1 antagonists & inhibitors
Receptors, Interleukin-1 physiology
Sheep
Astrocytes metabolism
Prostaglandins biosynthesis
Protein Kinases physiology
Subjects
Details
- Language :
- English
- ISSN :
- 0090-6980
- Volume :
- 50
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Prostaglandins
- Publication Type :
- Academic Journal
- Accession number :
- 8588070
- Full Text :
- https://doi.org/10.1016/0090-6980(95)00087-q